Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.52676334C>ACA6586173KRT1c.1416G>T (p.Lys472Asn)
n.490G>T
dbSNP ExAC gnomAD v2
12g.52676334C=CA2036619581KRT1c.1416G= (p.Lys472=)
n.490G=
12g.52676334C>GCA384962366KRT1c.1416G>C (p.Lys472Asn)
n.490G>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.52676334C>TCA479872170KRT1c.1416G>A (p.Lys472=)
n.490G>A
dbSNP gnomAD v2 gnomAD v4
12g.52676335T>ACA384962369KRT1c.1415A>T (p.Lys472Met)
n.489A>T
12g.52676335T>CCA384962372KRT1c.1415A>G (p.Lys472Arg)
n.489A>G
gnomAD v4
12g.52676335T>GCA384962370KRT1c.1415A>C (p.Lys472Thr)
n.489A>C
12g.52676336T>ACA384962374KRT1c.1414A>T (p.Lys472Ter)
n.488A>T
12g.52676336T>CCA384962376KRT1c.1414A>G (p.Lys472Glu)
n.488A>G
12g.52676336T>GCA384962377KRT1c.1414A>C (p.Lys472Gln)
n.488A>C
12g.52676337T>ACA479873082KRT1c.1413A>T (p.Thr471=)
n.487A>T
dbSNP
12g.52676337T>CCA479873084KRT1c.1413A>G (p.Thr471=)
n.487A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.52676337T>GCA6586174KRT1c.1413A>C (p.Thr471=)
n.487A>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52676337T=CA217417KRT1c.1413A= (p.Thr471=)
n.487A=
12g.52676338G>ACA384962383KRT1c.1412C>T (p.Thr471Ile)
n.486C>T
12g.52676338G>CCA384962385KRT1c.1412C>G (p.Thr471Arg)
n.486C>G
c.1412C>G (p.Thr471Ser)
12g.52676338G>TCA384962386KRT1c.1412C>A (p.Thr471Lys)
n.486C>A
c.1412C>A (p.Thr471Asn)
12g.52676339T>ACA384962389KRT1c.1411A>T (p.Thr471Ser)
n.485A>T
12g.52676339T>CCA384962391KRT1c.1411A>G (p.Thr471Ala)
n.485A>G
12g.52676339T>GCA384962393KRT1c.1411A>C (p.Thr471Pro)
n.485A>C
12g.52676340G>ACA479873111KRT1c.1410C>T (p.Asn470=)
n.484C>T
dbSNP gnomAD v4
12g.52676340G>CCA384962396KRT1c.1410C>G (p.Asn470Lys)
n.484C>G
12g.52676340G=CA2036619582KRT1c.1410C= (p.Asn470=)
n.484C=
12g.52676340G>TCA384962395KRT1c.1410C>A (p.Asn470Lys)
n.484C>A
12g.52676341T>ACA384962398KRT1c.1409A>T (p.Asn470Ile)
n.483A>T
12g.52676341T>CCA384962399KRT1c.1409A>G (p.Asn470Ser)
n.483A>G
12g.52676341T>GCA384962400KRT1c.1409A>C (p.Asn470Thr)
n.483A>C
12g.52676342T>ACA384962402KRT1c.1408A>T (p.Asn470Tyr)
n.482A>T
12g.52676342T>CCA6586175KRT1c.1408A>G (p.Asn470Asp)
n.482A>G
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52676342T>GCA384962405KRT1c.1408A>C (p.Asn470His)
n.482A>C
COSMIC
12g.52676342T=CA2036619583KRT1c.1408A= (p.Asn470=)
n.482A=
12g.52676343C>ACA384962408KRT1c.1407G>T (p.Met469Ile)
n.481G>T
12g.52676343C>GCA384962409KRT1c.1407G>C (p.Met469Ile)
n.481G>C
12g.52676343C>TCA384962411KRT1c.1407G>A (p.Met469Ile)
n.481G>A
12g.52676344A=CA2036619584KRT1c.1406T= (p.Met469=)
n.480T=
12g.52676344A>CCA384962414KRT1c.1406T>G (p.Met469Arg)
n.480T>G
gnomAD v4
12g.52676344A>GCA6586176KRT1c.1406T>C (p.Met469Thr)
n.480T>C
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52676344A>TCA384962416KRT1c.1406T>A (p.Met469Lys)
n.480T>A
gnomAD v4
12g.52676345T>ACA384962422KRT1c.1405A>T (p.Met469Leu)
n.479A>T
12g.52676345T>CCA384962424KRT1c.1405A>G (p.Met469Val)
n.479A>G
12g.52676345T>GCA384962420KRT1c.1405A>C (p.Met469Leu)
n.479A>C
12g.52676346C>ACA479873156KRT1c.1404G>T (p.Leu468=)
n.478G>T
