5888[geneid] - ClinVar - NCBI

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VariationLocation		Gene(s)	Protein change	Condition(s)	Clinical significance (Last reviewed)	Review status
Select item 1535961.	GRCh38/hg38 15q15.1(chr15:40581118-40720039)x1 GRCh37: Chr15:40873316-41012237 GRCh38: Chr15:40581118-40720039	KNL1, LOC129390688, LOC130056860, LOC130056861, LOC130056862, LOC130056863, LOC130056864, RAD51, RAD51-AS1, TRS-GCT4-2		See cases	Uncertain significance (Jul 22, 2013)	no assertion criteria provided
Select item 12356392.	NM_002875.5(RAD51):c.-208G>C GRCh37: Chr15:40987418 GRCh38: Chr15:40695220	RAD51		not provided	Benign (Jul 20, 2018)	criteria provided, single submitter
Select item 12607673.	NM_002875.5(RAD51):c.-207C>T GRCh37: Chr15:40987419 GRCh38: Chr15:40695221	RAD51		not provided	Benign (Jun 23, 2018)	criteria provided, single submitter
Select item 131284.	NM_002875.5(RAD51):c.-98G>C GRCh37: Chr15:40987528 GRCh38: Chr15:40695330	LOC130056864, RAD51		not provided	Benign (Jun 22, 2018)	criteria provided, single submitter
Select item 12433495.	NM_002875.5(RAD51):c.-61G>T GRCh37: Chr15:40987565 GRCh38: Chr15:40695367	LOC130056864, RAD51		not provided	Benign (Jun 22, 2018)	criteria provided, single submitter
Select item 12611766.	NM_002875.5(RAD51):c.-3+102C>T GRCh37: Chr15:40987725 GRCh38: Chr15:40695527	RAD51		not provided	Benign (Jun 22, 2018)	criteria provided, single submitter
Select item 8030707.	NM_002875.5(RAD51):c.1dup (p.Met1fs) GRCh37: Chr15:40990955-40990956 GRCh38: Chr15:40698757-40698758	RAD51	M1fs	Mirror movements 2	Uncertain significance (May 28, 2019)	criteria provided, single submitter
Select item 24626998.	NM_002875.5(RAD51):c.6A>C (p.Ala2=) GRCh37: Chr15:40990962 GRCh38: Chr15:40698764	RAD51		Inborn genetic diseases	Likely benign (Feb 28, 2023)	criteria provided, single submitter
Select item 25608419.	NM_002875.5(RAD51):c.8T>C (p.Met3Thr) GRCh37: Chr15:40990964 GRCh38: Chr15:40698766	RAD51	M3T	Inborn genetic diseases	Uncertain significance (Apr 25, 2023)	criteria provided, single submitter
Select item 176893210.	NM_002875.5(RAD51):c.9G>A (p.Met3Ile) GRCh37: Chr15:40990965 GRCh38: Chr15:40698767	RAD51	M3I	Inborn genetic diseases	Uncertain significance (Aug 7, 2022)	criteria provided, single submitter
Select item 246266011.	NM_002875.5(RAD51):c.10C>A (p.Gln4Lys) GRCh37: Chr15:40990966 GRCh38: Chr15:40698768	RAD51	Q4K	Inborn genetic diseases	Uncertain significance (Mar 11, 2023)	criteria provided, single submitter
Select item 177615912.	NM_002875.5(RAD51):c.15G>T (p.Met5Ile) GRCh37: Chr15:40990971 GRCh38: Chr15:40698773	RAD51	M5I	Inborn genetic diseases	Uncertain significance (Dec 15, 2021)	criteria provided, single submitter
Select item 179740813.	NM_002875.5(RAD51):c.28A>G (p.Asn10Asp) GRCh37: Chr15:40990984 GRCh38: Chr15:40698786	RAD51	N10D	Inborn genetic diseases	Uncertain significance (Oct 5, 2021)	criteria provided, single submitter
