ClinVar for Gene (Select 6098) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3155782	NM_001378902.1(ROS1):c.976C>T (p.Arg326Trp)	ROS1 (R326W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155780	NM_001378902.1(ROS1):c.6729T>G (p.Asp2243Glu)	ROS1 (D2245E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155779	NM_001378902.1(ROS1):c.6718G>A (p.Glu2240Lys)	ROS1 (E2240K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155778	NM_001378902.1(ROS1):c.6470C>G (p.Pro2157Arg)	ROS1 (P2157R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155777	NM_001378902.1(ROS1):c.6298G>T (p.Ala2100Ser)	ROS1 (A2106S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155776	NM_001378902.1(ROS1):c.6081C>A (p.Asp2027Glu)	ROS1 (D2027E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155774	NM_001378902.1(ROS1):c.5999A>G (p.His2000Arg)	ROS1 (H2002R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155773	NM_001378902.1(ROS1):c.5789A>G (p.Asn1930Ser)	ROS1 (N1930S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3155771	NM_001378902.1(ROS1):c.5225C>A (p.Thr1742Lys)	ROS1 (T1742K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155770	NM_001378902.1(ROS1):c.5209C>G (p.Pro1737Ala)	ROS1 (P1739A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155769	NM_001378902.1(ROS1):c.5105A>T (p.Gln1702Leu)	ROS1 (Q1702L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155768	NM_001378902.1(ROS1):c.5083C>G (p.His1695Asp)	ROS1 (H1695D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155766	NM_001378902.1(ROS1):c.4931C>T (p.Pro1644Leu)	ROS1 (P1646L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155765	NM_001378902.1(ROS1):c.4646A>C (p.Asn1549Thr)	ROS1 (N1551T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155764	NM_001378902.1(ROS1):c.485A>G (p.Tyr162Cys)	ROS1 (Y162C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155763	NM_001378902.1(ROS1):c.4553C>T (p.Ser1518Leu)	ROS1 (S1518L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155762	NM_001378902.1(ROS1):c.4547C>A (p.Pro1516Gln)	ROS1 (P1518Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155760	NM_001378902.1(ROS1):c.4358C>T (p.Ala1453Val)	ROS1 (A1453V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155759	NM_001378902.1(ROS1):c.4304A>G (p.Asp1435Gly)	ROS1 (D1437G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155758	NM_001378902.1(ROS1):c.4154A>T (p.Asp1385Val)	ROS1 (D1385V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155757	NM_001378902.1(ROS1):c.3882G>A (p.Met1294Ile)	ROS1 (M1295I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155756	NM_001378902.1(ROS1):c.391G>A (p.Ala131Thr)	ROS1 (A131T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155755	NM_001378902.1(ROS1):c.3268A>T (p.Asn1090Tyr)	ROS1 (N1091Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155754	NM_001378902.1(ROS1):c.3260G>A (p.Ser1087Asn)	ROS1 (S1087N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155753	NM_001378902.1(ROS1):c.2804T>C (p.Phe935Ser)	ROS1 (F936S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155752	NM_001378902.1(ROS1):c.2777C>T (p.Thr926Ile)	ROS1 (T926I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155751	NM_001378902.1(ROS1):c.26C>T (p.Pro9Leu)	ROS1 (P9L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3155750	NM_001378902.1(ROS1):c.2579A>G (p.Gln860Arg)	ROS1 (Q865R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155749	NM_001378902.1(ROS1):c.2522A>G (p.Tyr841Cys)	ROS1 (Y841C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155748	NM_001378902.1(ROS1):c.2419A>G (p.Thr807Ala)	ROS1 (T807A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155747	NM_001378902.1(ROS1):c.2312C>T (p.Thr771Met)	ROS1 (T771M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155746	NM_001378902.1(ROS1):c.2053C>A (p.Pro685Thr)	ROS1 (P685T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155745	NM_001378902.1(ROS1):c.1736C>T (p.Ser579Phe)	ROS1 (S579F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155744	NM_001378902.1(ROS1):c.1723G>A (p.Val575Met)	ROS1 (V575M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155743	NM_001378902.1(ROS1):c.1352G>A (p.Arg451Gln)	ROS1 (R451Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3062896	GRCh37/hg19 6q21-23.2(chr6:110546061-131896074)x3	AKAP7, AMD1 +87 more	Copy number gain	not specified	GLikely pathogenic
