ClinVar for MedGen (Select 373234) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2681776	NM_024426.6(WT1):c.1384C>T (p.Gln462Ter)	WT1 (Q208* +11 more)	Single nucleotide variant (nonsense +2 more)	Meacham syndrome +3 more	GLikely pathogenic
Select item 1809679	NM_024426.6(WT1):c.163G>A (p.Ala55Thr)	LOC107982234, WT1 (A50T +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +7 more	GUncertain significance
Select item 1667997	NM_024426.6(WT1):c.887+14G>A	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +7 more	GBenign/Likely benign
Select item 1588499	NM_024426.6(WT1):c.1264+19C>T	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +7 more	GLikely benign
Select item 1576116	NM_024426.6(WT1):c.1016+15C>T	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +7 more	GLikely benign
Select item 1540733	NM_024426.6(WT1):c.780G>A (p.Ser260=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Wilms tumor 1 +7 more	GLikely benign
Select item 1495132	NM_024426.6(WT1):c.661+15G>T	LOC107982234, WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +7 more	GConflicting classifications of pathogenicity
Select item 1470255	NM_024426.6(WT1):c.785-14G>A	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +7 more	GUncertain significance
Select item 1426680	NM_024426.6(WT1):c.887+19C>G	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +7 more	GConflicting classifications of pathogenicity
Select item 1409524	NM_024426.6(WT1):c.459C>T (p.Gly153=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +7 more	GConflicting classifications of pathogenicity
Select item 1038185	NM_024426.6(WT1):c.1127T>C (p.Val376Ala)	WT1 (V359A +9 more)	Single nucleotide variant (missense variant +2 more)	11p partial monosomy syndrome +7 more	GUncertain significance
Select item 1017207	NM_024426.6(WT1):c.989C>T (p.Ser330Leu)	WT1 (S113L +4 more)	Single nucleotide variant (missense variant +2 more)	Aniridia 1 +7 more	GUncertain significance
Select item 971511	NM_024426.6(WT1):c.1162T>C (p.Ser388Pro)	WT1 (S171P +9 more)	Single nucleotide variant (missense variant +2 more)	Frasier syndrome +7 more	GUncertain significance
Select item 966883	NM_024426.6(WT1):c.722C>T (p.Ala241Val)	WT1 (A241V +2 more)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +7 more	GUncertain significance
Select item 961780	NM_024426.6(WT1):c.653G>A (p.Arg218His)	LOC107982234, WT1 (R218H)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +7 more	GUncertain significance
Select item 954239	NM_024426.6(WT1):c.351C>T (p.Gly117=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +7 more	GUncertain significance
Select item 943533	NM_024426.6(WT1):c.1253G>T (p.Arg418Met)	WT1 (R184M +10 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +7 more	GUncertain significance
Select item 939929	NM_024426.6(WT1):c.1559T>C (p.Leu520Pro)	WT1 (L517P +14 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +8 more	GUncertain significance
Select item 935383	NM_024426.6(WT1):c.646G>A (p.Ala216Thr)	LOC107982234, WT1 (A216T)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +8 more	GUncertain significance
Select item 879620	NM_024426.6(WT1):c.813G>C (p.Pro271=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Frasier syndrome +6 more	GConflicting classifications of pathogenicity
Select item 879521	NM_024426.6(WT1):c.*100A>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Meacham syndrome +2 more	GUncertain significance
Select item 879412	NM_024426.6(WT1):c.*1066T>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Meacham syndrome +2 more	GUncertain significance
Select item 878161	NM_024426.6(WT1):c.973G>A (p.Ala325Thr)	WT1 (A108T +4 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +5 more	GUncertain significance
Select item 878010	NM_024426.6(WT1):c.*629T>C	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 877955	NM_024426.6(WT1):c.*5T>C	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +3 more	GConflicting classifications of pathogenicity
