Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41583610A>CCA399476601KRT14c.994T>G (p.Ser332Ala)
n.444T>G
17g.41583610A>GCA399476598KRT14c.994T>C (p.Ser332Pro)
n.444T>C
17g.41583610A>TCA399476596KRT14c.994T>A (p.Ser332Thr)
n.444T>A
gnomAD v4
17g.41583611G>ACA500205390KRT14c.993C>T (p.Ile331=)
n.443C>T
17g.41583611G>CCA399476603KRT14c.993C>G (p.Ile331Met)
n.443C>G
17g.41583611G=CA2260085484KRT14c.993C= (p.Ile331=)
n.443C=
17g.41583611G>TCA500205391KRT14c.993C>A (p.Ile331=)
n.443C>A
dbSNP gnomAD v2 gnomAD v4
17g.41583612A>CCA399476605KRT14c.992T>G (p.Ile331Ser)
n.442T>G
17g.41583612A>GCA399476607KRT14c.992T>C (p.Ile331Thr)
n.442T>C
17g.41583612A>TCA399476609KRT14c.992T>A (p.Ile331Asn)
n.442T>A
17g.41583613T>ACA399476613KRT14c.991A>T (p.Ile331Phe)
n.441A>T
17g.41583613T>CCA399476615KRT14c.991A>G (p.Ile331Val)
n.441A>G
gnomAD v4
17g.41583613T>GCA8562545KRT14c.991A>C (p.Ile331Leu)
n.441A>C
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41583613T=CA2260085485KRT14c.991A= (p.Ile331=)
n.441A=
17g.41583614C>ACA399476620KRT14c.990G>T (p.Glu330Asp)
n.440G>T
17g.41583614C>GCA399476622KRT14c.990G>C (p.Glu330Asp)
n.440G>C
17g.41583614C>TCA500205392KRT14c.990G>A (p.Glu330=)
n.440G>A
17g.41583615T>ACA399476625KRT14c.989A>T (p.Glu330Val)
n.439A>T
17g.41583615T>CCA399476627KRT14c.989A>G (p.Glu330Gly)
n.439A>G
17g.41583615T>GCA8562546KRT14c.989A>C (p.Glu330Ala)
n.439A>C
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41583615T=CA2260085486KRT14c.989A= (p.Glu330=)
n.439A=
17g.41583616C>ACA399476633KRT14c.988G>T (p.Glu330Ter)
n.438G>T
17g.41583616C=CA2260085487KRT14c.988G= (p.Glu330=)
n.438G=
17g.41583616C>GCA399476630KRT14c.988G>C (p.Glu330Gln)
n.438G>C
17g.41583616C>TCA8562547KRT14c.988G>A (p.Glu330Lys)
n.438G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583617G>ACA8562548KRT14c.987C>T (p.Ser329=)
n.437C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583617G>CCA399476639KRT14c.987C>G (p.Ser329Arg)
n.437C>G
gnomAD v4
17g.41583617G=CA2260085488KRT14c.987C= (p.Ser329=)
n.437C=
17g.41583617G>TCA399476636KRT14c.987C>A (p.Ser329Arg)
n.437C>A
dbSNP gnomAD v4
17g.41583618C>ACA399476641KRT14c.986G>T (p.Ser329Ile)
n.436G>T
17g.41583618C=CA2260085489KRT14c.986G= (p.Ser329=)
n.436G=
17g.41583618C>GCA399476642KRT14c.986G>C (p.Ser329Thr)
n.436G>C
gnomAD v4
17g.41583618C>TCA399476644KRT14c.986G>A (p.Ser329Asn)
n.436G>A
dbSNP
17g.41583619T>ACA399476647KRT14c.985A>T (p.Ser329Cys)
n.435A>T
17g.41583619T>CCA399476649KRT14c.985A>G (p.Ser329Gly)
n.435A>G
gnomAD v4
17g.41583619T>GCA399476651KRT14c.985A>C (p.Ser329Arg)
n.435A>C
17g.41583620C>ACA399476652KRT14c.984G>T (p.Lys328Asn)
n.434G>T
17g.41583620C>GCA399476654KRT14c.984G>C (p.Lys328Asn)
n.434G>C
17g.41583620C>TCA500205393KRT14c.984G>A (p.Lys328=)
n.434G>A
ClinVar
17g.41583621T>ACA399476659KRT14c.983A>T (p.Lys328Met)
n.433A>T
17g.41583621T>CCA399476660KRT14c.983A>G (p.Lys328Arg)
n.433A>G
17g.41583621T>GCA399476663KRT14c.983A>C (p.Lys328Thr)
n.433A>C
17g.41583622T>ACA399476671KRT14c.982A>T (p.Lys328Ter)
n.432A>T
17g.41583622T>CCA399476669KRT14c.982A>G (p.Lys328Glu)
n.432A>G
17g.41583622T>GCA399476667KRT14c.982A>C (p.Lys328Gln)
n.432A>C
17g.41583623G>ACA500205394KRT14c.981C>T (p.Gly327=)
n.431C>T
17g.41583623G>CCA500205395KRT14c.981C>G (p.Gly327=)
n.431C>G
gnomAD v4
17g.41583623G>TCA500205396KRT14c.981C>A (p.Gly327=)
n.431C>A
17g.41583624C>ACA399476673KRT14c.980G>T (p.Gly327Val)
n.430G>T
17g.41583624C>GCA399476675KRT14c.980G>C (p.Gly327Ala)
n.430G>C

Number of alleles fetched