Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.52447821C>ACA384981909KRT6Bc.1381G>T (p.Glu461Ter)
12g.52447821C=CA2036494081KRT6Bc.1381G= (p.Glu461=)
12g.52447821C>GCA384981912KRT6Bc.1381G>C (p.Glu461Gln)
12g.52447821C>TCA217366KRT6Bc.1381G>A (p.Glu461Lys)
ClinVar dbSNP COSMIC
12g.52447822C>ACA480068900KRT6Bc.1380G>T (p.Val460=)
12g.52447822C>GCA480068901KRT6Bc.1380G>C (p.Val460=)
gnomAD v4
12g.52447822C>TCA480068899KRT6Bc.1380G>A (p.Val460=)
12g.52447823A>CCA384981916KRT6Bc.1379T>G (p.Val460Gly)
12g.52447823A>GCA384981919KRT6Bc.1379T>C (p.Val460Ala)
12g.52447823A>TCA384981922KRT6Bc.1379T>A (p.Val460Glu)
12g.52447824C>ACA384981926KRT6Bc.1378G>T (p.Val460Leu)
12g.52447824C>GCA384981928KRT6Bc.1378G>C (p.Val460Leu)
12g.52447824C>TCA384981930KRT6Bc.1378G>A (p.Val460Met)
gnomAD v4
12g.52447825A=CA2036494090KRT6Bc.1377T= (p.Asp459=)
12g.52447825A>CCA384981937KRT6Bc.1377T>G (p.Asp459Glu)
12g.52447825A>GCA6580432KRT6Bc.1377T>C (p.Asp459=)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52447825A>TCA384981935KRT6Bc.1377T>A (p.Asp459Glu)
12g.52447826T>ACA384981940KRT6Bc.1376A>T (p.Asp459Val)
12g.52447826T>CCA384981942KRT6Bc.1376A>G (p.Asp459Gly)
gnomAD v4
12g.52447826T>GCA384981944KRT6Bc.1376A>C (p.Asp459Ala)
12g.52447827C>ACA384981946KRT6Bc.1375G>T (p.Asp459Tyr)
12g.52447827C>GCA384981948KRT6Bc.1375G>C (p.Asp459His)
12g.52447827C>TCA384981950KRT6Bc.1375G>A (p.Asp459Asn)
12g.52447828C>ACA480068906KRT6Bc.1374G>T (p.Leu458=)
12g.52447828C=CA2036494112KRT6Bc.1374G= (p.Leu458=)
12g.52447828C>GCA480068905KRT6Bc.1374G>C (p.Leu458=)
12g.52447828C>TCA6580433KRT6Bc.1374G>A (p.Leu458=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52447829A>CCA384981954KRT6Bc.1373T>G (p.Leu458Arg)
12g.52447829A>GCA384981956KRT6Bc.1373T>C (p.Leu458Pro)
gnomAD v4
12g.52447829A>TCA384981960KRT6Bc.1373T>A (p.Leu458Gln)
12g.52447830G>ACA480068907KRT6Bc.1372C>T (p.Leu458=)
dbSNP gnomAD v2 gnomAD v4
12g.52447830G>CCA384981963KRT6Bc.1372C>G (p.Leu458Val)
12g.52447830G=CA2036494115KRT6Bc.1372C= (p.Leu458=)
12g.52447830G>TCA384981965KRT6Bc.1372C>A (p.Leu458Met)
12g.52447831G>ACA480068908KRT6Bc.1371C>T (p.Ala457=)
12g.52447831G>CCA480068909KRT6Bc.1371C>G (p.Ala457=)
12g.52447831G=CA2036494117KRT6Bc.1371C= (p.Ala457=)
12g.52447831G>TCA6580434KRT6Bc.1371C>A (p.Ala457=)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52447832G>ACA384981976KRT6Bc.1370C>T (p.Ala457Val)
12g.52447832G>CCA384981973KRT6Bc.1370C>G (p.Ala457Gly)
dbSNP gnomAD v4
12g.52447832G=CA2036494120KRT6Bc.1370C= (p.Ala457=)
12g.52447832G>TCA384981971KRT6Bc.1370C>A (p.Ala457Asp)
12g.52447833C>ACA384981979KRT6Bc.1369G>T (p.Ala457Ser)
12g.52447833C=CA2036494124KRT6Bc.1369G= (p.Ala457=)
12g.52447833C>GCA384981981KRT6Bc.1369G>C (p.Ala457Pro)
dbSNP gnomAD v2 gnomAD v4
12g.52447833C>TCA384981982KRT6Bc.1369G>A (p.Ala457Thr)
gnomAD v4
12g.52447834C>ACA480068912KRT6Bc.1368G>T (p.Leu456=)
12g.52447834C>GCA480068910KRT6Bc.1368G>C (p.Leu456=)
12g.52447834C>TCA480068911KRT6Bc.1368G>A (p.Leu456=)
12g.52447835A>CCA384981985KRT6Bc.1367T>G (p.Leu456Arg)

Number of alleles fetched