Select item 172994714.	NM_002875.5(RAD51):c.32C>G (p.Ala11Gly) GRCh37: Chr15:40990988 GRCh38: Chr15:40698790	RAD51	A11G	Inborn genetic diseases	Uncertain significance (Feb 1, 2022)	criteria provided, single submitter
Select item 173100515.	NM_002875.5(RAD51):c.33A>C (p.Ala11=) GRCh37: Chr15:40990989 GRCh38: Chr15:40698791	RAD51		Inborn genetic diseases	Likely benign (Jun 20, 2022)	criteria provided, single submitter
Select item 262469216.	NM_002875.5(RAD51):c.35A>G (p.Asp12Gly) GRCh37: Chr15:40990991 GRCh38: Chr15:40698793	RAD51	D12G	Inborn genetic diseases	Uncertain significance (Sep 14, 2023)	criteria provided, single submitter
Select item 174392617.	NM_002875.5(RAD51):c.48A>G (p.Glu16=) GRCh37: Chr15:40991004 GRCh38: Chr15:40698806	RAD51		Inborn genetic diseases	Likely benign (Sep 13, 2021)	criteria provided, single submitter
Select item 263694218.	NM_002875.5(RAD51):c.53_69delinsTATCTTCTT (p.Glu18fs) GRCh37: Chr15:40991009-40991025 GRCh38: Chr15:40698811-40698827	RAD51	E18fs	RAD51-related condition	Likely pathogenic (Sep 15, 2022)	criteria provided, single submitter
Select item 174854519.	NM_002875.5(RAD51):c.55A>G (p.Ser19Gly) GRCh37: Chr15:40991011 GRCh38: Chr15:40698813	RAD51	S19G	Inborn genetic diseases	Uncertain significance (Jul 17, 2021)	criteria provided, single submitter
Select item 175330520.	NM_002875.5(RAD51):c.63C>T (p.Gly21=) GRCh37: Chr15:40991019 GRCh38: Chr15:40698821	RAD51		Inborn genetic diseases	Likely benign (Jul 9, 2020)	criteria provided, single submitter
Select item 175654321.	NM_002875.5(RAD51):c.69A>G (p.Gln23=) GRCh37: Chr15:40991025 GRCh38: Chr15:40698827	RAD51		Inborn genetic diseases	Likely benign (Nov 1, 2021)	criteria provided, single submitter
Select item 175716622.	NM_002875.5(RAD51):c.70C>T (p.Pro24Ser) GRCh37: Chr15:40991026 GRCh38: Chr15:40698828	RAD51	P24S	Inborn genetic diseases	Uncertain significance (Aug 23, 2022)	criteria provided, single submitter
Select item 175716423.	NM_002875.5(RAD51):c.70C>G (p.Pro24Ala) GRCh37: Chr15:40991026 GRCh38: Chr15:40698828	RAD51	P24A	Inborn genetic diseases	Uncertain significance (Nov 30, 2021)	criteria provided, single submitter
Select item 175765124.	NM_002875.5(RAD51):c.71C>T (p.Pro24Leu) GRCh37: Chr15:40991027 GRCh38: Chr15:40698829	RAD51	P24L	Inborn genetic diseases	Uncertain significance (Oct 17, 2021)	criteria provided, single submitter
Select item 176156925.	NM_002875.5(RAD51):c.79C>T (p.Arg27Trp) GRCh37: Chr15:40991035 GRCh38: Chr15:40698837	RAD51	R27W	Inborn genetic diseases	Uncertain significance (Oct 5, 2021)	criteria provided, single submitter
Select item 176199726.	NM_002875.5(RAD51):c.80G>A (p.Arg27Gln) GRCh37: Chr15:40991036 GRCh38: Chr15:40698838	RAD51	R27Q	Inborn genetic diseases, not provided	Uncertain significance (Sep 1, 2023)	criteria provided, multiple submitters, no conflicts
Select item 133780627.	NM_002875.5(RAD51):c.80G>T (p.Arg27Leu) GRCh37: Chr15:40991036 GRCh38: Chr15:40698838	RAD51	R27L	not specified	Uncertain significance (Dec 24, 2020)	criteria provided, single submitter
Select item 176362228.	NM_002875.5(RAD51):c.84A>G (p.Leu28=) GRCh37: Chr15:40991040 GRCh38: Chr15:40698842	RAD51		Inborn genetic diseases	Likely benign (May 31, 2022)	criteria provided, single submitter
