Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41583603A>CCA399476558KRT14c.1001T>G (p.Leu334Arg)
n.451T>G
17g.41583603A>GCA399476560KRT14c.1001T>C (p.Leu334Pro)
n.451T>C
17g.41583603A>TCA399476555KRT14c.1001T>A (p.Leu334His)
n.451T>A
17g.41583604G>ACA399476565KRT14c.1000C>T (p.Leu334Phe)
n.450C>T
dbSNP gnomAD v4
17g.41583604G>CCA399476563KRT14c.1000C>G (p.Leu334Val)
n.450C>G
17g.41583604G=CA2260085479KRT14c.1000C= (p.Leu334=)
n.450C=
17g.41583604G>TCA399476567KRT14c.1000C>A (p.Leu334Ile)
n.450C>A
17g.41583605C>ACA399476570KRT14c.999G>T (p.Glu333Asp)
n.449G>T
17g.41583605C=CA2260085480KRT14c.999G= (p.Glu333=)
n.449G=
17g.41583605C>GCA399476572KRT14c.999G>C (p.Glu333Asp)
n.449G>C
17g.41583605C>TCA500205387KRT14c.999G>A (p.Glu333=)
n.449G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.41583606T>ACA399476575KRT14c.998A>T (p.Glu333Val)
n.448A>T
17g.41583606T>CCA399476577KRT14c.998A>G (p.Glu333Gly)
n.448A>G
17g.41583606T>GCA399476579KRT14c.998A>C (p.Glu333Ala)
n.448A>C
17g.41583607C>ACA399476581KRT14c.997G>T (p.Glu333Ter)
n.447G>T
17g.41583607C=CA2260085481KRT14c.997G= (p.Glu333=)
n.447G=
17g.41583607C>GCA399476583KRT14c.997G>C (p.Glu333Gln)
n.447G>C
dbSNP gnomAD v4
17g.41583607C>TCA399476585KRT14c.997G>A (p.Glu333Lys)
n.447G>A
17g.41583608C>ACA500205388KRT14c.996G>T (p.Ser332=)
n.446G>T
17g.41583608C=CA2260085482KRT14c.996G= (p.Ser332=)
n.446G=
17g.41583608C>GCA500205389KRT14c.996G>C (p.Ser332=)
n.446G>C
17g.41583608C>TCA8562543KRT14c.996G>A (p.Ser332=)
n.446G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583609G>ACA8562544KRT14c.995C>T (p.Ser332Leu)
n.445C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41583609G>CCA399476591KRT14c.995C>G (p.Ser332Trp)
n.445C>G
17g.41583609G=CA2260085483KRT14c.995C= (p.Ser332=)
n.445C=
17g.41583609G>TCA399476593KRT14c.995C>A (p.Ser332Ter)
n.445C>A
gnomAD v4
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

Number of alleles fetched