ClinVar for MedGen (Select 347366) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1802156	NM_025216.3(WNT10A):c.[487C>T];[682T>A]			Odonto-onycho-dermal dysplasia	GPathogenic
Select item 1174863	NM_025216.3(WNT10A):c.347T>C (p.Ile116Thr)	WNT10A (I116T)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +2 more	GConflicting classifications of pathogenicity
Select item 1153585	NM_025216.3(WNT10A):c.125A>G (p.Asn42Ser)	WNT10A (N42S)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 1127314	NM_025216.3(WNT10A):c.1146C>T (p.Asn382=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 1119678	NM_025216.3(WNT10A):c.402C>T (p.Tyr134=)	WNT10A	Single nucleotide variant (synonymous variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GLikely benign
Select item 1109829	NM_025216.3(WNT10A):c.745G>A (p.Val249Ile)	WNT10A (V249I)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 1104959	NM_025216.3(WNT10A):c.775C>A (p.Arg259=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 1087106	NM_025216.3(WNT10A):c.966G>C (p.Pro322=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 1042413	NM_025216.3(WNT10A):c.519G>T (p.Lys173Asn)	WNT10A (K173N)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +1 more	GUncertain significance
Select item 989509	NM_025216.3(WNT10A):c.1162C>T (p.Arg388Cys)	WNT10A (R388C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 985708	NM_025216.3(WNT10A):c.958C>T (p.Pro320Ser)	WNT10A (P320S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 972612	NM_025216.3(WNT10A):c.427C>T (p.His143Tyr)	WNT10A (H143Y)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 969520	NM_025216.3(WNT10A):c.914G>A (p.Arg305His)	WNT10A (R305H)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
Select item 965475	NM_025216.3(WNT10A):c.796G>A (p.Gly266Ser)	WNT10A (G266S)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +1 more	GUncertain significance
Select item 947689	NM_025216.3(WNT10A):c.1124T>G (p.Met375Arg)	WNT10A (M375R)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +1 more	GUncertain significance
Select item 936775	NM_025216.3(WNT10A):c.376+1G>A	WNT10A	Single nucleotide variant (splice donor variant)	Odonto-onycho-dermal dysplasia +2 more	GPathogenic
Select item 899013	NM_025216.3(WNT10A):c.443C>T (p.Ala148Val)	WNT10A (A148V)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +2 more	GUncertain significance
Select item 898940	NM_025216.3(WNT10A):c.-70G>C	LOC129935619, WNT10A	Single nucleotide variant (5 prime UTR variant)	Odonto-onycho-dermal dysplasia +2 more	GUncertain significance
Select item 898153	NM_025216.3(WNT10A):c.*339C>T	WNT10A	Single nucleotide variant (3 prime UTR variant)	Odonto-onycho-dermal dysplasia +2 more	GUncertain significance
Select item 898152	NM_025216.3(WNT10A):c.*238C>T	WNT10A	Single nucleotide variant (3 prime UTR variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
Select item 898019	NM_025216.3(WNT10A):c.719C>T (p.Ala240Val)	WNT10A (A240V)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +2 more	GConflicting classifications of pathogenicity
Select item 897867	NM_025216.3(WNT10A):c.377-11T>C	WNT10A	Single nucleotide variant (intron variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GConflicting classifications of pathogenicity
Select item 897866	NM_025216.3(WNT10A):c.364A>T (p.Ile122Phe)	WNT10A (I122F)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +2 more	GUncertain significance
Select item 897794	NM_025216.3(WNT10A):c.-123C>A	LOC129935619, WNT10A	Single nucleotide variant (5 prime UTR variant)	Odonto-onycho-dermal dysplasia +2 more	GUncertain significance
Select item 896531	NM_025216.3(WNT10A):c.*139C>G	WNT10A	Single nucleotide variant (3 prime UTR variant)	Odonto-onycho-dermal dysplasia +2 more	GUncertain significance
Select item 896458	NM_025216.3(WNT10A):c.1035C>A (p.Phe345Leu)	WNT10A (F345L)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +2 more	GUncertain significance
Select item 896390	NM_025216.3(WNT10A):c.697G>A (p.Glu233Lys)	WNT10A (E233K)	Single nucleotide variant (missense variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GConflicting classifications of pathogenicity
Select item 896389	NM_025216.3(WNT10A):c.694C>T (p.Arg232Trp)	WNT10A (R232W)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +2 more	GUncertain significance
Select item 896321	NM_025216.3(WNT10A):c.526C>T (p.Arg176Cys)	WNT10A (R176C)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +2 more	GUncertain significance
Select item 894954	NM_025216.3(WNT10A):c.668G>A (p.Arg223His)	WNT10A (R223H)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +2 more	GUncertain significance
Select item 894953	NM_025216.3(WNT10A):c.664G>A (p.Glu222Lys)	WNT10A (E222K)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
Select item 894952	NM_025216.3(WNT10A):c.653T>G (p.Met218Arg)	WNT10A (M218R)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
Select item 894882	NM_025216.3(WNT10A):c.483G>C (p.Ala161=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +2 more	GConflicting classifications of pathogenicity
