Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.65057624delCA2679288048EYSc.2127del (p.Pro710HisfsTer19)
gnomAD v4
6g.65057624A=CA1634036131EYSc.2127T= (p.Pro709=)
6g.65057624A>CCA450765808EYSc.2127T>G (p.Pro709=)
6g.65057624A>GCA450765809EYSc.2127T>C (p.Pro709=)
gnomAD v4
6g.65057624A>TCA450765810EYSc.2127T>A (p.Pro709=)
dbSNP gnomAD v2 gnomAD v4
6g.65057625G>ACA364787381EYSc.2126C>T (p.Pro709Leu)
6g.65057625G>CCA364787384EYSc.2126C>G (p.Pro709Arg)
6g.65057625G>TCA364787386EYSc.2126C>A (p.Pro709His)
gnomAD v4
6g.65057626delCA450765811EYSc.2126del (p.Pro709LeufsTer20)
COSMIC
6g.65057626G>ACA364787388EYSc.2125C>T (p.Pro709Ser)
dbSNP gnomAD v3 gnomAD v4
6g.65057626G>CCA364787391EYSc.2125C>G (p.Pro709Ala)
6g.65057626G=CA1634036134EYSc.2125C= (p.Pro709=)
6g.65057626G>TCA364787393EYSc.2125C>A (p.Pro709Thr)
dbSNP gnomAD v2 gnomAD v4
6g.65057627C>ACA450765812EYSc.2124G>T (p.Val708=)
6g.65057627C>GCA450765814EYSc.2124G>C (p.Val708=)
6g.65057627C>TCA450765813EYSc.2124G>A (p.Val708=)
ClinVar dbSNP
6g.65057628A=CA1634036140EYSc.2123T= (p.Val708=)
6g.65057628A>CCA364787410EYSc.2123T>G (p.Val708Gly)
6g.65057628A>GCA364787413EYSc.2123T>C (p.Val708Ala)
dbSNP gnomAD v3 gnomAD v4
6g.65057628A>TCA364787415EYSc.2123T>A (p.Val708Glu)
6g.65057629C>ACA364787418EYSc.2122G>T (p.Val708Leu)
6g.65057629C>GCA364787420EYSc.2122G>C (p.Val708Leu)
6g.65057629C>TCA364787422EYSc.2122G>A (p.Val708Met)
6g.65057630A>CCA364787427EYSc.2121T>G (p.Cys707Trp)
6g.65057630A>GCA450765815EYSc.2121T>C (p.Cys707=)
6g.65057630A>TCA364787424EYSc.2121T>A (p.Cys707Ter)
6g.65057631C>ACA364787431EYSc.2120G>T (p.Cys707Phe)
6g.65057631C>GCA364787433EYSc.2120G>C (p.Cys707Ser)
6g.65057631C>TCA364787435EYSc.2120G>A (p.Cys707Tyr)
6g.65057632A>CCA364787439EYSc.2119T>G (p.Cys707Gly)
6g.65057632A>GCA364787441EYSc.2119T>C (p.Cys707Arg)
gnomAD v4
6g.65057632A>TCA364787442EYSc.2119T>A (p.Cys707Ser)
6g.65057633C>ACA364787446EYSc.2118G>T (p.Gln706His)
6g.65057633C>GCA364787448EYSc.2118G>C (p.Gln706His)
6g.65057633C>TCA450765816EYSc.2118G>A (p.Gln706=)
6g.65057634T>ACA364787450EYSc.2117A>T (p.Gln706Leu)
6g.65057634T>CCA364787452EYSc.2117A>G (p.Gln706Arg)
6g.65057634T>GCA364787454EYSc.2117A>C (p.Gln706Pro)
6g.65057635G>ACA364787458EYSc.2116C>T (p.Gln706Ter)
gnomAD v4
6g.65057635G>CCA364787460EYSc.2116C>G (p.Gln706Glu)
6g.65057635G>TCA364787462EYSc.2116C>A (p.Gln706Lys)
6g.65057636G>ACA450765817EYSc.2115C>T (p.Cys705=)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.65057636G>CCA364787467EYSc.2115C>G (p.Cys705Trp)
6g.65057636G=CA1634036144EYSc.2115C= (p.Cys705=)
6g.65057636G>TCA364787464EYSc.2115C>A (p.Cys705Ter)
6g.65057637C>ACA140397900EYSc.2114G>T (p.Cys705Phe)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.65057637C=CA1634036146EYSc.2114G= (p.Cys705=)
6g.65057637C>GCA364787471EYSc.2114G>C (p.Cys705Ser)
6g.65057637C>TCA364787473EYSc.2114G>A (p.Cys705Tyr)
6g.65057638A=CA1634036149EYSc.2113T= (p.Cys705=)

Number of alleles fetched