C0950122[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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Items: 74

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 +9 more	GUncertain significance
Select item 578607	NM_024426.6(WT1):c.1478G>A (p.Ser493Asn)	WT1 (S273N +13 more)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +3 more	GUncertain significance
Select item 3493	NM_024426.6(WT1):c.1447+5G>A	WT1	Single nucleotide variant (intron variant)	not provided +9 more	GPathogenic
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 +10 more	GPathogenic/Likely pathogenic
Select item 3487	NM_024426.6(WT1):c.1399C>T (p.Arg467Trp)	WT1 (R250W +9 more)	Single nucleotide variant (missense variant +1 more)	not provided +9 more	GPathogenic/Likely pathogenic
Select item 3488	NM_024426.6(WT1):c.1316G>A (p.Arg439His)	WT1 (R222H +8 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +8 more	GPathogenic
Select item 406697	NM_024426.6(WT1):c.1211A>C (p.Asn404Thr)	WT1 (N187T +9 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +4 more	GUncertain significance
Select item 135455	NM_024426.6(WT1):c.1154G>A (p.Arg385Gln)	WT1 (R168Q +8 more)	Single nucleotide variant (missense variant +2 more)	not specified +6 more	GConflicting classifications of pathogenicity
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 1038185	NM_024426.6(WT1):c.1127T>C (p.Val376Ala)	WT1 (V359A +9 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +7 more	GUncertain significance
Select item 581178	NM_024426.6(WT1):c.1124G>C (p.Arg375Pro)	WT1 (R158P +8 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance
Select item 646456	NM_024426.6(WT1):c.1123C>T (p.Arg375Cys)	WT1 (R141C +9 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +5 more	GUncertain significance
Select item 476679	NM_024426.6(WT1):c.1121G>A (p.Arg374Gln)	WT1 (R157Q +8 more)	Single nucleotide variant (missense variant +2 more)	Wilms tumor 1 +4 more	GUncertain significance
Select item 1355733	NM_024426.6(WT1):c.1112A>G (p.Gln371Arg)	WT1 (Q137R +9 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance
Select item 406687	NM_024426.6(WT1):c.1100T>G (p.Phe367Cys)	WT1 (F150C +8 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance
Select item 1428489	NM_024426.6(WT1):c.1069G>C (p.Ala357Pro)	WT1 (A123P +9 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance
Select item 2679627	NM_024426.6(WT1):c.992T>C (p.Val331Ala)	WT1 (V114A +4 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +3 more	GUncertain significance
Select item 403610	NM_024426.6(WT1):c.977G>C (p.Gly326Ala)	WT1 (G109A +3 more)	Single nucleotide variant (missense variant +2 more)	not specified +5 more	GUncertain significance
Select item 543137	NM_024426.6(WT1):c.892A>G (p.Asn298Asp)	WT1 (N81D +3 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 656650	NM_024426.6(WT1):c.850G>A (p.Gly284Ser)	WT1 (G67S +4 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 937407	NM_024426.6(WT1):c.830C>T (p.Thr277Ile)	WT1 (T60I +4 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 1470255	NM_024426.6(WT1):c.785-14G>A	WT1	Single nucleotide variant (intron variant)	Frasier syndrome +7 more	GUncertain significance
Select item 476719	NM_024426.6(WT1):c.763A>G (p.Met255Val)	WT1 (M38V +2 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 581447	NM_024426.6(WT1):c.736A>G (p.Asn246Asp)	WT1 (N246D +1 more)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +4 more	GUncertain significance
Select item 656498	NM_024426.6(WT1):c.724G>A (p.Ala242Thr)	WT1 (A242T +2 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 640025	NM_024426.6(WT1):c.710C>T (p.Pro237Leu)	WT1 (P20L +2 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +4 more	GUncertain significance
Select item 476716	NM_024426.6(WT1):c.700G>C (p.Gly234Arg)	WT1 (G17R +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +4 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)	Wilms tumor 1 +8 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)	Frasier syndrome +8 more	GUncertain significance
Select item 577219	NM_024426.6(WT1):c.641A>C (p.Gln214Pro)	LOC107982234, WT1 (Q214P)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 948083	NM_024426.6(WT1):c.638G>A (p.Ser213Asn)	LOC107982234, WT1 (S213N)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 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)	Drash syndrome +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)	not provided +6 more	GUncertain significance
Select item 304423	NM_024426.6(WT1):c.587G>A (p.Gly196Asp)	LOC107982234, WT1 (G196D)	Single nucleotide variant (missense variant +1 more)	Meacham syndrome +6 more	GConflicting classifications of pathogenicity
Select item 582327	NM_024426.6(WT1):c.586G>A (p.Gly196Ser)	LOC107982234, WT1 (G196S)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GUncertain significance
Select item 806643	NM_024426.6(WT1):c.577G>A (p.Ala193Thr)	LOC107982234, WT1 (A193T)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +4 more	GUncertain significance
Select item 951827	NM_024426.6(WT1):c.542G>C (p.Arg181Pro)	LOC107982234, WT1 (R181P)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 2155887	NM_024426.6(WT1):c.541C>G (p.Arg181Gly)	LOC107982234, WT1 (R176G +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 1004708	NM_024426.6(WT1):c.499G>A (p.Val167Ile)	LOC107982234, WT1 (V167I)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 476706	NM_024426.6(WT1):c.475G>A (p.Glu159Lys)	LOC107982234, WT1 (E159K)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +4 more	GUncertain significance
