Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.12695626C>ACA372937253TYRP1c.497C>A (p.Ser166Ter)
n.686C>A
dbSNP
9g.12695626C=CA1834018235TYRP1c.497C= (p.Ser166=)
n.686C=
9g.12695626C>GCA127292TYRP1c.497C>G (p.Ser166Ter)
n.686C>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.12695626C>TCA372937255TYRP1c.497C>T (p.Ser166Leu)
n.686C>T
9g.12695627A>CCA464021334TYRP1c.498A>C (p.Ser166=)
n.687A>C
9g.12695627A>GCA464021335TYRP1c.498A>G (p.Ser166=)
n.687A>G
gnomAD v4
9g.12695627A>TCA464021336TYRP1c.498A>T (p.Ser166=)
n.687A>T
9g.12695628G>ACA372937257TYRP1c.499G>A (p.Glu167Lys)
n.688G>A
9g.12695628G>CCA372937258TYRP1c.499G>C (p.Glu167Gln)
n.688G>C
9g.12695628G>TCA372937260TYRP1c.499G>T (p.Glu167Ter)
n.688G>T
9g.12695629A>CCA372937262TYRP1c.500A>C (p.Glu167Ala)
n.689A>C
9g.12695629A>GCA372937264TYRP1c.500A>G (p.Glu167Gly)
n.689A>G
9g.12695629A>TCA372937266TYRP1c.500A>T (p.Glu167Val)
n.689A>T
9g.12695630A>CCA372937268TYRP1c.501A>C (p.Glu167Asp)
n.690A>C
9g.12695630A>GCA464021337TYRP1c.501A>G (p.Glu167=)
n.690A>G
9g.12695630A>TCA372937270TYRP1c.501A>T (p.Glu167Asp)
n.690A>T
9g.12695631G>ACA4985244TYRP1c.502G>A (p.Glu168Lys)
n.691G>A
dbSNP ExAC gnomAD v2
9g.12695631G>CCA372937275TYRP1c.502G>C (p.Glu168Gln)
n.691G>C
9g.12695631G=CA1834018236TYRP1c.502G= (p.Glu168=)
n.691G=
9g.12695631G>TCA372937271TYRP1c.502G>T (p.Glu168Ter)
n.691G>T
9g.12695632A>CCA372937277TYRP1c.503A>C (p.Glu168Ala)
n.692A>C
9g.12695632A>GCA372937279TYRP1c.503A>G (p.Glu168Gly)
n.692A>G
9g.12695632A>TCA372937280TYRP1c.503A>T (p.Glu168Val)
n.692A>T
9g.12695633A>CCA372937283TYRP1c.504A>C (p.Glu168Asp)
n.693A>C
9g.12695633A>GCA464021338TYRP1c.504A>G (p.Glu168=)
n.693A>G
9g.12695633A>TCA372937285TYRP1c.504A>T (p.Glu168Asp)
n.693A>T
9g.12695634A=CA1834018237TYRP1c.505A= (p.Ile169=)
n.694A=
9g.12695634A>CCA372937291TYRP1c.505A>C (p.Ile169Leu)
n.694A>C
9g.12695634A>GCA372937290TYRP1c.505A>G (p.Ile169Val)
n.694A>G
dbSNP gnomAD v3 gnomAD v4
9g.12695634A>TCA372937288TYRP1c.505A>T (p.Ile169Leu)
n.694A>T
9g.12695635T>ACA372937293TYRP1c.506T>A (p.Ile169Lys)
n.695T>A
9g.12695635T>CCA189306322TYRP1c.506T>C (p.Ile169Thr)
n.695T>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.12695635T>GCA372937296TYRP1c.506T>G (p.Ile169Arg)
n.695T>G
9g.12695635T=CA1834018238TYRP1c.506T= (p.Ile169=)
n.695T=
9g.12695636A=CA1834018239TYRP1c.507A= (p.Ile169=)
n.696A=
9g.12695636A>CCA464021340TYRP1c.507A>C (p.Ile169=)
n.696A>C
9g.12695636A>GCA372937298TYRP1c.507A>G (p.Ile169Met)
n.696A>G
9g.12695636A>TCA464021339TYRP1c.507A>T (p.Ile169=)
n.696A>T
dbSNP
9g.12695637C>ACA372937300TYRP1c.508C>A (p.Leu170Met)
n.697C>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.12695637C=CA1834018240TYRP1c.508C= (p.Leu170=)
n.697C=
9g.12695637C>GCA372937302TYRP1c.508C>G (p.Leu170Val)
n.697C>G
9g.12695637C>TCA464021341TYRP1c.508C>T (p.Leu170=)
n.697C>T
gnomAD v4
9g.12695638T>ACA372937308TYRP1c.509T>A (p.Leu170Gln)
n.698T>A
9g.12695638T>CCA372937305TYRP1c.509T>C (p.Leu170Pro)
n.698T>C
9g.12695638T>GCA372937306TYRP1c.509T>G (p.Leu170Arg)
n.698T>G
9g.12695639G>ACA464021342TYRP1c.510G>A (p.Leu170=)
n.699G>A
gnomAD v4
9g.12695639G>CCA464021344TYRP1c.510G>C (p.Leu170=)
n.699G>C
9g.12695639G>TCA464021343TYRP1c.510G>T (p.Leu170=)
n.699G>T
gnomAD v4
9g.12695640G>ACA372937311TYRP1c.511G>A (p.Gly171Arg)
n.700G>A
9g.12695640G>CCA372937312TYRP1c.511G>C (p.Gly171Arg)
n.700G>C

Number of alleles fetched