12g.52676346C>GCA479873152KRT1c.1404G>C (p.Leu468=)
n.478G>C
12g.52676346C>TCA479873148KRT1c.1404G>A (p.Leu468=)
n.478G>A
12g.52676347A>CCA384962434KRT1c.1403T>G (p.Leu468Arg)
n.477T>G
12g.52676347A>GCA384962429KRT1c.1403T>C (p.Leu468Pro)
n.477T>C
gnomAD v4
12g.52676347A>TCA384962431KRT1c.1403T>A (p.Leu468Gln)
n.477T>A
12g.52676348G>ACA479873160KRT1c.1402C>T (p.Leu468=)
n.476C>T
dbSNP gnomAD v4
12g.52676348G>CCA384962437KRT1c.1402C>G (p.Leu468Val)
n.476C>G
12g.52676348G=CA2036619585KRT1c.1402C= (p.Leu468=)
n.476C=
12g.52676348G>TCA384962440KRT1c.1402C>A (p.Leu468Met)
n.476C>A
gnomAD v4
12g.52676349C>ACA384962442KRT1c.1401G>T (p.Glu467Asp)
n.475G>T
12g.52676349C>GCA384962444KRT1c.1401G>C (p.Glu467Asp)
n.475G>C
12g.52676349C>TCA479873170KRT1c.1401G>A (p.Glu467=)
n.475G>A
gnomAD v4
12g.52676350T>ACA384962448KRT1c.1400A>T (p.Glu467Val)
n.474A>T
12g.52676350T>CCA384962450KRT1c.1400A>G (p.Glu467Gly)
n.474A>G
12g.52676350T>GCA384962453KRT1c.1400A>C (p.Glu467Ala)
n.474A>C
12g.52676350_52676374delinsTCCTGGTAGTCGCGCAGCAGGCGGGCA2036619586KRT1c.1376_1400delinsCCCGCCTGCTGCGCGACTACCAGGA (p.Ala459=)
n.450_474delinsCCCGCCTGCTGCGCGACTACCAGGA
12g.52676351C>ACA384962458KRT1c.1399G>T (p.Glu467Ter)
n.473G>T
gnomAD v4
12g.52676351C=CA2036619587KRT1c.1399G= (p.Glu467=)
n.473G=
12g.52676351C>GCA6586177KRT1c.1399G>C (p.Glu467Gln)
n.473G>C
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52676351C>TCA384962463KRT1c.1399G>A (p.Glu467Lys)
n.473G>A
gnomAD v4
12g.52676353_52676376delCA217413KRT1c.1376_1399del (p.Ala459_Gln466del)
n.450_473del
ClinVar dbSNP
12g.52676352C>ACA384962466KRT1c.1398G>T (p.Gln466His)
n.472G>T
12g.52676352C>GCA384962469KRT1c.1398G>C (p.Gln466His)
n.472G>C
12g.52676352C>TCA479873192KRT1c.1398G>A (p.Gln466=)
n.472G>A
12g.52676353T>ACA384962470KRT1c.1397A>T (p.Gln466Leu)
n.471A>T
12g.52676353T>CCA6586178KRT1c.1397A>G (p.Gln466Arg)
n.471A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52676353T>GCA384962471KRT1c.1397A>C (p.Gln466Pro)
n.471A>C
12g.52676353T=CA2036619588KRT1c.1397A= (p.Gln466=)
n.471A=
12g.52676354G>ACA384962472KRT1c.1396C>T (p.Gln466Ter)
n.470C>T
12g.52676354G>CCA384962474KRT1c.1396C>G (p.Gln466Glu)
n.470C>G
12g.52676354G>TCA384962476KRT1c.1396C>A (p.Gln466Lys)
n.470C>A
12g.52676355G>ACA479873219KRT1c.1395C>T (p.Tyr465=)
n.469C>T
12g.52676355G>CCA384962478KRT1c.1395C>G (p.Tyr465Ter)
n.469C>G
12g.52676355G>TCA384962481KRT1c.1395C>A (p.Tyr465Ter)
n.469C>A
COSMIC
12g.52676356T>ACA384962484KRT1c.1394A>T (p.Tyr465Phe)
n.468A>T
12g.52676356T>CCA384962486KRT1c.1394A>G (p.Tyr465Cys)
n.468A>G
dbSNP gnomAD v2 gnomAD v4 COSMIC
12g.52676356T>GCA384962489KRT1c.1394A>C (p.Tyr465Ser)
n.468A>C
12g.52676356T=CA2036619589KRT1c.1394A= (p.Tyr465=)
n.468A=
12g.52676357A=CA2036619590KRT1c.1393T= (p.Tyr465=)
n.467T=
12g.52676357A>CCA384962495KRT1c.1393T>G (p.Tyr465Asp)
n.467T>G
dbSNP gnomAD v2 gnomAD v4
12g.52676357A>GCA384962497KRT1c.1393T>C (p.Tyr465His)
n.467T>C
12g.52676357A>TCA384962493KRT1c.1393T>A (p.Tyr465Asn)
n.467T>A
12g.52676358G>ACA479873243KRT1c.1392C>T (p.Asp464=)
n.466C>T
12g.52676358G>CCA384962501KRT1c.1392C>G (p.Asp464Glu)