Select item 256084329.	NM_002875.5(RAD51):c.86A>G (p.Glu29Gly) GRCh37: Chr15:40991042 GRCh38: Chr15:40698844	RAD51	E29G	Inborn genetic diseases	Uncertain significance (Apr 1, 2023)	criteria provided, single submitter
Select item 127145730.	NM_002875.5(RAD51):c.87+110A>G GRCh37: Chr15:40991153 GRCh38: Chr15:40698955	RAD51		not provided	Benign (Jun 23, 2018)	criteria provided, single submitter
Select item 131710231.	NM_002875.5(RAD51):c.87+290G>A GRCh37: Chr15:40991333 GRCh38: Chr15:40699135	RAD51		not provided	Likely benign (Apr 6, 2021)	criteria provided, single submitter
Select item 127466332.	NM_002875.5(RAD51):c.88-257del GRCh37: Chr15:40992998 GRCh38: Chr15:40700800	RAD51		not provided	Benign (Mar 31, 2019)	criteria provided, single submitter
Select item 176580633.	NM_002875.5(RAD51):c.90G>A (p.Gln30=) GRCh37: Chr15:40993264 GRCh38: Chr15:40701066	RAD51		Inborn genetic diseases	Likely benign (Oct 11, 2022)	criteria provided, single submitter
Select item 176718134.	NM_002875.5(RAD51):c.94G>T (p.Gly32Cys) GRCh37: Chr15:40993268 GRCh38: Chr15:40701070	RAD51	G32C	Inborn genetic diseases	Uncertain significance (Jun 4, 2022)	criteria provided, single submitter
Select item 177653735.	NM_002875.5(RAD51):c.104C>A (p.Ala35Asp) GRCh37: Chr15:40993278 GRCh38: Chr15:40701080	RAD51	A35D	Inborn genetic diseases	Uncertain significance (Jun 21, 2022)	criteria provided, single submitter
Select item 178883036.	NM_002875.5(RAD51):c.108C>T (p.Asn36=) GRCh37: Chr15:40993282 GRCh38: Chr15:40701084	RAD51		Inborn genetic diseases, not provided	Likely benign (Mar 1, 2023)	criteria provided, multiple submitters, no conflicts
Select item 249766737.	NM_002875.5(RAD51):c.109G>C (p.Asp37His) GRCh37: Chr15:40993283 GRCh38: Chr15:40701085	RAD51	D37H	Inborn genetic diseases	Uncertain significance (Dec 3, 2022)	criteria provided, single submitter
Select item 133698338.	NM_002875.5(RAD51):c.109G>A (p.Asp37Asn) GRCh37: Chr15:40993283 GRCh38: Chr15:40701085	RAD51	D37N	not specified	Uncertain significance (Jan 28, 2019)	criteria provided, single submitter
Select item 262469139.	NM_002875.5(RAD51):c.110A>T (p.Asp37Val) GRCh37: Chr15:40993284 GRCh38: Chr15:40701086	RAD51	D37V	Inborn genetic diseases	Uncertain significance (Aug 25, 2023)	criteria provided, single submitter
Select item 179745940.	NM_002875.5(RAD51):c.111T>C (p.Asp37=) GRCh37: Chr15:40993285 GRCh38: Chr15:40701087	RAD51		Inborn genetic diseases	Likely benign (Dec 23, 2021)	criteria provided, single submitter
Select item 175284141.	NM_002875.5(RAD51):c.121T>C (p.Leu41=) GRCh37: Chr15:40993295 GRCh38: Chr15:40701097	RAD51		Inborn genetic diseases	Likely benign (Oct 22, 2019)	criteria provided, single submitter
Select item 250204342.	NM_002875.5(RAD51):c.122T>G (p.Leu41Trp) GRCh37: Chr15:40993296 GRCh38: Chr15:40701098	RAD51	L41W	not provided	Uncertain significance (Nov 9, 2022)	criteria provided, single submitter