Select item 3043741	NM_001378902.1(ROS1):c.6967C>G (p.Pro2323Ala)	ROS1 (P2323A +2 more)	Single nucleotide variant (missense variant)	ROS1-related disorder	GLikely benign
Select item 3040207	NM_001378902.1(ROS1):c.2796A>C (p.Pro932=)	ROS1	Single nucleotide variant (synonymous variant)	ROS1-related disorder	GLikely benign
Select item 3034098	NM_001378902.1(ROS1):c.1135T>C (p.Ser379Pro)	ROS1 (S370P +1 more)	Single nucleotide variant (missense variant)	ROS1-related disorder	GLikely benign
Select item 3032799	NM_001378902.1(ROS1):c.1181T>C (p.Met394Thr)	ROS1 (M385T +1 more)	Single nucleotide variant (missense variant)	ROS1-related disorder	GLikely benign
Select item 2690966	NM_001378902.1(ROS1):c.3611T>A (p.Leu1204Ter)	ROS1 (L1204* +2 more)	Single nucleotide variant (nonsense)	Male infertility with azoospermia or oligozoospermia due to single gene mutation	GLikely pathogenic
Select item 2690965	NM_001378902.1(ROS1):c.5588dup (p.Ile1864fs)	ROS1 (I1864fs +2 more)	Duplication (frameshift variant)	Male infertility with azoospermia or oligozoospermia due to single gene mutation	GLikely pathogenic
Select item 2673077	NM_001378902.1(ROS1):c.6621C>A (p.Asp2207Glu)	ROS1 (D2207E +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2656873	NM_001378902.1(ROS1):c.2962T>G (p.Leu988Val)	ROS1 (L988V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2656872	NM_001378902.1(ROS1):c.3543C>T (p.Ala1181=)	ROS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656871	NM_001378902.1(ROS1):c.5623+1427_5623+1429dup	ROS1	Duplication (intron variant)	not provided	GBenign
Select item 2656870	NM_001378902.1(ROS1):c.5760-265G>T	ROS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2656869	NM_001378902.1(ROS1):c.6369T>C (p.Ala2123=)	ROS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2623106	NM_001378902.1(ROS1):c.2929T>C (p.Tyr977His)	ROS1 (Y977H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620000	NM_001378902.1(ROS1):c.884T>C (p.Val295Ala)	ROS1 (V286A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619142	NM_001378902.1(ROS1):c.3298A>C (p.Asn1100His)	ROS1 (N1101H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616628	NM_001378902.1(ROS1):c.3616A>G (p.Asn1206Asp)	ROS1 (N1206D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611123	NM_001378902.1(ROS1):c.1019A>T (p.Asp340Val)	ROS1 (D331V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606631	NM_001378902.1(ROS1):c.5290C>G (p.Gln1764Glu)	ROS1 (Q1764E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599544	NM_001378902.1(ROS1):c.1717C>G (p.Leu573Val)	ROS1 (L564V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599470	NM_001378902.1(ROS1):c.3746T>C (p.Val1249Ala)	ROS1 (V1250A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599207	NM_001378902.1(ROS1):c.6142G>A (p.Val2048Ile)	ROS1 (V2048I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597791	NM_001378902.1(ROS1):c.2711T>C (p.Ile904Thr)	ROS1 (I909T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2579265	GRCh38/hg38 6q21-23.1(chr6:113857248-130442177)x1	ARHGAP18, ASF1A +316 more	Copy number loss	Intellectual disability, autosomal dominant 55, with seizures	GPathogenic
Select item 2574685	GRCh37/hg19 6q21-22.31(chr6:112713854-124105184)	ASF1A, CALHM4 +39 more	Copy number loss	6q terminal deletion syndrome	GLikely pathogenic
Select item 2559454	NM_001378902.1(ROS1):c.1676C>T (p.Ser559Leu)	ROS1 (S550L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559381	NM_001378902.1(ROS1):c.5073T>A (p.Asn1691Lys)	ROS1 (N1693K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552842	NM_001378902.1(ROS1):c.3531A>T (p.Arg1177Ser)	ROS1 (R1182S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551624	NM_001378902.1(ROS1):c.139C>T (p.Leu47Phe)	ROS1 (L47F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549537	NM_001378902.1(ROS1):c.5165G>A (p.Arg1722Lys)	ROS1 (R1724K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547690	NM_001378902.1(ROS1):c.3928C>A (p.Pro1310Thr)	ROS1 (P1311T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543434	NM_001378902.1(ROS1):c.6236G>A (p.Cys2079Tyr)	ROS1 (C2085Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532626	NM_001378902.1(ROS1):c.1132A>G (p.Ile378Val)	ROS1 (I378V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527531	NM_001378902.1(ROS1):c.3248T>C (p.Ile1083Thr)	ROS1 (I1083T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521553	NM_001378902.1(ROS1):c.5949G>T (p.Gln1983His)	ROS1 (Q1989H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520402	NM_001378902.1(ROS1):c.6752A>G (p.Asp2251Gly)	ROS1 (D2251G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510511	NM_001378902.1(ROS1):c.5326A>C (p.Thr1776Pro)	ROS1 (T1778P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492521	NM_001378902.1(ROS1):c.4193G>T (p.Ser1398Ile)	ROS1 (S1398I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490979	NM_001378902.1(ROS1):c.5030A>G (p.Asn1677Ser)	ROS1 (N1683S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455419	NM_001378902.1(ROS1):c.2665C>T (p.Arg889Trp)	ROS1 (R889W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2443073	NM_001378902.1(ROS1):c.6079G>A (p.Asp2027Asn)	ROS1 (D2027N +2 more)	Single nucleotide variant (missense variant)	Lung sarcomatoid carcinoma	GUncertain significance
Select item 2431185	NM_001378902.1(ROS1):c.3366+23T>C	ROS1	Single nucleotide variant (intron variant)	Squamous cell carcinoma	GUncertain significance
Select item 2431181	NM_001378902.1(ROS1):c.3167A>G (p.Asn1056Ser)	ROS1 (N1056S +2 more)	Single nucleotide variant (missense variant)	Lung adenocarcinoma	GUncertain significance
Select item 2431152	NM_001378902.1(ROS1):c.682C>G (p.Gln228Glu)	ROS1 (Q219E +1 more)	Single nucleotide variant (missense variant)	Lung adenocarcinoma	GUncertain significance
Select item 2431128	NM_001378902.1(ROS1):c.5062-46A>C	ROS1	Single nucleotide variant (intron variant)	Lung adenocarcinoma	GUncertain significance
Select item 2431087	NM_001378902.1(ROS1):c.3388G>A (p.Gly1130Arg)	ROS1 (G1130R +2 more)	Single nucleotide variant (missense variant)	Lung adenocarcinoma	GPathogenic
Select item 2431067	NM_001378902.1(ROS1):c.3430+42C>T	ROS1	Single nucleotide variant (intron variant)	Lung adenocarcinoma	GBenign
Select item 2427242	NC_000006.11:g.(?_116441236)_(119252888_?)del	TRAPPC3L, TSPYL4 +24 more	Deletion	Congenital disorder of glycosylation, type IAA	GPathogenic
Select item 2410056	NM_001378902.1(ROS1):c.3163A>G (p.Lys1055Glu)	ROS1 (K1060E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409172	NM_001378902.1(ROS1):c.3544G>A (p.Val1182Ile)	ROS1 (V1182I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2407943	NM_001378902.1(ROS1):c.6641A>T (p.Asn2214Ile)	ROS1 (N2214I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403585	NM_001378902.1(ROS1):c.5893G>A (p.Gly1965Arg)	ROS1 (G1967R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400022	NM_001378902.1(ROS1):c.2674T>C (p.Trp892Arg)	ROS1 (W892R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394971	NM_001378902.1(ROS1):c.2375T>C (p.Val792Ala)	ROS1 (V792A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390651	NM_001378902.1(ROS1):c.6942A>C (p.Gln2314His)	ROS1 (Q2314H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386720	NM_001378902.1(ROS1):c.6934G>A (p.Glu2312Lys)	ROS1 (E2312K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370018	NM_001378902.1(ROS1):c.2573G>A (p.Arg858Gln)	ROS1 (R863Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363916	NM_001378902.1(ROS1):c.267T>G (p.Cys89Trp)	ROS1 (C80W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355768	NM_001378902.1(ROS1):c.994C>A (p.His332Asn)	ROS1 (H332N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355129	NM_001378902.1(ROS1):c.3145A>G (p.Ser1049Gly)	ROS1 (S1050G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354957	NM_001378902.1(ROS1):c.3841C>T (p.Arg1281Cys)	ROS1 (R1281C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354045	NM_001378902.1(ROS1):c.895G>C (p.Glu299Gln)	ROS1 (E290Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351398	NM_001378902.1(ROS1):c.5197A>C (p.Ser1733Arg)	ROS1 (S1735R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342880	NM_001378902.1(ROS1):c.2176C>A (p.Leu726Met)	ROS1 (L731M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342096	NM_001378902.1(ROS1):c.1460T>C (p.Met487Thr)	ROS1 (M478T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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