n.466C>G
12g.52676358G>TCA384962503KRT1c.1392C>A (p.Asp464Glu)
n.466C>A
12g.52676359T>ACA384962507KRT1c.1391A>T (p.Asp464Val)
n.465A>T
12g.52676359T>CCA384962510KRT1c.1391A>G (p.Asp464Gly)
n.465A>G
12g.52676359T>GCA384962513KRT1c.1391A>C (p.Asp464Ala)
n.465A>C
12g.52676360C>ACA384962516KRT1c.1390G>T (p.Asp464Tyr)
n.464G>T
12g.52676360C=CA2036619591KRT1c.1390G= (p.Asp464=)
n.464G=
12g.52676360C>GCA384962519KRT1c.1390G>C (p.Asp464His)
n.464G>C
12g.52676360C>TCA6586179KRT1c.1390G>A (p.Asp464Asn)
n.464G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.52676361G>ACA217415KRT1c.1389C>T (p.Arg463=)
n.463C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52676361G>CCA237262386KRT1c.1389C>G (p.Arg463=)
n.463C>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.52676361G=CA2036619592KRT1c.1389C= (p.Arg463=)
n.463C=
12g.52676361G>TCA479873274KRT1c.1389C>A (p.Arg463=)
n.463C>A
gnomAD v4
12g.52676362C>ACA384962525KRT1c.1388G>T (p.Arg463Leu)
n.462G>T
12g.52676362C=CA2036619593KRT1c.1388G= (p.Arg463=)
n.462G=
12g.52676362C>GCA384962528KRT1c.1388G>C (p.Arg463Pro)
n.462G>C
12g.52676362C>TCA6586180KRT1c.1388G>A (p.Arg463His)
n.462G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52676363G>ACA6586181KRT1c.1387C>T (p.Arg463Cys)
n.461C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.52676363G>CCA384962536KRT1c.1387C>G (p.Arg463Gly)
n.461C>G
gnomAD v3 gnomAD v4
12g.52676363G=CA2036619594KRT1c.1387C= (p.Arg463=)
n.461C=
12g.52676363G>TCA384962532KRT1c.1387C>A (p.Arg463Ser)
n.461C>A
gnomAD v4
12g.52676364C>ACA479873296KRT1c.1386G>T (p.Leu462=)
n.460G>T
12g.52676364C>GCA479873299KRT1c.1386G>C (p.Leu462=)
n.460G>C
12g.52676364C>TCA479873301KRT1c.1386G>A (p.Leu462=)
n.460G>A
12g.52676365A=CA2036619595KRT1c.1385T= (p.Leu462=)
n.459T=
12g.52676365A>CCA384962540KRT1c.1385T>G (p.Leu462Arg)
n.459T>G
12g.52676365A>GCA384962542KRT1c.1385T>C (p.Leu462Pro)
n.459T>C
12g.52676365A>TCA384962545KRT1c.1385T>A (p.Leu462Gln)
n.459T>A
dbSNP
12g.52676366G>ACA479873314KRT1c.1384C>T (p.Leu462=)
n.458C>T
12g.52676366G>CCA384962548KRT1c.1384C>G (p.Leu462Val)
n.458C>G
12g.52676366G>TCA384962551KRT1c.1384C>A (p.Leu462Met)
n.458C>A
12g.52676367C>ACA479873326KRT1c.1383G>T (p.Leu461=)
n.457G>T
12g.52676367C>GCA479873324KRT1c.1383G>C (p.Leu461=)
n.457G>C
12g.52676367C>TCA479873321KRT1c.1383G>A (p.Leu461=)
n.457G>A
12g.52676368A>CCA384962562KRT1c.1382T>G (p.Leu461Arg)
n.456T>G
12g.52676368A>GCA384962555KRT1c.1382T>C (p.Leu461Pro)
n.456T>C
12g.52676368A>TCA384962559KRT1c.1382T>A (p.Leu461Gln)
n.456T>A
12g.52676369G>ACA6586182KRT1c.1381C>T (p.Leu461=)
n.455C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52676369G>CCA384962566KRT1c.1381C>G (p.Leu461Val)
n.455C>G
12g.52676369G=CA2036619596KRT1c.1381C= (p.Leu461=)
n.455C=
12g.52676369G>TCA384962569KRT1c.1381C>A (p.Leu461Met)
n.455C>A
12g.52676370G>ACA479873347KRT1c.1380C>T (p.Arg460=)
n.454C>T
dbSNP
12g.52676370G>CCA479873350KRT1c.1380C>G (p.Arg460=)
n.454C>G
12g.52676370G=CA2036619597KRT1c.1380C= (p.Arg460=)
n.454C=
12g.52676370G>TCA479873353KRT1c.1380C>A (p.Arg460=)