Select item 258595043.	NM_002875.5(RAD51):c.131C>G (p.Ala44Gly) GRCh37: Chr15:40993305 GRCh38: Chr15:40701107	RAD51	A44G	Inborn genetic diseases	Uncertain significance (Aug 30, 2023)	criteria provided, single submitter
Select item 246265044.	NM_002875.5(RAD51):c.131C>T (p.Ala44Val) GRCh37: Chr15:40993305 GRCh38: Chr15:40701107	RAD51	A44V	Inborn genetic diseases	Uncertain significance (Nov 19, 2022)	criteria provided, single submitter
Select item 177012245.	NM_002875.5(RAD51):c.132T>C (p.Ala44=) GRCh37: Chr15:40993306 GRCh38: Chr15:40701108	RAD51		Inborn genetic diseases	Likely benign (Jan 5, 2022)	criteria provided, single submitter
Select item 258594546.	NM_002875.5(RAD51):c.133G>A (p.Gly45Arg) GRCh37: Chr15:40993307 GRCh38: Chr15:40701109	RAD51	G45R	Inborn genetic diseases	Uncertain significance (Jun 25, 2023)	criteria provided, single submitter
Select item 177149847.	NM_002875.5(RAD51):c.138C>G (p.Phe46Leu) GRCh37: Chr15:40993312 GRCh38: Chr15:40701114	RAD51	F46L	Inborn genetic diseases	Uncertain significance (Jul 29, 2021)	criteria provided, single submitter
Select item 18780248.	NM_002875.5(RAD51):c.140A>G (p.His47Arg) GRCh37: Chr15:40993314 GRCh38: Chr15:40701116	RAD51	H47R	Mirror movements 2	not provided	no assertion provided
Select item 256548649.	NM_002875.5(RAD51):c.143C>A (p.Thr48Asn) GRCh37: Chr15:40993317 GRCh38: Chr15:40701119	RAD51	T48N	Inborn genetic diseases	Uncertain significance (May 21, 2023)	criteria provided, single submitter
Select item 74393750.	NM_002875.5(RAD51):c.144T>C (p.Thr48=) GRCh37: Chr15:40993318 GRCh38: Chr15:40701120	RAD51		Inborn genetic diseases, not provided	Likely benign (May 25, 2022)	criteria provided, multiple submitters, no conflicts
Select item 245085151.	NM_002875.5(RAD51):c.158C>G (p.Ala53Gly) GRCh37: Chr15:40993332 GRCh38: Chr15:40701134	RAD51	A53G	Inborn genetic diseases	Uncertain significance (Nov 24, 2022)	criteria provided, single submitter
Select item 177680552.	NM_002875.5(RAD51):c.162T>C (p.Tyr54=) GRCh37: Chr15:40993336 GRCh38: Chr15:40701138	RAD51		Inborn genetic diseases	Likely benign (Jul 19, 2022)	criteria provided, single submitter
Select item 73004753.	NM_002875.5(RAD51):c.164C>T (p.Ala55Val) GRCh37: Chr15:40993338 GRCh38: Chr15:40701140	RAD51	A55V	not specified, not provided	Benign/Likely benign (Dec 31, 2019)	criteria provided, multiple submitters, no conflicts
Select item 177746054.	NM_002875.5(RAD51):c.165G>T (p.Ala55=) GRCh37: Chr15:40993339 GRCh38: Chr15:40701141	RAD51		not provided, Inborn genetic diseases	Likely benign (Aug 8, 2022)	criteria provided, multiple submitters, no conflicts
Select item 177745355.	NM_002875.5(RAD51):c.165G>A (p.Ala55=) GRCh37: Chr15:40993339 GRCh38: Chr15:40701141	RAD51		Inborn genetic diseases	Likely benign (Jul 30, 2022)	criteria provided, single submitter
Select item 219256956.	NM_002875.5(RAD51):c.166C>T (p.Pro56Ser) GRCh37: Chr15:40993340 GRCh38: Chr15:40701142	RAD51	P56S	not provided	Benign (Jul 1, 2022)	criteria provided, single submitter
