ClinVar Miner

List of variants in gene WNT10A reported as uncertain significance for Odonto-onycho-dermal dysplasia; Tooth agenesis, selective, 4

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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_025216.3(WNT10A):c.511C>T (p.Arg171Cys) rs116998555 0.00113
NM_025216.3(WNT10A):c.637G>A (p.Gly213Ser) rs147680216 0.00071
NM_025216.3(WNT10A):c.649G>A (p.Asp217Asn) rs146902156 0.00030
NM_025216.3(WNT10A):c.668G>A (p.Arg223His) rs143424659 0.00028
NM_025216.3(WNT10A):c.487C>T (p.Arg163Trp) rs368280129 0.00019
NM_025216.3(WNT10A):c.216G>T (p.Met72Ile) rs373607885 0.00016
NM_025216.3(WNT10A):c.427C>T (p.His143Tyr) rs202024965 0.00011
NM_025216.3(WNT10A):c.205C>T (p.Arg69Trp) rs200487809 0.00005
NM_025216.3(WNT10A):c.914G>A (p.Arg305His) rs746769946 0.00003
NM_025216.3(WNT10A):c.212A>T (p.Gln71Leu) rs368943130 0.00001
NM_025216.3(WNT10A):c.403G>A (p.Ala135Thr) rs1402990329 0.00001
NM_025216.3(WNT10A):c.443C>T (p.Ala148Val) rs373695499 0.00001
NM_025216.3(WNT10A):c.519G>T (p.Lys173Asn) rs758023820 0.00001
NM_025216.3(WNT10A):c.652A>G (p.Met218Val) rs373991357 0.00001
NM_025216.3(WNT10A):c.670T>C (p.Phe224Leu) rs749857233 0.00001
NM_025216.3(WNT10A):c.695G>A (p.Arg232Gln) rs772154760 0.00001
NM_025216.3(WNT10A):c.697G>A (p.Glu233Lys) rs121908118 0.00001
NM_025216.3(WNT10A):c.756G>A (p.Gln252=) rs768536054 0.00001
NM_025216.3(WNT10A):c.7A>T (p.Ser3Cys) rs1324234734 0.00001
NM_025216.3(WNT10A):c.831G>T (p.Trp277Cys) rs1234227647 0.00001
NM_025216.3(WNT10A):c.959C>G (p.Pro320Arg) rs974508350 0.00001
NM_025216.3(WNT10A):c.1034T>C (p.Phe345Ser) rs1553623335
NM_025216.3(WNT10A):c.1036T>C (p.Cys346Arg)
NM_025216.3(WNT10A):c.1040A>C (p.Glu347Ala)
NM_025216.3(WNT10A):c.1085G>T (p.Cys362Phe) rs1575235098
NM_025216.3(WNT10A):c.1120_1134dup (p.Gly378_Arg379insSerMetCysCysGly)
NM_025216.3(WNT10A):c.1124T>G (p.Met375Arg) rs773598047
NM_025216.3(WNT10A):c.1127G>C (p.Cys376Ser)
NM_025216.3(WNT10A):c.1154G>A (p.Arg385His)
NM_025216.3(WNT10A):c.1199G>C (p.Cys400Ser) rs1575235227
NM_025216.3(WNT10A):c.1204G>A (p.Val402Met)
NM_025216.3(WNT10A):c.1212C>G (p.Cys404Trp) rs1553623396
NM_025216.3(WNT10A):c.1223G>A (p.Arg408His)
NM_025216.3(WNT10A):c.152C>T (p.Pro51Leu)
NM_025216.3(WNT10A):c.275C>T (p.Ala92Val) rs1553622317
NM_025216.3(WNT10A):c.323C>T (p.Ser108Leu) rs2106011706
NM_025216.3(WNT10A):c.364A>T (p.Ile122Phe) rs201929547
NM_025216.3(WNT10A):c.38G>C (p.Arg13Pro)
NM_025216.3(WNT10A):c.434T>C (p.Val145Ala)
NM_025216.3(WNT10A):c.542C>T (p.Ala181Val)
NM_025216.3(WNT10A):c.554G>A (p.Gly185Asp) rs1458852116
NM_025216.3(WNT10A):c.59C>A (p.Pro20Gln)
NM_025216.3(WNT10A):c.623C>T (p.Ser208Phe) rs756543596
NM_025216.3(WNT10A):c.640T>C (p.Cys214Arg)
NM_025216.3(WNT10A):c.667C>T (p.Arg223Cys) rs149245953
NM_025216.3(WNT10A):c.775C>T (p.Arg259Trp)
NM_025216.3(WNT10A):c.791G>T (p.Cys264Phe) rs1944669118
NM_025216.3(WNT10A):c.796G>A (p.Gly266Ser) rs778752861
NM_025216.3(WNT10A):c.914G>T (p.Arg305Leu) rs746769946
NM_025216.3(WNT10A):c.919G>C (p.Gly307Arg)
NM_025216.3(WNT10A):c.987_989dup (p.Arg330dup) rs1416466883

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