ClinVar for Gene (Select 80326) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3374860	NM_025216.3(WNT10A):c.286T>C (p.Cys96Arg)	WNT10A (C96R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3366486	NM_025216.3(WNT10A):c.827G>T (p.Cys276Phe)	WNT10A (C276F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3366404	NM_025216.3(WNT10A):c.409G>A (p.Ala137Thr)	WNT10A (A137T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3360178	NM_025216.3(WNT10A):c.152C>G (p.Pro51Arg)	WNT10A (P51R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3357097	NM_025216.3(WNT10A):c.390C>G (p.Ser130Arg)	WNT10A (S130R)	Single nucleotide variant (missense variant)	WNT10A-related disorder	GUncertain significance
Select item 3333195	NM_025216.3(WNT10A):c.599C>G (p.Thr200Arg)	WNT10A (T200R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3333194	NM_025216.3(WNT10A):c.320G>A (p.Cys107Tyr)	WNT10A (C107Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3333193	NM_025216.3(WNT10A):c.789G>C (p.Lys263Asn)	WNT10A (K263N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3333192	NM_025216.3(WNT10A):c.19C>A (p.Arg7Ser)	WNT10A (R7S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3251508	NM_025216.3(WNT10A):c.206G>A (p.Arg69Gln)	WNT10A (R69Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3247494	NC_000002.11:g.(?_219646906)_(219942948_?)dup	CDK5R2, CFAP65 +9 more	Duplication	not provided	GUncertain significance
Select item 3247231	NC_000002.11:g.(?_219754812)_(219757475_?)del	WNT10A	Deletion	Odonto-onycho-dermal dysplasia +1 more	GPathogenic
Select item 3242353	NM_025216.3(WNT10A):c.62delinsGA (p.Ala21fs)	WNT10A (A21fs)	Indel (frameshift variant)	Odonto-onycho-dermal dysplasia	GPathogenic
Select item 3233578	NM_025216.3(WNT10A):c.311G>C (p.Arg104Pro)	WNT10A (R104P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190705	NM_025216.3(WNT10A):c.967G>A (p.Gly323Ser)	WNT10A (G323S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3190704	NM_025216.3(WNT10A):c.929T>G (p.Leu310Arg)	WNT10A (L310R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3190702	NM_025216.3(WNT10A):c.729G>C (p.Arg243Ser)	WNT10A (R243S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3190701	NM_025216.3(WNT10A):c.230G>A (p.Arg77His)	WNT10A (R77H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3190700	NM_025216.3(WNT10A):c.200T>C (p.Leu67Pro)	WNT10A (L67P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3190699	NM_025216.3(WNT10A):c.1052G>T (p.Arg351Leu)	WNT10A (R351L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3148939	GRCh37/hg19 2q35-37.3(chr2:216815496-242782258)x3	AAMP, ABCB6 +218 more	Copy number gain	See cases	GPathogenic
Select item 3054374	NM_025216.3(WNT10A):c.294C>T (p.His98=)	WNT10A	Single nucleotide variant (synonymous variant)	WNT10A-related disorder	GLikely benign
Select item 3039373	NM_025216.3(WNT10A):c.532_537delinsA (p.Gln178fs)	WNT10A (Q178fs)	Indel (frameshift variant)	WNT10A-related disorder	GPathogenic
Select item 3032893	NM_025216.3(WNT10A):c.460C>A (p.Leu154Met)	WNT10A (L154M)	Single nucleotide variant (missense variant)	WNT10A-related disorder	GUncertain significance
Select item 2954549	NM_025216.3(WNT10A):c.757-16G>A	WNT10A	Single nucleotide variant (intron variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2954365	NM_025216.3(WNT10A):c.105C>G (p.Ala35=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2954237	NM_025216.3(WNT10A):c.1127G>C (p.Cys376Ser)	WNT10A (C376S)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +1 more	GUncertain significance
Select item 2954086	NM_025216.3(WNT10A):c.1218G>A (p.Glu406=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2953943	NM_025216.3(WNT10A):c.219G>A (p.Glu73=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2953691	NM_025216.3(WNT10A):c.376+19T>C	WNT10A	Single nucleotide variant (intron variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2953659	NM_025216.3(WNT10A):c.956C>A (p.Ser319Ter)	WNT10A (S319*)	Single nucleotide variant (nonsense)	Odonto-onycho-dermal dysplasia +1 more	GPathogenic