Select item 177787057.	NM_002875.5(RAD51):c.167C>T (p.Pro56Leu) GRCh37: Chr15:40993341 GRCh38: Chr15:40701143	RAD51	P56L	Inborn genetic diseases	Uncertain significance (Jul 31, 2021)	criteria provided, single submitter
Select item 178146758.	NM_002875.5(RAD51):c.185A>G (p.Asn62Ser) GRCh37: Chr15:40993359 GRCh38: Chr15:40701161	RAD51	N62S	Inborn genetic diseases	Uncertain significance (Feb 26, 2022)	criteria provided, single submitter
Select item 249766659.	NM_002875.5(RAD51):c.189T>G (p.Ile63Met) GRCh37: Chr15:40993363 GRCh38: Chr15:40701165	RAD51	I63M	Inborn genetic diseases	Uncertain significance (Jan 20, 2023)	criteria provided, single submitter
Select item 169555660.	NM_002875.5(RAD51):c.200G>A (p.Ser67Asn) GRCh37: Chr15:40993374 GRCh38: Chr15:40701176	RAD51	S67N	not provided	Uncertain significance (Jul 19, 2023)	criteria provided, single submitter
Select item 245086261.	NM_002875.5(RAD51):c.204A>C (p.Glu68Asp) GRCh37: Chr15:40993378 GRCh38: Chr15:40701180	RAD51	E68D	Inborn genetic diseases	Uncertain significance (Feb 25, 2023)	criteria provided, single submitter
Select item 262469562.	NM_002875.5(RAD51):c.205G>A (p.Ala69Thr) GRCh37: Chr15:40993379 GRCh38: Chr15:40701181	RAD51	A69T	Inborn genetic diseases	Uncertain significance (Aug 1, 2023)	criteria provided, single submitter
Select item 178520663.	NM_002875.5(RAD51):c.205G>C (p.Ala69Pro) GRCh37: Chr15:40993379 GRCh38: Chr15:40701181	RAD51	A69P	Inborn genetic diseases	Uncertain significance (Mar 14, 2022)	criteria provided, single submitter
Select item 246272064.	NM_002875.5(RAD51):c.210A>G (p.Lys70=) GRCh37: Chr15:40993384 GRCh38: Chr15:40701186	RAD51		Inborn genetic diseases	Likely benign (Jan 22, 2023)	criteria provided, single submitter
Select item 178672965.	NM_002875.5(RAD51):c.214G>T (p.Asp72Tyr) GRCh37: Chr15:40993388 GRCh38: Chr15:40701190	RAD51	D72Y	Inborn genetic diseases	Uncertain significance (Apr 2, 2022)	criteria provided, single submitter
Select item 121176966.	NM_002875.5(RAD51):c.225+190dup GRCh37: Chr15:40993574-40993575 GRCh38: Chr15:40701376-40701377	RAD51		not provided	Likely benign (Oct 29, 2019)	criteria provided, single submitter
Select item 122727667.	NM_002875.5(RAD51):c.225+190del GRCh37: Chr15:40993575 GRCh38: Chr15:40701377	RAD51		not provided	Benign (Sep 22, 2019)	criteria provided, single submitter
Select item 126353168.	NM_002875.5(RAD51):c.225+311C>T GRCh37: Chr15:40993710 GRCh38: Chr15:40701512	RAD51		not provided	Benign (Jan 10, 2019)	criteria provided, single submitter
Select item 121254669.	NM_002875.5(RAD51):c.225+314C>T GRCh37: Chr15:40993713 GRCh38: Chr15:40701515	RAD51		not provided	Likely benign (Jan 10, 2019)	criteria provided, single submitter
Select item 119600870.	NM_002875.5(RAD51):c.225+426G>T GRCh37: Chr15:40993825 GRCh38: Chr15:40701627	RAD51		not provided	Likely benign (Dec 10, 2020)	criteria provided, single submitter
Select item 119770271.	NM_002875.5(RAD51):c.225+600_225+601del GRCh37: Chr15:40993975-40993976 GRCh38: Chr15:40701777-40701778	RAD51		not provided	Likely benign (Aug 13, 2019)	criteria provided, single submitter