Select item 877954	NM_024426.6(WT1):c.*12C>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Wilms tumor 1 +2 more	GConflicting classifications of pathogenicity
Select item 877311	NM_024426.6(WT1):c.-87C>T	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 877249	NM_024426.6(WT1):c.298C>G (p.Pro100Ala)	LOC107982234, WT1 (P100A)	Single nucleotide variant (missense variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 877125	NM_024426.6(WT1):c.1020C>T (p.His340=)	WT1	Single nucleotide variant (synonymous variant +3 more)	Frasier syndrome +5 more	GConflicting classifications of pathogenicity
Select item 864517	NM_024426.6(WT1):c.26C>T (p.Pro9Leu)	LOC107982234, WT1 (P9L)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +8 more	GUncertain significance
Select item 861660	NM_024426.6(WT1):c.628T>G (p.Cys210Gly)	LOC107982234, WT1 (C210G)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +7 more	GUncertain significance
Select item 842948	NM_024426.6(WT1):c.620T>G (p.Leu207Arg)	LOC107982234, WT1 (L207R)	Single nucleotide variant (missense variant +1 more)	Nephrotic syndrome, type 4 +6 more	GUncertain significance
Select item 840419	NM_024426.6(WT1):c.313G>T (p.Ala105Ser)	LOC107982234, WT1 (A105S)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +5 more	GUncertain significance
Select item 721377	NM_024426.6(WT1):c.402G>A (p.Pro134=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +6 more	GConflicting classifications of pathogenicity
Select item 706001	NM_024426.6(WT1):c.115C>A (p.Arg39=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Aniridia 1 +8 more	GLikely benign
Select item 695998	NM_024426.6(WT1):c.27G>A (p.Pro9=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not provided +10 more	GLikely benign
Select item 666088	NM_024426.6(WT1):c.1562C>T (p.Ala521Val)	WT1 (A125V +14 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +8 more	GUncertain significance
Select item 665246	NM_024426.6(WT1):c.591G>T (p.Gln197His)	LOC107982234, WT1 (Q197H)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +7 more	GUncertain significance
Select item 663192	NM_024426.6(WT1):c.223G>A (p.Gly75Ser)	LOC107982234, WT1 (G75S)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +7 more	GUncertain significance
Select item 659841	NM_024426.6(WT1):c.1150G>A (p.Val384Ile)	WT1 (V167I +9 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +7 more	GUncertain significance
Select item 655847	NM_024426.6(WT1):c.1487A>G (p.Lys496Arg)	WT1 (K476R +14 more)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +7 more	GUncertain significance
Select item 654381	NM_024426.6(WT1):c.658C>A (p.Gln220Lys)	LOC107982234, WT1 (Q220K)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +8 more	GUncertain significance
Select item 639084	NM_024426.6(WT1):c.386C>A (p.Pro129Gln)	LOC107982234, WT1 (P129Q)	Single nucleotide variant (missense variant +1 more)	Aniridia 1 +7 more	GUncertain significance
Select item 599100	NM_024426.6(WT1):c.1388G>A (p.Arg463Gln)	WT1 (R246Q +10 more)	Single nucleotide variant (missense variant +1 more)	Nephrotic syndrome, type 4 +8 more	GConflicting classifications of pathogenicity
Select item 578155	NM_024426.6(WT1):c.386C>T (p.Pro129Leu)	LOC107982234, WT1 (P129L)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +7 more	GUncertain significance
Select item 566230	NM_024426.6(WT1):c.685G>A (p.Gly229Arg)	WT1 (G12R +1 more)	Single nucleotide variant (missense variant +1 more)	Meacham syndrome +8 more	GUncertain significance
Select item 543160	NM_024426.6(WT1):c.708G>A (p.Thr236=)	WT1	Single nucleotide variant (synonymous variant +3 more)	Meacham syndrome +7 more	GLikely benign
Select item 543156	NM_024426.6(WT1):c.1038C>T (p.Ser346=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Meacham syndrome +7 more	GLikely benign
Select item 543147	NM_024426.6(WT1):c.662-10G>T	WT1	Single nucleotide variant (intron variant)	Meacham syndrome +7 more	GLikely benign