Select item 2952209	NM_025216.3(WNT10A):c.1155C>T (p.Arg385=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2952066	NM_025216.3(WNT10A):c.1081C>T (p.Leu361=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2951734	NM_025216.3(WNT10A):c.342C>T (p.Asn114=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2951243	NM_025216.3(WNT10A):c.251dup (p.Ala85fs)	WNT10A (A85fs)	Duplication (frameshift variant)	Odonto-onycho-dermal dysplasia +1 more	GPathogenic
Select item 2950893	NM_025216.3(WNT10A):c.243G>A (p.Val81=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2950751	NM_025216.3(WNT10A):c.381_382delinsTT (p.Arg128Ter)	WNT10A (R128*)	Indel (nonsense)	Odonto-onycho-dermal dysplasia +1 more	GPathogenic
Select item 2949508	NM_025216.3(WNT10A):c.801G>T (p.Thr267=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2949194	NM_025216.3(WNT10A):c.78G>T (p.Leu26=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2949031	NM_025216.3(WNT10A):c.306C>T (p.Asp102=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2948518	NM_025216.3(WNT10A):c.694dup (p.Arg232fs)	WNT10A (R232fs)	Duplication (frameshift variant)	Odonto-onycho-dermal dysplasia +1 more	GPathogenic
Select item 2948162	NM_025216.3(WNT10A):c.380del (p.Phe127fs)	WNT10A (F127fs)	Deletion (frameshift variant)	Odonto-onycho-dermal dysplasia +1 more	GPathogenic
Select item 2947766	NM_025216.3(WNT10A):c.903G>T (p.Arg301=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2947618	NM_025216.3(WNT10A):c.981_993dup (p.Ser332fs)	WNT10A (S332fs)	Duplication (frameshift variant)	Odonto-onycho-dermal dysplasia +1 more	GPathogenic
Select item 2947572	NM_025216.3(WNT10A):c.113+7C>A	WNT10A	Single nucleotide variant (intron variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2947564	NM_025216.3(WNT10A):c.844G>T (p.Glu282Ter)	WNT10A (E282*)	Single nucleotide variant (nonsense)	Odonto-onycho-dermal dysplasia +1 more	GPathogenic
Select item 2947310	NM_025216.3(WNT10A):c.576C>G (p.Val192=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2947301	NM_025216.3(WNT10A):c.882C>T (p.Phe294=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2947127	NM_025216.3(WNT10A):c.1053C>G (p.Arg351=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2947030	NM_025216.3(WNT10A):c.152del (p.Pro51fs)	WNT10A (P51fs)	Deletion (frameshift variant)	Odonto-onycho-dermal dysplasia +1 more	GPathogenic
Select item 2946158	NM_025216.3(WNT10A):c.162G>A (p.Val54=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2945944	NM_025216.3(WNT10A):c.813C>A (p.Cys271Ter)	WNT10A (C271*)	Single nucleotide variant (nonsense)	Odonto-onycho-dermal dysplasia +1 more	GPathogenic
Select item 2945642	NM_025216.3(WNT10A):c.59C>A (p.Pro20Gln)	WNT10A (P20Q)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +1 more	GUncertain significance
Select item 2944959	NM_025216.3(WNT10A):c.376+13_376+14insCTTTCTTTCCAAGTTATGGATGTCCATTGTGTGGGGTCAGGTGACCTCCGTTTCCTCCA	WNT10A	Insertion (intron variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2943998	NM_025216.3(WNT10A):c.640T>C (p.Cys214Arg)	WNT10A (C214R)	Single nucleotide variant (missense variant)	Odonto-onycho-dermal dysplasia +1 more	GUncertain significance
Select item 2943978	NM_025216.3(WNT10A):c.33G>A (p.Arg11=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2943454	NM_025216.3(WNT10A):c.111C>T (p.Pro37=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2943271	NM_025216.3(WNT10A):c.78G>A (p.Leu26=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2943208	NM_025216.3(WNT10A):c.1206G>C (p.Val402=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2942392	NM_025216.3(WNT10A):c.462G>T (p.Leu154=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2942022	NM_025216.3(WNT10A):c.462G>A (p.Leu154=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2941982	NM_025216.3(WNT10A):c.309G>A (p.Gln103=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2941649	NM_025216.3(WNT10A):c.1011C>T (p.Val337=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2941228	NM_025216.3(WNT10A):c.174C>T (p.Asn58=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2940942	NM_025216.3(WNT10A):c.1101C>A (p.Ala367=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2940789	NM_025216.3(WNT10A):c.762G>A (p.Val254=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2940532	NM_025216.3(WNT10A):c.63G>T (p.Ala21=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2940359	NM_025216.3(WNT10A):c.99_105dup (p.Met36fs)	WNT10A (M36fs)	Duplication (frameshift variant)	Tooth agenesis, selective, 4 +1 more	GPathogenic