n.454C>A
12g.52676371C>ACA6586183KRT1c.1379G>T (p.Arg460Leu)
n.453G>T
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52676371C=CA2036619598KRT1c.1379G= (p.Arg460=)
n.453G=
12g.52676371C>GCA384962570KRT1c.1379G>C (p.Arg460Pro)
n.453G>C
12g.52676371C>TCA237262424KRT1c.1379G>A (p.Arg460His)
n.453G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.52676372G>ACA6586184KRT1c.1378C>T (p.Arg460Cys)
n.452C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52676372G>CCA6586185KRT1c.1378C>G (p.Arg460Gly)
n.452C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52676372G=CA2036619599KRT1c.1378C= (p.Arg460=)
n.452C=
12g.52676372G>TCA384962573KRT1c.1378C>A (p.Arg460Ser)
n.452C>A
COSMIC
12g.52676373G>ACA479873375KRT1c.1377C>T (p.Ala459=)
n.451C>T
12g.52676373G>CCA479873383KRT1c.1377C>G (p.Ala459=)
n.451C>G
12g.52676373G>TCA479873379KRT1c.1377C>A (p.Ala459=)
n.451C>A
12g.52676374G>ACA237262449KRT1c.1376C>T (p.Ala459Val)
n.450C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.52676374G>CCA6586186KRT1c.1376C>G (p.Ala459Gly)
n.450C>G
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52676374G=CA2036619600KRT1c.1376C= (p.Ala459=)
n.450C=
12g.52676374G>TCA384962586KRT1c.1376C>A (p.Ala459Asp)
n.450C>A
12g.52676375C>ACA384962592KRT1c.1375G>T (p.Ala459Ser)
n.449G>T
12g.52676375C=CA2036619601KRT1c.1375G= (p.Ala459=)
n.449G=
12g.52676375C>GCA384962594KRT1c.1375G>C (p.Ala459Pro)
n.449G>C
dbSNP
12g.52676375C>TCA384962596KRT1c.1375G>A (p.Ala459Thr)
n.449G>A
12g.52676376C>ACA479873395KRT1c.1374G>T (p.Leu458=)
n.448G>T
12g.52676376C>GCA479873398KRT1c.1374G>C (p.Leu458=)
n.448G>C
12g.52676376C>TCA479873402KRT1c.1374G>A (p.Leu458=)
n.448G>A
12g.52676377A>CCA384962598KRT1c.1373T>G (p.Leu458Arg)
n.447T>G
12g.52676377A>GCA384962603KRT1c.1373T>C (p.Leu458Pro)
n.447T>C
12g.52676377A>TCA384962599KRT1c.1373T>A (p.Leu458Gln)
n.447T>A
12g.52676378G>ACA479873413KRT1c.1372C>T (p.Leu458=)
n.446C>T
12g.52676378G>CCA384962605KRT1c.1372C>G (p.Leu458Val)
n.446C>G
12g.52676378G>TCA384962606KRT1c.1372C>A (p.Leu458Met)
n.446C>A
12g.52676379G>ACA479873422KRT1c.1371C>T (p.Asp457=)
n.445C>T
dbSNP gnomAD v4
12g.52676379G>CCA384962610KRT1c.1371C>G (p.Asp457Glu)
n.445C>G
12g.52676379G=CA2036619602KRT1c.1371C= (p.Asp457=)
n.445C=
12g.52676379G>TCA384962612KRT1c.1371C>A (p.Asp457Glu)
n.445C>A
12g.52676380T>ACA384962619KRT1c.1370A>T (p.Asp457Val)
n.444A>T
12g.52676380T>CCA384962614KRT1c.1370A>G (p.Asp457Gly)
n.444A>G
12g.52676380T>GCA384962617KRT1c.1370A>C (p.Asp457Ala)
n.444A>C
dbSNP
12g.52676380T=CA2036619603KRT1c.1370A= (p.Asp457=)
n.444A=
12g.52676381C>ACA6586187KRT1c.1369G>T (p.Asp457Tyr)
n.443G>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52676381C=CA2036619604KRT1c.1369G= (p.Asp457=)
n.443G=
12g.52676381C>GCA384962624KRT1c.1369G>C (p.Asp457His)
n.443G>C
12g.52676381C>TCA384962626KRT1c.1369G>A (p.Asp457Asn)
n.443G>A
gnomAD v4 COSMIC
12g.52676382T>ACA384962629KRT1c.1368A>T (p.Glu456Asp)
n.442A>T
dbSNP
12g.52676382T>CCA479873447KRT1c.1368A>G (p.Glu456=)
n.442A>G
12g.52676382T>GCA384962632KRT1c.1368A>C (p.Glu456Asp)
n.442A>C