Select item 543138	NM_024426.6(WT1):c.1142C>T (p.Pro381Leu)	WT1 (P164L +8 more)	Single nucleotide variant (missense variant +2 more)	Meacham syndrome +7 more	GUncertain significance
Select item 543136	NM_024426.6(WT1):c.1218A>C (p.Arg406Ser)	WT1 (R189S +9 more)	Single nucleotide variant (missense variant +1 more)	Meacham syndrome +7 more	GUncertain significance
Select item 543134	NM_024426.6(WT1):c.1158G>A (p.Ser386=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Meacham syndrome +7 more	GConflicting classifications of pathogenicity
Select item 543129	NM_024426.6(WT1):c.124G>A (p.Gly42Ser)	LOC107982234, WT1 (G42S)	Single nucleotide variant (missense variant +1 more)	Nephrotic syndrome, type 4 +6 more	GConflicting classifications of pathogenicity
Select item 543124	NM_024426.6(WT1):c.779C>T (p.Ser260Leu)	WT1 (S43L +2 more)	Single nucleotide variant (missense variant +1 more)	Meacham syndrome +7 more	GUncertain significance
Select item 543119	NM_024426.6(WT1):c.28_29delinsTA (p.Ala10Tyr)	LOC107982234, WT1 (A10Y)	Indel (missense variant +1 more)	Hereditary cancer-predisposing syndrome +9 more	GUncertain significance
Select item 543118	NM_024426.6(WT1):c.203G>A (p.Gly68Glu)	LOC107982234, WT1 (G68E)	Single nucleotide variant (missense variant +1 more)	not provided +8 more	GUncertain significance
Select item 515922	NM_024426.6(WT1):c.1568G>A (p.Ter523=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Kidney disorder +8 more	GConflicting classifications of pathogenicity
Select item 476718	NM_024426.6(WT1):c.746T>G (p.Phe249Cys)	WT1 (F32C +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +7 more	GUncertain significance
Select item 476699	NM_024426.6(WT1):c.314C>G (p.Ala105Gly)	LOC107982234, WT1 (A105G)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +8 more	GConflicting classifications of pathogenicity
Select item 476696	NM_024426.6(WT1):c.218A>T (p.Gln73Leu)	LOC107982234, WT1 (Q73L)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +10 more	GUncertain significance
Select item 476680	NM_024426.6(WT1):c.1161A>G (p.Ala387=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Wilms tumor 1 +8 more	GBenign/Likely benign
Select item 419332	NM_024426.6(WT1):c.1400G>A (p.Arg467Gln)	WT1 (R250Q +10 more)	Single nucleotide variant (missense variant +1 more)	Kidney disorder +11 more	GPathogenic/Likely pathogenic
Select item 414082	NM_024426.6(WT1):c.849C>T (p.Thr283=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Meacham syndrome +7 more	GLikely benign
Select item 414080	NM_024426.6(WT1):c.1182C>T (p.Arg394=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Drash syndrome +7 more	GConflicting classifications of pathogenicity
Select item 414075	NM_024426.6(WT1):c.1017-9T>C	WT1	Single nucleotide variant (intron variant)	Nephrotic syndrome, type 4 +5 more	GConflicting classifications of pathogenicity
Select item 414073	NM_024426.6(WT1):c.1448-10G>A	WT1	Single nucleotide variant (intron variant)	Meacham syndrome +8 more	GBenign/Likely benign
Select item 406695	NM_024426.6(WT1):c.439C>G (p.Gln147Glu)	LOC107982234, WT1 (Q147E)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +8 more	GUncertain significance
Select item 406692	NM_024426.6(WT1):c.1124G>A (p.Arg375His)	WT1 (R158H +8 more)	Single nucleotide variant (missense variant +2 more)	Nephrotic syndrome, type 4 +5 more	GConflicting classifications of pathogenicity
Select item 406688	NM_024426.6(WT1):c.785G>A (p.Gly262Asp)	WT1 (G45D +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 406685	NM_024426.6(WT1):c.600G>A (p.Met200Ile)	LOC107982234, WT1 (M200I)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +7 more	GUncertain significance
Select item 392045	NM_024426.6(WT1):c.691C>T (p.Pro231Ser)	WT1 (P14S +1 more)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +8 more	GUncertain significance
Select item 304442	NM_024426.6(WT1):c.-140C>T	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 304441	NM_024426.6(WT1):c.-135G>A	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Meacham syndrome +2 more	GUncertain significance