Select item 264518272.	NM_002875.5(RAD51):c.225+607G>A GRCh37: Chr15:40994006 GRCh38: Chr15:40701808	RAD51		not provided	Benign (Oct 1, 2023)	criteria provided, single submitter
Select item 105007173.	NM_002875.5(RAD51):c.225+615G>A GRCh37: Chr15:40994014 GRCh38: Chr15:40701816	RAD51	R79H	not provided	Uncertain significance	no assertion criteria provided
Select item 264518374.	NM_002875.5(RAD51):c.225+668C>T GRCh37: Chr15:40994067 GRCh38: Chr15:40701869	RAD51	R97C	not provided	Benign (Oct 1, 2022)	criteria provided, single submitter
Select item 264518475.	NM_002875.5(RAD51):c.225+685T>C GRCh37: Chr15:40994084 GRCh38: Chr15:40701886	RAD51		not provided	Likely benign (Oct 1, 2022)	criteria provided, single submitter
Select item 244528176.	NM_002875.5(RAD51):c.225+719A>C GRCh37: Chr15:40994118 GRCh38: Chr15:40701920	RAD51	T114P	Ovarian cancer	Benign (Jan 1, 2022)	criteria provided, single submitter
Select item 129457477.	NM_002875.5(RAD51):c.225+893_225+896del GRCh37: Chr15:40994285-40994288 GRCh38: Chr15:40702087-40702090	RAD51		not provided	Benign (Mar 30, 2021)	criteria provided, single submitter
Select item 123187178.	NM_002875.5(RAD51):c.226-72del GRCh37: Chr15:40998303 GRCh38: Chr15:40706105	RAD51		not provided	Benign (Jun 23, 2018)	criteria provided, single submitter
Select item 123084879.	NM_002875.5(RAD51):c.226-70T>A GRCh37: Chr15:40998305 GRCh38: Chr15:40706107	RAD51		not provided	Benign (Jun 22, 2018)	criteria provided, single submitter
Select item 125525780.	NM_002875.5(RAD51):c.226-33T>G GRCh37: Chr15:40998342 GRCh38: Chr15:40706144	RAD51		not provided	Benign (Jun 23, 2018)	criteria provided, single submitter
Select item 178890881.	NM_002875.5(RAD51):c.227C>G (p.Ala76Gly) GRCh37: Chr15:40998376 GRCh38: Chr15:40706178	RAD51	A76G	Inborn genetic diseases	Uncertain significance (Dec 25, 2021)	criteria provided, single submitter
Select item 262469482.	NM_002875.5(RAD51):c.230A>G (p.Glu77Gly) GRCh37: Chr15:40998379 GRCh38: Chr15:40706181	RAD51	E77G	Inborn genetic diseases	Uncertain significance (Jul 12, 2023)	criteria provided, single submitter
Select item 178983583.	NM_002875.5(RAD51):c.233C>T (p.Ala78Val) GRCh37: Chr15:40998382 GRCh38: Chr15:40706184	RAD51	A78V	Inborn genetic diseases	Uncertain significance (Feb 3, 2022)	criteria provided, single submitter
Select item 212984784.	NM_002875.5(RAD51):c.236C>T (p.Ala79Val) GRCh37: Chr15:40998385 GRCh38: Chr15:40706187	RAD51	A79V	not provided	Uncertain significance (May 17, 2022)	criteria provided, single submitter
Select item 259270885.	NM_002875.5(RAD51):c.238A>G (p.Lys80Glu) GRCh37: Chr15:40998387 GRCh38: Chr15:40706189	RAD51	K80E	Inborn genetic diseases	Uncertain significance (Jul 9, 2023)	criteria provided, single submitter
Select item 258594686.	NM_002875.5(RAD51):c.239A>C (p.Lys80Thr) GRCh37: Chr15:40998388 GRCh38: Chr15:40706190	RAD51	K80T	Inborn genetic diseases	Uncertain significance (Jun 28, 2023)	criteria provided, single submitter