12g.52676382T=CA2036619605KRT1c.1368A= (p.Glu456=)
n.442A=
12g.52676383T>ACA384962635KRT1c.1367A>T (p.Glu456Val)
n.441A>T
12g.52676383T>CCA384962637KRT1c.1367A>G (p.Glu456Gly)
n.441A>G
dbSNP gnomAD v4
12g.52676383T>GCA384962641KRT1c.1367A>C (p.Glu456Ala)
n.441A>C
12g.52676383T=CA2036619606KRT1c.1367A= (p.Glu456=)
n.441A=
12g.52676384C>ACA384962644KRT1c.1366G>T (p.Glu456Ter)
n.440G>T
12g.52676384C>GCA384962646KRT1c.1366G>C (p.Glu456Gln)
n.440G>C
12g.52676384C>TCA384962653KRT1c.1366G>A (p.Glu456Lys)
n.440G>A
12g.52676385C>ACA384962656KRT1c.1365G>T (p.Lys455Asn)
n.439G>T
COSMIC
12g.52676385C>GCA384962659KRT1c.1365G>C (p.Lys455Asn)
n.439G>C
12g.52676385C>TCA479873472KRT1c.1365G>A (p.Lys455=)
n.439G>A
gnomAD v4 COSMIC
12g.52676386T>ACA384962677KRT1c.1364A>T (p.Lys455Met)
n.438A>T
12g.52676386T>CCA384962662KRT1c.1364A>G (p.Lys455Arg)
n.438A>G
dbSNP gnomAD v3 gnomAD v4
12g.52676386T>GCA384962674KRT1c.1364A>C (p.Lys455Thr)
n.438A>C
12g.52676386T=CA2036619607KRT1c.1364A= (p.Lys455=)
n.438A=
12g.52676387T>ACA384962679KRT1c.1363A>T (p.Lys455Ter)
n.437A>T
12g.52676387T>CCA384962680KRT1c.1363A>G (p.Lys455Glu)
n.437A>G
12g.52676387T>GCA384962684KRT1c.1363A>C (p.Lys455Gln)
n.437A>C
12g.52676388G>ACA6586188KRT1c.1362C>T (p.Ala454=)
n.436C>T
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52676388G>CCA479873487KRT1c.1362C>G (p.Ala454=)
n.436C>G
12g.52676388G=CA2036619608KRT1c.1362C= (p.Ala454=)
n.436C=
12g.52676388G>TCA479873489KRT1c.1362C>A (p.Ala454=)
n.436C>A
12g.52676389G>ACA384962695KRT1c.1361C>T (p.Ala454Val)
n.435C>T
dbSNP gnomAD v2 gnomAD v4
12g.52676389G>CCA384962700KRT1c.1361C>G (p.Ala454Gly)
n.435C>G
12g.52676389G=CA2036619609KRT1c.1361C= (p.Ala454=)
n.435C=
12g.52676389G>TCA384962702KRT1c.1361C>A (p.Ala454Asp)
n.435C>A
gnomAD v4
12g.52676390C>ACA217411KRT1c.1360G>T (p.Ala454Ser)
n.434G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52676390C=CA2036619610KRT1c.1360G= (p.Ala454=)
n.434G=
12g.52676390C>GCA384962705KRT1c.1360G>C (p.Ala454Pro)
n.434G>C
dbSNP
12g.52676390C>TCA384962708KRT1c.1360G>A (p.Ala454Thr)
n.434G>A
dbSNP gnomAD v2
12g.52676391C>ACA384962715KRT1c.1359G>T (p.Gln453His)
n.433G>T
12g.52676391C>GCA384962718KRT1c.1359G>C (p.Gln453His)
n.433G>C
12g.52676391C>TCA479873510KRT1c.1359G>A (p.Gln453=)
n.433G>A
gnomAD v4
12g.52676392T>ACA384962722KRT1c.1358A>T (p.Gln453Leu)
n.432A>T
dbSNP
12g.52676392T>CCA384962731KRT1c.1358A>G (p.Gln453Arg)
n.432A>G
12g.52676392T>GCA384962733KRT1c.1358A>C (p.Gln453Pro)
n.432A>C
ClinVar dbSNP
12g.52676392T=CA2036619611KRT1c.1358A= (p.Gln453=)
n.432A=
12g.52676393G>ACA384962735KRT1c.1357C>T (p.Gln453Ter)
n.431C>T
12g.52676393G>CCA384962749KRT1c.1357C>G (p.Gln453Glu)
n.431C>G
12g.52676393G>TCA384962737KRT1c.1357C>A (p.Gln453Lys)
n.431C>A
12g.52676394C>ACA384962762KRT1c.1356G>T (p.Gln452His)
n.430G>T
12g.52676394C>GCA384962766KRT1c.1356G>C (p.Gln452His)
n.430G>C
12g.52676394C>TCA479873530KRT1c.1356G>A (p.Gln452=)
n.430G>A
12g.52676395T>ACA384962771KRT1c.1355A>T (p.Gln452Leu)
n.429A>T
gnomAD v4
12g.52676395T>CCA384962775KRT1c.1355A>G (p.Gln452Arg)
n.429A>G