Select item 964352	NM_024426.6(WT1):c.472G>C (p.Glu158Gln)	LOC107982234, WT1 (E158Q)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 840579	NM_024426.6(WT1):c.466C>T (p.Pro156Ser)	LOC107982234, WT1 (P156S)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 1011095	NM_024426.6(WT1):c.449G>A (p.Ser150Asn)	LOC107982234, WT1 (S150N)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 406695	NM_024426.6(WT1):c.439C>G (p.Gln147Glu)	LOC107982234, WT1 (Q147E)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +9 more	GUncertain significance
Select item 2148870	NM_024426.6(WT1):c.413C>T (p.Pro138Leu)	LOC107982234, WT1 (P133L +1 more)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +3 more	GUncertain significance
Select item 1410062	NM_024426.6(WT1):c.406C>A (p.Pro136Thr)	LOC107982234, WT1 (P136T)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 566443	NM_024426.6(WT1):c.397C>A (p.Pro133Thr)	LOC107982234, WT1 (P133T)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GUncertain significance
Select item 1719758	NM_024426.6(WT1):c.391C>A (p.Pro131Thr)	LOC107982234, WT1 (P126T +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 543139	NM_024426.6(WT1):c.355T>C (p.Ser119Pro)	LOC107982234, WT1 (S119P)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 582850	NM_024426.6(WT1):c.352G>A (p.Ala118Thr)	LOC107982234, WT1 (A118T)	Single nucleotide variant (missense variant +1 more)	Frasier syndrome +3 more	GUncertain significance
Select item 543122	NM_024426.6(WT1):c.346C>A (p.Pro116Thr)	LOC107982234, WT1 (P116T)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +4 more	GUncertain significance
Select item 406698	NM_024426.6(WT1):c.343C>T (p.Pro115Ser)	LOC107982234, WT1 (P115S)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +4 more	GUncertain significance
Select item 662247	NM_024426.6(WT1):c.320G>T (p.Trp107Leu)	LOC107982234, WT1 (W107L)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 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)	Drash syndrome +8 more	GConflicting classifications of pathogenicity
Select item 839568	NM_024426.6(WT1):c.305G>A (p.Ser102Asn)	LOC107982234, WT1 (S102N)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 1433146	NM_024426.6(WT1):c.293C>T (p.Ala98Val)	LOC107982234, WT1 (A98V)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 939870	NM_024426.6(WT1):c.293C>G (p.Ala98Gly)	LOC107982234, WT1 (A98G)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 576824	NM_024426.6(WT1):c.277GGC[3] (p.Gly96del)	LOC107982234, WT1 (G96del)	Microsatellite (inframe_deletion +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 1448791	NM_024426.6(WT1):c.240C>G (p.Asp80Glu)	LOC107982234, WT1 (D80E)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 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 543118	NM_024426.6(WT1):c.203G>A (p.Gly68Glu)	LOC107982234, WT1 (G68E)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +8 more	GUncertain significance
Select item 476694	NM_024426.6(WT1):c.200C>G (p.Ser67Cys)	LOC107982234, WT1 (S67C)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GUncertain significance
Select item 1044731	NM_024426.6(WT1):c.197C>A (p.Ala66Glu)	LOC107982234, WT1 (A66E)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +4 more	GUncertain significance
Select item 646844	NM_024426.6(WT1):c.193G>T (p.Gly65Trp)	LOC107982234, WT1 (G65W)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +4 more	GUncertain significance
Select item 2925823	NM_024426.6(WT1):c.182G>A (p.Arg61Gln)	LOC107982234, WT1 (R56Q +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 965853	NM_024426.6(WT1):c.172C>T (p.Leu58Phe)	LOC107982234, WT1 (L58F)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 265295	NM_024426.6(WT1):c.151del (p.Ala51fs)	LOC107982234, WT1 (A51fs)	Deletion (frameshift variant +1 more)	Drash syndrome +5 more	GConflicting classifications of pathogenicity
Select item 543131	NM_024426.6(WT1):c.146G>T (p.Gly49Val)	LOC107982234, WT1 (G49V)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 2202666	NM_024426.6(WT1):c.116G>C (p.Arg39Pro)	LOC107982234, WT1 (R34P +1 more)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 543141	NM_024426.6(WT1):c.77G>A (p.Gly26Glu)	LOC107982234, WT1 (G26E)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +4 more	GUncertain significance
Select item 241484	NM_024426.6(WT1):c.70C>T (p.Arg24Cys)	LOC107982234, WT1 (R24C)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +4 more	GUncertain significance
Select item 1896090	NM_024426.6(WT1):c.32C>T (p.Ser11Phe)	LOC107982234, WT1 (S11F +1 more)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +3 more	GUncertain significance
Select item 1057387	NM_024426.6(WT1):c.32C>G (p.Ser11Cys)	LOC107982234, WT1 (S11C)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +3 more	GUncertain significance
Select item 543119	NM_024426.6(WT1):c.28_29delinsTA (p.Ala10Tyr)	LOC107982234, WT1 (A10Y)	Indel (missense variant +1 more)	Drash syndrome +9 more	GUncertain significance

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Items: 74