"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC107982 - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 257619	NM_024426.6(WT1):c.662-1928_662-1927del	LOC107982234, WT1	Deletion (5 prime UTR variant +1 more)	not specified +6 more	GBenign
Select item 2628421	NM_024426.6(WT1):c.619del (p.Leu207fs)	LOC107982234, WT1 (L207fs)	Deletion (frameshift variant +1 more)	WT1-related disorder	GPathogenic
Select item 406686	NM_024426.6(WT1):c.615C>G (p.Pro205=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	WT1-related disorder +4 more	GLikely benign
Select item 261713	NM_024426.6(WT1):c.609C>T (p.Asn203=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not specified +9 more	GBenign
Select item 241483	NM_024426.6(WT1):c.543C>T (p.Arg181=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +9 more	GBenign/Likely benign
Select item 261712	NM_024426.6(WT1):c.513C>A (p.Gly171=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not specified +8 more	GBenign/Likely benign
Select item 1541965	NM_024426.6(WT1):c.456C>A (p.Gly152=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +4 more	GLikely benign
Select item 3042901	NM_024426.6(WT1):c.390A>C (p.Pro130=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	WT1-related disorder	GLikely benign
Select item 2630893	NM_024426.6(WT1):c.381del (p.Ala128fs)	LOC107982234, WT1 (A128fs)	Deletion (frameshift variant +1 more)	WT1-related disorder	GPathogenic
Select item 261711	NM_024426.6(WT1):c.381C>G (p.Pro127=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +8 more	GConflicting classifications of pathogenicity
Select item 241481	NM_024426.6(WT1):c.375C>T (p.Gly125=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +8 more	GConflicting classifications of pathogenicity
Select item 193454	NM_024426.6(WT1):c.345C>T (p.Pro115=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Nephroblastoma +8 more	GBenign
Select item 406682	NM_024426.6(WT1):c.286G>A (p.Gly96Ser)	LOC107982234, WT1 (G96S)	Single nucleotide variant (missense variant +1 more)	WT1-related disorder +4 more	GUncertain significance
Select item 2177953	NM_024426.6(WT1):c.261C>A (p.Ala87=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +4 more	GConflicting classifications of pathogenicity
Select item 241479	NM_024426.6(WT1):c.216G>T (p.Gln72His)	LOC107982234, WT1 (Q72H)	Single nucleotide variant (missense variant +1 more)	Wilms tumor 1 +8 more	GBenign/Likely benign
Select item 261710	NM_024426.6(WT1):c.213G>T (p.Pro71=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not specified +8 more	GBenign
Select item 241476	NM_024426.6(WT1):c.181C>A (p.Arg61=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not provided +9 more	GBenign/Likely benign
Select item 304428	NM_024426.6(WT1):c.174C>G (p.Leu58=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Nephrotic syndrome, type 4 +8 more	GConflicting classifications of pathogenicity
Select item 265295	NM_024426.6(WT1):c.151del (p.Ala51fs)	LOC107982234, WT1 (A51fs)	Deletion (frameshift variant +1 more)	Drash syndrome +6 more	GConflicting classifications of pathogenicity
Select item 2630917	NM_024426.6(WT1):c.145G>C (p.Gly49Arg)	LOC107982234, WT1 (G44R +1 more)	Single nucleotide variant (missense variant +1 more)	WT1-related disorder	GUncertain significance
Select item 193453	NM_024426.6(WT1):c.123G>C (p.Pro41=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not specified +9 more	GBenign/Likely benign
Select item 1113148	NM_024426.6(WT1):c.99A>G (p.Pro33=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +4 more	GLikely benign
Select item 543158	NM_024426.6(WT1):c.75C>T (p.Ser25=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	WT1-related disorder +4 more	GLikely benign
Select item 802670	NM_024426.6(WT1):c.28G>T (p.Ala10Ser)	LOC107982234, WT1 (A10S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +5 more	GUncertain significance
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 2026335	NM_024426.6(WT1):c.24C>T (p.Asp8=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +4 more	GLikely benign
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

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Items: 27