Select item 894811	NM_025216.3(WNT10A):c.166A>G (p.Asn56Asp)	WNT10A (N56D)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
Select item 841749	NM_025216.3(WNT10A):c.814C>T (p.Gln272Ter)	WNT10A (Q272*)	Single nucleotide variant (nonsense)	not provided +3 more	GPathogenic/Likely pathogenic
Select item 797893	NM_025216.3(WNT10A):c.957G>T (p.Ser319=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 794711	NM_025216.3(WNT10A):c.891C>G (p.Ala297=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 766991	NM_025216.3(WNT10A):c.801G>A (p.Thr267=)	WNT10A	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 766887	NM_025216.3(WNT10A):c.874A>G (p.Ser292Gly)	WNT10A (S292G)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 762360	NM_025216.3(WNT10A):c.1005C>T (p.Asp335=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +2 more	GLikely benign
Select item 743353	NM_025216.3(WNT10A):c.444G>A (p.Ala148=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 739829	NM_025216.3(WNT10A):c.591C>T (p.Ala197=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GBenign
Select item 723234	NM_025216.3(WNT10A):c.429C>T (p.His143=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 707602	NM_025216.3(WNT10A):c.4G>A (p.Gly2Ser)	WNT10A (G2S)	Single nucleotide variant (missense variant)	not provided +2 more	GLikely benign
Select item 707156	NM_025216.3(WNT10A):c.512G>A (p.Arg171His)	WNT10A (R171H)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 705211	NM_025216.3(WNT10A):c.534A>G (p.Gln178=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +2 more	GBenign/Likely benign
Select item 704869	NM_025216.3(WNT10A):c.234C>T (p.His78=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +2 more	GBenign/Likely benign
Select item 702777	NM_025216.3(WNT10A):c.660C>T (p.Phe220=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 639357	NM_025216.3(WNT10A):c.694del (p.Arg232fs)	WNT10A (R232fs)	Deletion (frameshift variant)	not provided +3 more	GPathogenic/Likely pathogenic
Select item 582506	NM_025216.3(WNT10A):c.205C>T (p.Arg69Trp)	WNT10A (R69W)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +1 more	GUncertain significance
Select item 582420	NM_025216.3(WNT10A):c.695G>A (p.Arg232Gln)	WNT10A (R232Q)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +1 more	GUncertain significance
Select item 579717	NM_025216.3(WNT10A):c.987_989dup (p.Arg330dup)	WNT10A	Duplication (inframe_insertion)	Tooth agenesis, selective, 4 +1 more	GUncertain significance
Select item 574455	NM_025216.3(WNT10A):c.403G>A (p.Ala135Thr)	WNT10A (A135T)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +1 more	GUncertain significance
Select item 532830	NM_025216.3(WNT10A):c.831G>T (p.Trp277Cys)	WNT10A (W277C)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +1 more	GUncertain significance
Select item 532829	NM_025216.3(WNT10A):c.910A>C (p.Asn304His)	WNT10A (N304H)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +1 more	GPathogenic
Select item 464182	NM_025216.3(WNT10A):c.433G>A (p.Val145Met)	WNT10A (V145M)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +1 more	GPathogenic/Likely pathogenic
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 464180	NM_025216.3(WNT10A):c.216G>T (p.Met72Ile)	WNT10A (M72I)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +1 more	GUncertain significance
Select item 417898	NM_025216.3(WNT10A):c.616C>T (p.Gln206Ter)	WNT10A (Q206*)	Single nucleotide variant (nonsense)	Odonto-onycho-dermal dysplasia +2 more	GLikely pathogenic
Select item 373902	NM_025216.3(WNT10A):c.667C>T (p.Arg223Cys)	WNT10A (R223C)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 334423	NM_025216.3(WNT10A):c.*441C>T	WNT10A	Single nucleotide variant (3 prime UTR variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
Select item 334422	NM_025216.3(WNT10A):c.*431C>T	WNT10A	Single nucleotide variant (3 prime UTR variant)	SchC6pf-Schulz-Passarge syndrome +3 more	GBenign/Likely benign
Select item 334421	NM_025216.3(WNT10A):c.*275C>T	WNT10A	Single nucleotide variant (3 prime UTR variant)	Odonto-onycho-dermal dysplasia +2 more	GLikely benign
Select item 334420	NM_025216.3(WNT10A):c.*216G>C	WNT10A	Single nucleotide variant (3 prime UTR variant)	Tooth agenesis, selective, 4 +2 more	GLikely benign
Select item 334419	NM_025216.3(WNT10A):c.*128T>C	WNT10A	Single nucleotide variant (3 prime UTR variant)	Tooth agenesis, selective, 4 +2 more	GLikely benign
Select item 334418	NM_025216.3(WNT10A):c.*115C>T	WNT10A	Single nucleotide variant (3 prime UTR variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
Select item 334417	NM_025216.3(WNT10A):c.*108G>A	WNT10A	Single nucleotide variant (3 prime UTR variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
Select item 334416	NM_025216.3(WNT10A):c.*15C>T	LOC129935625, WNT10A	Single nucleotide variant (3 prime UTR variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
Select item 334415	NM_025216.3(WNT10A):c.1134C>T (p.Gly378=)	WNT10A	Single nucleotide variant (synonymous variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GConflicting classifications of pathogenicity