12g.52676395T>GCA384962780KRT1c.1355A>C (p.Gln452Pro)
n.429A>C
12g.52676396G>ACA384962787KRT1c.1354C>T (p.Gln452Ter)
n.428C>T
12g.52676396G>CCA384962789KRT1c.1354C>G (p.Gln452Glu)
n.428C>G
12g.52676396G>TCA384962795KRT1c.1354C>A (p.Gln452Lys)
n.428C>A
gnomAD v4
12g.52676397C>ACA479873547KRT1c.1353G>T (p.Leu451=)
n.427G>T
12g.52676397C>GCA479873549KRT1c.1353G>C (p.Leu451=)
n.427G>C
12g.52676397C>TCA479873553KRT1c.1353G>A (p.Leu451=)
n.427G>A
12g.52676398A=CA2036619612KRT1c.1352T= (p.Leu451=)
n.426T=
12g.52676398A>CCA384962798KRT1c.1352T>G (p.Leu451Arg)
n.426T>G
12g.52676398A>GCA384962799KRT1c.1352T>C (p.Leu451Pro)
n.426T>C
dbSNP gnomAD v4
12g.52676398A>TCA384962802KRT1c.1352T>A (p.Leu451Gln)
n.426T>A
12g.52676399G>ACA6586189KRT1c.1351C>T (p.Leu451=)
n.425C>T
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52676399G>CCA384962827KRT1c.1351C>G (p.Leu451Val)
n.425C>G
dbSNP gnomAD v4
12g.52676399G=CA2036619613KRT1c.1351C= (p.Leu451=)
n.425C=
12g.52676399G>TCA384962822KRT1c.1351C>A (p.Leu451Met)
n.425C>A
12g.52676400G>ACA6586190KRT1c.1350C>T (p.Ala450=)
n.424C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52676400G>CCA479873572KRT1c.1350C>G (p.Ala450=)
n.424C>G
12g.52676400G=CA2036619614KRT1c.1350C= (p.Ala450=)
n.424C=
12g.52676400G>TCA479873574KRT1c.1350C>A (p.Ala450=)
n.424C>A
12g.52676401G>ACA384962841KRT1c.1349C>T (p.Ala450Val)
n.423C>T
12g.52676401G>CCA6586191KRT1c.1349C>G (p.Ala450Gly)
n.423C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52676401G=CA2036619615KRT1c.1349C= (p.Ala450=)
n.423C=
12g.52676401G>TCA384962844KRT1c.1349C>A (p.Ala450Asp)
n.423C>A
ClinVar dbSNP
12g.52676402C>ACA384962847KRT1c.1348G>T (p.Ala450Ser)
n.422G>T
12g.52676402C>GCA384962848KRT1c.1348G>C (p.Ala450Pro)
n.422G>C
12g.52676402C>TCA384962849KRT1c.1348G>A (p.Ala450Thr)
n.422G>A
gnomAD v4
12g.52676403A>CCA384962850KRT1c.1347T>G (p.Asp449Glu)
n.421T>G
12g.52676403A>GCA479873594KRT1c.1347T>C (p.Asp449=)
n.421T>C
12g.52676403A>TCA384962853KRT1c.1347T>A (p.Asp449Glu)
n.421T>A
12g.52676404T>ACA6586192KRT1c.1346A>T (p.Asp449Val)
n.420A>T
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52676404T>CCA384962862KRT1c.1346A>G (p.Asp449Gly)
n.420A>G
12g.52676404T>GCA384962865KRT1c.1346A>C (p.Asp449Ala)
n.420A>C
12g.52676404T=CA2036619616KRT1c.1346A= (p.Asp449=)
n.420A=
12g.52676405C>ACA384962880KRT1c.1345G>T (p.Asp449Tyr)
n.419G>T
12g.52676405C>GCA384962890KRT1c.1345G>C (p.Asp449His)
n.419G>C
12g.52676405C>TCA384962892KRT1c.1345G>A (p.Asp449Asn)
n.419G>A
12g.52676406C>ACA384962894KRT1c.1344G>T (p.Glu448Asp)
n.418G>T
12g.52676406C=CA2036619617KRT1c.1344G= (p.Glu448=)
n.418G=
12g.52676406C>GCA384962896KRT1c.1344G>C (p.Glu448Asp)
n.418G>C
12g.52676406C>TCA479873614KRT1c.1344G>A (p.Glu448=)
n.418G>A
dbSNP gnomAD v3 gnomAD v4
12g.52676407T>ACA384962902KRT1c.1343A>T (p.Glu448Val)
n.417A>T
12g.52676407T>CCA384962907KRT1c.1343A>G (p.Glu448Gly)
n.417A>G
12g.52676407T>GCA384962910KRT1c.1343A>C (p.Glu448Ala)
n.417A>C
12g.52676408C>ACA384962913KRT1c.1342G>T (p.Glu448Ter)
n.416G>T
12g.52676408C=CA2036619618KRT1c.1342G= (p.Glu448=)
n.416G=