Select item 304440	NM_024426.6(WT1):c.-114T>A	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 304439	NM_024426.6(WT1):c.-110C>T	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 304438	NM_024426.6(WT1):c.-106C>T	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +4 more	GConflicting classifications of pathogenicity
Select item 304437	NM_024426.6(WT1):c.-102C>A	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +2 more	GUncertain significance
Select item 304436	NM_024426.6(WT1):c.-94G>C	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304435	NM_024426.6(WT1):c.-90T>C	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +3 more	GUncertain significance
Select item 304434	NM_024426.6(WT1):c.-86T>C	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304433	NM_024426.6(WT1):c.-82A>C	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304432	NM_024426.6(WT1):c.-76T>C	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	Wilms tumor 1 +2 more	GUncertain significance
Select item 304431	NM_024426.6(WT1):c.-31G>T	LOC107982234, WT1	Single nucleotide variant (5 prime UTR variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304430	NM_024426.6(WT1):c.136G>T (p.Ala46Ser)	LOC107982234, WT1 (A46S)	Single nucleotide variant (missense variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304429	NM_024426.6(WT1):c.162C>G (p.Ser54Arg)	LOC107982234, WT1 (S54R)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +6 more	GUncertain significance
Select item 304428	NM_024426.6(WT1):c.174C>G (p.Leu58=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 304427	NM_024426.6(WT1):c.247G>T (p.Ala83Ser)	LOC107982234, WT1 (A83S)	Single nucleotide variant (missense variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304426	NM_024426.6(WT1):c.285C>T (p.Gly95=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	11p partial monosomy syndrome +3 more	GUncertain significance
Select item 304425	NM_024426.6(WT1):c.347C>T (p.Pro116Leu)	LOC107982234, WT1 (P116L)	Single nucleotide variant (missense variant +1 more)	Meacham syndrome +6 more	GUncertain significance
Select item 304424	NM_024426.6(WT1):c.390A>G (p.Pro130=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +5 more	GConflicting classifications of pathogenicity
Select item 304423	NM_024426.6(WT1):c.587G>A (p.Gly196Asp)	LOC107982234, WT1 (G196D)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +6 more	GConflicting classifications of pathogenicity
Select item 304422	NM_024426.6(WT1):c.695G>C (p.Ser232Thr)	WT1 (S15T +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +5 more	GConflicting classifications of pathogenicity
Select item 304421	NM_024426.6(WT1):c.887+4G>A	WT1	Single nucleotide variant (intron variant)	Drash syndrome +5 more	GConflicting classifications of pathogenicity
Select item 304420	NM_024426.6(WT1):c.1017-15T>C	WT1	Single nucleotide variant (intron variant)	Drash syndrome +5 more	GConflicting classifications of pathogenicity
Select item 304419	NM_024426.6(WT1):c.1198T>C (p.Tyr400His)	WT1 (Y183H +9 more)	Single nucleotide variant (missense variant +1 more)	Nephrotic syndrome, type 4 +6 more	GConflicting classifications of pathogenicity
Select item 304418	NM_024426.6(WT1):c.1200C>T (p.Tyr400=)	WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +6 more	GConflicting classifications of pathogenicity
Select item 304417	NM_024426.6(WT1):c.*16G>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephrotic syndrome, type 4 +5 more	GBenign/Likely benign
Select item 304416	NM_024426.6(WT1):c.*88A>G	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Wilms tumor 1 +5 more	GBenign
Select item 304415	NM_024426.6(WT1):c.*110C>T	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Meacham syndrome +2 more	GUncertain significance
Select item 304414	NM_024426.6(WT1):c.*138G>A	WT1	Single nucleotide variant (3 prime UTR variant +1 more)	Nephroblastoma +3 more	GLikely benign

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