Select item 179115687.	NM_002875.5(RAD51):c.242T>C (p.Leu81Ser) GRCh37: Chr15:40998391 GRCh38: Chr15:40706193	RAD51	L81S	Inborn genetic diseases	Uncertain significance (Feb 27, 2022)	criteria provided, single submitter
Select item 179146688.	NM_002875.5(RAD51):c.244G>A (p.Val82Ile) GRCh37: Chr15:40998393 GRCh38: Chr15:40706195	RAD51	V82I	Inborn genetic diseases	Uncertain significance (Jul 14, 2021)	criteria provided, single submitter
Select item 179204489.	NM_002875.5(RAD51):c.248C>G (p.Pro83Arg) GRCh37: Chr15:40998397 GRCh38: Chr15:40706199	RAD51	P83R	Inborn genetic diseases	Uncertain significance (Feb 1, 2022)	criteria provided, single submitter
Select item 245085490.	NM_002875.5(RAD51):c.249A>T (p.Pro83=) GRCh37: Chr15:40998398 GRCh38: Chr15:40706200	RAD51		Inborn genetic diseases	Likely benign (Jan 27, 2023)	criteria provided, single submitter
Select item 179235991.	NM_002875.5(RAD51):c.250A>G (p.Met84Val) GRCh37: Chr15:40998399 GRCh38: Chr15:40706201	RAD51	M84V	Inborn genetic diseases, not provided	Uncertain significance (Jul 15, 2022)	criteria provided, multiple submitters, no conflicts
Select item 179349092.	NM_002875.5(RAD51):c.258C>T (p.Phe86=) GRCh37: Chr15:40998407 GRCh38: Chr15:40706209	RAD51		not provided, Inborn genetic diseases	Likely benign (Jul 5, 2022)	criteria provided, multiple submitters, no conflicts
Select item 179391493.	NM_002875.5(RAD51):c.261C>T (p.Thr87=) GRCh37: Chr15:40998410 GRCh38: Chr15:40706212	RAD51		Inborn genetic diseases	Likely benign (Feb 21, 2022)	criteria provided, single submitter
Select item 245085294.	NM_002875.5(RAD51):c.263C>T (p.Thr88Ile) GRCh37: Chr15:40998412 GRCh38: Chr15:40706214	RAD51	T88I	Inborn genetic diseases	Uncertain significance (Dec 12, 2022)	criteria provided, single submitter
Select item 179416795.	NM_002875.5(RAD51):c.263C>G (p.Thr88Ser) GRCh37: Chr15:40998412 GRCh38: Chr15:40706214	RAD51	T88S	Inborn genetic diseases	Uncertain significance (Apr 21, 2022)	criteria provided, single submitter
Select item 179432396.	NM_002875.5(RAD51):c.264T>C (p.Thr88=) GRCh37: Chr15:40998413 GRCh38: Chr15:40706215	RAD51		Inborn genetic diseases	Likely benign (Aug 3, 2022)	criteria provided, single submitter
Select item 179477197.	NM_002875.5(RAD51):c.268A>G (p.Thr90Ala) GRCh37: Chr15:40998417 GRCh38: Chr15:40706219	RAD51	T90A	Inborn genetic diseases	Uncertain significance (Oct 22, 2022)	criteria provided, single submitter
Select item 210382798.	NM_002875.5(RAD51):c.269C>G (p.Thr90Ser) GRCh37: Chr15:40998418 GRCh38: Chr15:40706220	RAD51	T90S	Inborn genetic diseases, not provided	Uncertain significance (Sep 10, 2023)	criteria provided, multiple submitters, no conflicts
Select item 245086499.	NM_002875.5(RAD51):c.275T>C (p.Phe92Ser) GRCh37: Chr15:40998424 GRCh38: Chr15:40706226	RAD51	F92S	Inborn genetic diseases	Uncertain significance (Mar 5, 2023)	criteria provided, single submitter
Select item 1796132100.	NM_002875.5(RAD51):c.279C>T (p.His93=) GRCh37: Chr15:40998428 GRCh38: Chr15:40706230	RAD51		Inborn genetic diseases	Likely benign (Aug 13, 2021)	criteria provided, single submitter

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