Select item 2939198	NM_025216.3(WNT10A):c.795C>T (p.His265=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2939138	NM_025216.3(WNT10A):c.542C>T (p.Ala181Val)	WNT10A (A181V)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +1 more	GUncertain significance
Select item 2937850	NM_025216.3(WNT10A):c.1179C>T (p.His393=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2937522	NM_025216.3(WNT10A):c.663G>A (p.Gly221=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2937474	NM_025216.3(WNT10A):c.376+8C>T	WNT10A	Single nucleotide variant (intron variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2937441	NM_025216.3(WNT10A):c.507C>T (p.Ala169=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2937327	NM_025216.3(WNT10A):c.5_27del (p.Gly2fs)	WNT10A (G2fs)	Deletion (frameshift variant +1 more)	Tooth agenesis, selective, 4 +1 more	GPathogenic
Select item 2936872	NM_025216.3(WNT10A):c.720G>T (p.Ala240=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2936322	NM_025216.3(WNT10A):c.966G>A (p.Pro322=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2936230	NM_025216.3(WNT10A):c.843C>G (p.Pro281=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2935630	NM_025216.3(WNT10A):c.756+17del	WNT10A	Deletion (intron variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2935088	NM_025216.3(WNT10A):c.756+15C>A	WNT10A	Single nucleotide variant (intron variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2935071	NM_025216.3(WNT10A):c.377-18C>G	WNT10A	Single nucleotide variant (intron variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2934164	NM_025216.3(WNT10A):c.1041G>A (p.Glu347=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2933866	NM_025216.3(WNT10A):c.1120_1134dup (p.Gly378_Arg379insSerMetCysCysGly)	WNT10A	Duplication (inframe_insertion)	Odonto-onycho-dermal dysplasia +1 more	GUncertain significance
Select item 2933347	NM_025216.3(WNT10A):c.756+18G>A	WNT10A	Single nucleotide variant (intron variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2933323	NM_025216.3(WNT10A):c.114-8G>A	WNT10A	Single nucleotide variant (intron variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2933202	NM_025216.3(WNT10A):c.741C>T (p.Asn247=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2933018	NM_025216.3(WNT10A):c.757-17G>T	WNT10A	Single nucleotide variant (intron variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2932609	NM_025216.3(WNT10A):c.435G>A (p.Val145=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2932532	NM_025216.3(WNT10A):c.208C>A (p.Arg70=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2931898	NM_025216.3(WNT10A):c.21C>G (p.Arg7=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2931867	NM_025216.3(WNT10A):c.858G>C (p.Val286=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2931680	NM_025216.3(WNT10A):c.69G>A (p.Trp23Ter)	WNT10A (W23*)	Single nucleotide variant (nonsense)	Tooth agenesis, selective, 4 +1 more	GPathogenic
Select item 2931638	NM_025216.3(WNT10A):c.927G>A (p.Gln309=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2931159	NM_025216.3(WNT10A):c.376+17C>A	WNT10A	Single nucleotide variant (intron variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2930676	NM_025216.3(WNT10A):c.1167C>T (p.Ser389=)	WNT10A	Single nucleotide variant (synonymous variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2930675	NM_025216.3(WNT10A):c.981G>A (p.Pro327=)	WNT10A	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 2930015	NM_025216.3(WNT10A):c.376+18C>A	WNT10A	Single nucleotide variant (intron variant)	Odonto-onycho-dermal dysplasia +1 more	GLikely benign
Select item 2928912	NM_025216.3(WNT10A):c.75C>T (p.Leu25=)	WNT10A	Single nucleotide variant (synonymous variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2928863	NM_025216.3(WNT10A):c.757-20C>A	WNT10A	Single nucleotide variant (intron variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign
Select item 2928340	NM_025216.3(WNT10A):c.114-10A>G	WNT10A	Single nucleotide variant (intron variant)	Tooth agenesis, selective, 4 +1 more	GLikely benign

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