"GeneDx"[submitter] AND "WNT10A"[gene] - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59159	GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3	AAMP, ABCA12 +1665 more	Copy number gain	See cases	GPathogenic
Select item 1259665	NM_025216.3(WNT10A):c.114-56T>C	WNT10A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2430419	NM_025216.3(WNT10A):c.131T>C (p.Ile44Thr)	WNT10A (I44T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 334394	NM_025216.3(WNT10A):c.208C>T (p.Arg70Trp)	WNT10A (R70W)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +4 more	GConflicting classifications of pathogenicity
Select item 423769	NM_025216.3(WNT10A):c.242T>C (p.Val81Ala)	WNT10A (V81A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 68843	NM_025216.3(WNT10A):c.283G>A (p.Glu95Lys)	WNT10A (E95K)	Single nucleotide variant (missense variant)	WNT10A-related condition +3 more	GConflicting classifications of pathogenicity
Select item 532827	NM_025216.3(WNT10A):c.310C>T (p.Arg104Cys)	WNT10A (R104C)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +2 more	GConflicting classifications of pathogenicity
Select item 633837	NM_025216.3(WNT10A):c.311G>A (p.Arg104His)	WNT10A (R104H)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +2 more	GConflicting classifications of pathogenicity
Select item 4461	NM_025216.3(WNT10A):c.321C>A (p.Cys107Ter)	WNT10A (C107*)	Single nucleotide variant (nonsense)	Odonto-onycho-dermal dysplasia +7 more	GPathogenic
Select item 372548	NM_025216.3(WNT10A):c.337C>T (p.Arg113Cys)	WNT10A (R113C)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +3 more	GConflicting classifications of pathogenicity
Select item 464181	NM_025216.3(WNT10A):c.382C>T (p.Arg128Ter)	WNT10A (R128*)	Single nucleotide variant (nonsense)	Tooth agenesis, selective, 4 +3 more	GPathogenic/Likely pathogenic
Select item 4463	NM_025216.3(WNT10A):c.383G>A (p.Arg128Gln)	WNT10A (R128Q)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +2 more	GPathogenic/Likely pathogenic
Select item 265292	NM_025216.3(WNT10A):c.391G>A (p.Ala131Thr)	WNT10A (A131T)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +3 more	GPathogenic/Likely pathogenic
Select item 1105615	NM_025216.3(WNT10A):c.408C>G (p.Ile136Met)	WNT10A (I136M)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1305315	NM_025216.3(WNT10A):c.430G>C (p.Ala144Pro)	WNT10A (A144P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 189351	NM_025216.3(WNT10A):c.487C>T (p.Arg163Trp)	WNT10A (R163W)	Single nucleotide variant (missense variant)	WNT10A-related condition +4 more	GConflicting classifications of pathogenicity
Select item 334399	NM_025216.3(WNT10A):c.493G>A (p.Gly165Arg)	WNT10A (G165R)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +4 more	GConflicting classifications of pathogenicity
Select item 225515	NM_025216.3(WNT10A):c.511C>T (p.Arg171Cys)	WNT10A (R171C)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 2 +4 more	GConflicting classifications of pathogenicity
Select item 139576	NM_025216.3(WNT10A):c.637G>A (p.Gly213Ser)	WNT10A (G213S)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +4 more	GConflicting classifications of pathogenicity
Select item 379584	NM_025216.3(WNT10A):c.650A>G (p.Asp217Gly)	WNT10A (D217G)	Single nucleotide variant (missense variant)	not provided	GPathogenic
Select item 427045	NM_025216.3(WNT10A):c.661G>A (p.Gly221Arg)	WNT10A (G221R)	Single nucleotide variant (missense variant)	WNT10A-related condition +4 more	GConflicting classifications of pathogenicity
Select item 4462	NM_025216.3(WNT10A):c.682T>A (p.Phe228Ile)	WNT10A (F228I)	Single nucleotide variant (missense variant)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 2502114	NM_025216.3(WNT10A):c.684T>G (p.Phe228Leu)	WNT10A (F228L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 265293	NM_025216.3(WNT10A):c.742C>T (p.Arg248Ter)	WNT10A (R248*)	Single nucleotide variant (nonsense)	WNT10A-related condition +4 more	GPathogenic
Select item 265294	NM_025216.3(WNT10A):c.803C>G (p.Ser268Ter)	WNT10A (S268*)	Single nucleotide variant (nonsense)	Tooth agenesis, selective, 4 +3 more	GPathogenic
Select item 1307968	NM_025216.3(WNT10A):c.862G>A (p.Ala288Thr)	WNT10A (A288T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1304217	NM_025216.3(WNT10A):c.937G>C (p.Gly313Arg)	WNT10A (G313R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 280404	NM_025216.3(WNT10A):c.985dup (p.Arg329fs)	WNT10A (R329fs)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 334412	NM_025216.3(WNT10A):c.1049C>T (p.Pro350Leu)	WNT10A (P350L)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +3 more	GUncertain significance
Select item 432003	NM_025216.3(WNT10A):c.1084T>C (p.Cys362Arg)	WNT10A (C362R)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +2 more	GPathogenic/Likely pathogenic
Select item 334414	NM_025216.3(WNT10A):c.1087A>C (p.Asn363His)	WNT10A (N363H)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +4 more	GConflicting classifications of pathogenicity
Select item 950198	NM_025216.3(WNT10A):c.1114T>G (p.Cys372Gly)	WNT10A (C372G)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2661938	NM_025216.3(WNT10A):c.1151T>A (p.Leu384Gln)	WNT10A (L384Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 378862	NM_025216.3(WNT10A):c.1168G>T (p.Glu390Ter)	WNT10A (E390*)	Single nucleotide variant (nonsense)	not provided +2 more	GPathogenic/Likely pathogenic
Select item 427218	NM_025216.3(WNT10A):c.1247G>A (p.Cys416Tyr)	LOC129935625, WNT10A (C416Y)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic

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Items: 35