12g.52676408C>GCA384962915KRT1c.1342G>C (p.Glu448Gln)
n.416G>C
dbSNP gnomAD v4
12g.52676408C>TCA384962917KRT1c.1342G>A (p.Glu448Lys)
n.416G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.52676409C>ACA479873631KRT1c.1341G>T (p.Leu447=)
n.415G>T
12g.52676409C>GCA479873628KRT1c.1341G>C (p.Leu447=)
n.415G>C
12g.52676409C>TCA479873626KRT1c.1341G>A (p.Leu447=)
n.415G>A
gnomAD v4
12g.52676410A=CA2036619619KRT1c.1340T= (p.Leu447=)
n.414T=
12g.52676410A>CCA384962921KRT1c.1340T>G (p.Leu447Arg)
n.414T>G
12g.52676410A>GCA384962926KRT1c.1340T>C (p.Leu447Pro)
n.414T>C
dbSNP
12g.52676410A>TCA384962928KRT1c.1340T>A (p.Leu447Gln)
n.414T>A
12g.52676411G>ACA479873636KRT1c.1339C>T (p.Leu447=)
n.413C>T
12g.52676411G>CCA384962929KRT1c.1339C>G (p.Leu447Val)
n.413C>G
12g.52676411G>TCA384962930KRT1c.1339C>A (p.Leu447Met)
n.413C>A
12g.52676412G>ACA479873639KRT1c.1338C>T (p.Asp446=)
n.412C>T
gnomAD v4
12g.52676412G>CCA384962931KRT1c.1338C>G (p.Asp446Glu)
n.412C>G
12g.52676412G>TCA384962934KRT1c.1338C>A (p.Asp446Glu)
n.412C>A
dbSNP
12g.52676413T>ACA384962937KRT1c.1337A>T (p.Asp446Val)
n.411A>T
dbSNP
12g.52676413T>CCA384962944KRT1c.1337A>G (p.Asp446Gly)
n.411A>G
12g.52676413T>GCA384962942KRT1c.1337A>C (p.Asp446Ala)
n.411A>C
dbSNP
12g.52676413T=CA2036619620KRT1c.1337A= (p.Asp446=)
n.411A=
12g.52676414C>ACA384962950KRT1c.1336G>T (p.Asp446Tyr)
n.410G>T
12g.52676414C>GCA384962957KRT1c.1336G>C (p.Asp446His)
n.410G>C
dbSNP
12g.52676414C>TCA384962960KRT1c.1336G>A (p.Asp446Asn)
n.410G>A
12g.52676415A>CCA384962961KRT1c.1335T>G (p.Asn445Lys)
n.409T>G
12g.52676415A>GCA479873660KRT1c.1335T>C (p.Asn445=)
n.409T>C
gnomAD v4
12g.52676415A>TCA384962963KRT1c.1335T>A (p.Asn445Lys)
n.409T>A
12g.52676416T>ACA384962970KRT1c.1334A>T (p.Asn445Ile)
n.408A>T
12g.52676416T>CCA384962975KRT1c.1334A>G (p.Asn445Ser)
n.408A>G
12g.52676416T>GCA384962979KRT1c.1334A>C (p.Asn445Thr)
n.408A>C
12g.52676417T>ACA384962982KRT1c.1333A>T (p.Asn445Tyr)
n.407A>T
12g.52676417T>CCA384962987KRT1c.1333A>G (p.Asn445Asp)
n.407A>G
12g.52676417T>GCA384962992KRT1c.1333A>C (p.Asn445His)
n.407A>C
12g.52676418C>ACA479873672KRT1c.1332G>T (p.Leu444=)
n.406G>T
12g.52676418C>GCA479873674KRT1c.1332G>C (p.Leu444=)
n.406G>C
12g.52676418C>TCA479873675KRT1c.1332G>A (p.Leu444=)
n.406G>A
dbSNP COSMIC
12g.52676419A>CCA384963014KRT1c.1331T>G (p.Leu444Arg)
n.405T>G
12g.52676419A>GCA384963009KRT1c.1331T>C (p.Leu444Pro)
n.405T>C
12g.52676419A>TCA384962998KRT1c.1331T>A (p.Leu444Gln)
n.405T>A
12g.52676420G>ACA479873682KRT1c.1330C>T (p.Leu444=)
n.404C>T
gnomAD v4
12g.52676420G>CCA384963020KRT1c.1330C>G (p.Leu444Val)
n.404C>G
12g.52676420G>TCA384963032KRT1c.1330C>A (p.Leu444Met)
n.404C>A
gnomAD v4
12g.52676421C>ACA384963040KRT1c.1329G>T (p.Lys443Asn)
n.403G>T
12g.52676421C>GCA384963052KRT1c.1329G>C (p.Lys443Asn)
n.403G>C
12g.52676421C>TCA479873689KRT1c.1329G>A (p.Lys443=)
n.403G>A
gnomAD v4
12g.52676422T>ACA6586193KRT1c.1328A>T (p.Lys443Met)
n.402A>T
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52676422T>CCA384963057KRT1c.1328A>G (p.Lys443Arg)
n.402A>G
12g.52676422T>GCA384963058KRT1c.1328A>C (p.Lys443Thr)