Select item 334414	NM_025216.3(WNT10A):c.1087A>C (p.Asn363His)	WNT10A (N363H)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +4 more	GConflicting classifications of pathogenicity
Select item 334413	NM_025216.3(WNT10A):c.1061C>T (p.Ser354Leu)	WNT10A (S354L)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
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 334411	NM_025216.3(WNT10A):c.1017C>T (p.Phe339=)	WNT10A	Single nucleotide variant (synonymous variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GConflicting classifications of pathogenicity
Select item 334410	NM_025216.3(WNT10A):c.1003G>A (p.Asp335Asn)	WNT10A (D335N)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +2 more	GBenign/Likely benign
Select item 334409	NM_025216.3(WNT10A):c.918C>G (p.Asn306Lys)	WNT10A (N306K)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +2 more	GLikely benign
Select item 334408	NM_025216.3(WNT10A):c.841C>G (p.Pro281Ala)	WNT10A (P281A)	Single nucleotide variant (missense variant)	SchC6pf-Schulz-Passarge syndrome +3 more	GUncertain significance
Select item 334407	NM_025216.3(WNT10A):c.841C>A (p.Pro281Thr)	WNT10A (P281T)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 334406	NM_025216.3(WNT10A):c.838A>T (p.Thr280Ser)	WNT10A (T280S)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
Select item 334405	NM_025216.3(WNT10A):c.817C>A (p.Leu273Ile)	WNT10A (L273I)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +2 more	GBenign
Select item 334404	NM_025216.3(WNT10A):c.756+14C>T	WNT10A	Single nucleotide variant (intron variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GConflicting classifications of pathogenicity
Select item 334403	NM_025216.3(WNT10A):c.756+13C>A	WNT10A	Single nucleotide variant (intron variant)	Tooth agenesis, selective, 4 +2 more	GConflicting classifications of pathogenicity
Select item 334402	NM_025216.3(WNT10A):c.652A>G (p.Met218Val)	WNT10A (M218V)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +4 more	GConflicting classifications of pathogenicity
Select item 334401	NM_025216.3(WNT10A):c.551G>A (p.Arg184His)	WNT10A (R184H)	Single nucleotide variant (missense variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GConflicting classifications of pathogenicity
Select item 334400	NM_025216.3(WNT10A):c.498C>T (p.Asp166=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +2 more	GConflicting classifications of pathogenicity
Select item 334399	NM_025216.3(WNT10A):c.493G>A (p.Gly165Arg)	WNT10A (G165R)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 334398	NM_025216.3(WNT10A):c.437C>G (p.Ser146Cys)	WNT10A (S146C)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
Select item 334397	NM_025216.3(WNT10A):c.420C>T (p.Gly140=)	WNT10A	Single nucleotide variant (synonymous variant)	SchC6pf-Schulz-Passarge syndrome +3 more	GLikely benign
Select item 334396	NM_025216.3(WNT10A):c.349C>T (p.Pro117Ser)	WNT10A (P117S)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
Select item 334395	NM_025216.3(WNT10A):c.315G>C (p.Trp105Cys)	WNT10A (W105C)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +2 more	GUncertain significance
Select item 334394	NM_025216.3(WNT10A):c.208C>T (p.Arg70Trp)	WNT10A (R70W)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 334393	NM_025216.3(WNT10A):c.149C>T (p.Pro50Leu)	WNT10A (P50L)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +2 more	GConflicting classifications of pathogenicity
Select item 334392	NM_025216.3(WNT10A):c.85C>T (p.Leu29=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +2 more	GBenign
Select item 334391	NM_025216.2(WNT10A):c.-149G>T	LOC129935619, WNT10A	Single nucleotide variant (genic upstream transcript variant)	not provided +3 more	GUncertain significance
Select item 334390	NM_025216.2(WNT10A):c.-153G>A	LOC129935619, WNT10A	Single nucleotide variant (genic upstream transcript variant)	Selective tooth agenesis +2 more	GUncertain significance
Select item 334389	NM_025216.2(WNT10A):c.-194dup	LOC129935619, WNT10A	Duplication (genic upstream transcript variant)	Selective tooth agenesis +2 more	GUncertain significance
Select item 334388	NM_025216.2(WNT10A):c.-202G>C	LOC129935619, WNT10A	Single nucleotide variant (genic upstream transcript variant)	Selective tooth agenesis +2 more	GUncertain significance
Select item 334387	NM_025216.2(WNT10A):c.-203dup	LOC129935619, WNT10A	Duplication (genic upstream transcript variant)	Selective tooth agenesis +2 more	GLikely benign
Select item 334386	NM_025216.2(WNT10A):c.-249G>C	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	Selective tooth agenesis +3 more	GUncertain significance
Select item 334385	NM_025216.2(WNT10A):c.-270G>C	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	Selective tooth agenesis +2 more	GUncertain significance
Select item 334384	NM_025216.2(WNT10A):c.-285C>T	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	Selective tooth agenesis +2 more	GUncertain significance

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