Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.52813934C>ACA384991216KRT4c.125G>T (p.Cys42Phe)
COSMIC
12g.52813934C>GCA384991217KRT4c.125G>C (p.Cys42Ser)
12g.52813934C>TCA384991218KRT4c.125G>A (p.Cys42Tyr)
12g.52813935A>CCA384991219KRT4c.124T>G (p.Cys42Gly)
12g.52813935A>GCA384991221KRT4c.124T>C (p.Cys42Arg)
gnomAD v4
12g.52813935A>TCA384991220KRT4c.124T>A (p.Cys42Ser)
ClinVar
12g.52813936T>ACA480076156KRT4c.123A>T (p.Arg41=)
12g.52813936T>CCA480076157KRT4c.123A>G (p.Arg41=)
12g.52813936T>GCA480076158KRT4c.123A>C (p.Arg41=)
12g.52813937C>ACA384991222KRT4c.122G>T (p.Arg41Leu)
12g.52813937C=CA2036663514KRT4c.122G= (p.Arg41=)
12g.52813937C>GCA384991223KRT4c.122G>C (p.Arg41Pro)
12g.52813937C>TCA6588836KRT4c.122G>A (p.Arg41Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52813938G>ACA6588837KRT4c.121C>T (p.Arg41Ter)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52813938G>CCA384991224KRT4c.121C>G (p.Arg41Gly)
12g.52813938G=CA2036663515KRT4c.121C= (p.Arg41=)
12g.52813938G>TCA480076159KRT4c.121C>A (p.Arg41=)
12g.52813939G>ACA480076162KRT4c.120C>T (p.Gly40=)
12g.52813939G>CCA480076161KRT4c.120C>G (p.Gly40=)
12g.52813939G>TCA480076160KRT4c.120C>A (p.Gly40=)
12g.52813940C>ACA384991225KRT4c.119G>T (p.Gly40Val)
12g.52813940C=CA2036663516KRT4c.119G= (p.Gly40=)
12g.52813940C>GCA384991226KRT4c.119G>C (p.Gly40Ala)
12g.52813940C>TCA6588838KRT4c.119G>A (p.Gly40Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52813941C>ACA384991227KRT4c.118G>T (p.Gly40Cys)
12g.52813941C>GCA384991229KRT4c.118G>C (p.Gly40Arg)
12g.52813941C>TCA384991228KRT4c.118G>A (p.Gly40Ser)
12g.52813942A>CCA480076165KRT4c.117T>G (p.Ala39=)
gnomAD v4
12g.52813942A>GCA480076164KRT4c.117T>C (p.Ala39=)
12g.52813942A>TCA480076163KRT4c.117T>A (p.Ala39=)
12g.52813943G>ACA384991230KRT4c.116C>T (p.Ala39Val)
dbSNP gnomAD v2 gnomAD v4
12g.52813943G>CCA384991232KRT4c.116C>G (p.Ala39Gly)
12g.52813943G=CA2036663517KRT4c.116C= (p.Ala39=)
12g.52813943G>TCA384991231KRT4c.116C>A (p.Ala39Asp)
dbSNP gnomAD v2 gnomAD v4
12g.52813944delCA2618967542KRT4c.115del (p.Ala39LeufsTer25)
gnomAD v4
12g.52813944C>ACA6588840KRT4c.115G>T (p.Ala39Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52813944C=CA2036663518KRT4c.115G= (p.Ala39=)
12g.52813944C>GCA384991233KRT4c.115G>C (p.Ala39Pro)
12g.52813944C>TCA6588839KRT4c.115G>A (p.Ala39Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52813945A>CCA480076166KRT4c.114T>G (p.Gly38=)
12g.52813945A>GCA480076168KRT4c.114T>C (p.Gly38=)
12g.52813945A>TCA480076167KRT4c.114T>A (p.Gly38=)
12g.52813946C>ACA384991234KRT4c.113G>T (p.Gly38Val)
12g.52813946C>GCA384991235KRT4c.113G>C (p.Gly38Ala)
12g.52813946C>TCA384991236KRT4c.113G>A (p.Gly38Asp)
12g.52813947C>ACA384991237KRT4c.112G>T (p.Gly38Cys)
12g.52813947C=CA2036663519KRT4c.112G= (p.Gly38=)
12g.52813947C>GCA384991238KRT4c.112G>C (p.Gly38Arg)
12g.52813947C>TCA384991239KRT4c.112G>A (p.Gly38Ser)
dbSNP gnomAD v2 gnomAD v4
12g.52813948T>ACA480076169KRT4c.111A>T (p.Gly37=)

Number of alleles fetched