n.402A>C
12g.52676422T=CA2036619621KRT1c.1328A= (p.Lys443=)
n.402A=
12g.52676423T>ACA384963061KRT1c.1327A>T (p.Lys443Ter)
n.401A>T
12g.52676423T>CCA384963074KRT1c.1327A>G (p.Lys443Glu)
n.401A>G
12g.52676423T>GCA384963076KRT1c.1327A>C (p.Lys443Gln)
n.401A>C
12g.52676424G>ACA479873697KRT1c.1326C>T (p.Asn442=)
n.400C>T
gnomAD v4
12g.52676424G>CCA384963078KRT1c.1326C>G (p.Asn442Lys)
n.400C>G
dbSNP gnomAD v2
12g.52676424G=CA2036619622KRT1c.1326C= (p.Asn442=)
n.400C=
12g.52676424G>TCA384963079KRT1c.1326C>A (p.Asn442Lys)
n.400C>A
12g.52676425T>ACA384963093KRT1c.1325A>T (p.Asn442Ile)
n.399A>T
12g.52676425T>CCA384963087KRT1c.1325A>G (p.Asn442Ser)
n.399A>G
12g.52676425T>GCA384963081KRT1c.1325A>C (p.Asn442Thr)
n.399A>C
12g.52676426T>ACA384963106KRT1c.1324A>T (p.Asn442Tyr)
n.398A>T
gnomAD v4
12g.52676426T>CCA384963119KRT1c.1324A>G (p.Asn442Asp)
n.398A>G
12g.52676426T>GCA384963113KRT1c.1324A>C (p.Asn442His)
n.398A>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.52676426T=CA2036619623KRT1c.1324A= (p.Asn442=)
n.398A=
12g.52676427C>ACA384963127KRT1c.1323G>T (p.Lys441Asn)
n.397G>T
COSMIC
12g.52676427C=CA2036619624KRT1c.1323G= (p.Lys441=)
n.397G=
12g.52676427C>GCA384963142KRT1c.1323G>C (p.Lys441Asn)
n.397G>C
12g.52676427C>TCA237262540KRT1c.1323G>A (p.Lys441=)
n.397G>A
dbSNP gnomAD v4
12g.52676428T>ACA384963155KRT1c.1322A>T (p.Lys441Met)
n.396A>T
12g.52676428T>CCA384963164KRT1c.1322A>G (p.Lys441Arg)
n.396A>G
12g.52676428T>GCA384963167KRT1c.1322A>C (p.Lys441Thr)
n.396A>C
12g.52676429T>ACA384963170KRT1c.1321A>T (p.Lys441Ter)
n.395A>T
12g.52676429T>CCA384963176KRT1c.1321A>G (p.Lys441Glu)
n.395A>G
12g.52676429T>GCA384963178KRT1c.1321A>C (p.Lys441Gln)
n.395A>C
12g.52676430G>ACA479873731KRT1c.1320C>T (p.Ala440=)
n.394C>T
12g.52676430G>CCA479873732KRT1c.1320C>G (p.Ala440=)
n.394C>G
12g.52676430G>TCA479873734KRT1c.1320C>A (p.Ala440=)
n.394C>A
12g.52676435_52676446dupCA2573148760KRT1c.1309_1320dup (p.Ala440_Lys441insLeuLysAspAla)
n.383_394dup
ClinVar dbSNP
12g.52676431G>ACA384963212KRT1c.1319C>T (p.Ala440Val)
n.393C>T
12g.52676431G>CCA384963189KRT1c.1319C>G (p.Ala440Gly)
n.393C>G
12g.52676431G>TCA384963207KRT1c.1319C>A (p.Ala440Asp)
n.393C>A
12g.52676431_52676432delinsATCA2695216818KRT1c.1318_1319delinsAT (p.Ala440Ile)
n.392_393delinsAT
12g.52676432C>ACA6586194KRT1c.1318G>T (p.Ala440Ser)
n.392G>T
dbSNP ExAC gnomAD v2 gnomAD v4
12g.52676432C=CA2036619625KRT1c.1318G= (p.Ala440=)
n.392G=
12g.52676432C>GCA384963222KRT1c.1318G>C (p.Ala440Pro)
n.392G>C
12g.52676432C>TCA384963228KRT1c.1318G>A (p.Ala440Thr)
n.392G>A
ClinVar
12g.52676433A>CCA384963233KRT1c.1317T>G (p.Asp439Glu)
n.391T>G
12g.52676433A>GCA479873747KRT1c.1317T>C (p.Asp439=)
n.391T>C
12g.52676433A>TCA384963250KRT1c.1317T>A (p.Asp439Glu)
n.391T>A
12g.52676434T>ACA384963265KRT1c.1316A>T (p.Asp439Val)
n.390A>T
12g.52676434T>CCA6586195KRT1c.1316A>G (p.Asp439Gly)
n.390A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.52676434T>GCA384963254KRT1c.1316A>C (p.Asp439Ala)
n.390A>C
12g.52676434T=CA2036619626KRT1c.1316A= (p.Asp439=)
n.390A=

Number of alleles fetched