Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.133352479C>ACA375693664SURF1c.718G>T (p.Gly240Cys)
n.628G>T
n.708G>T
c.391G>T (p.Gly131Cys)
9g.133352479C>GCA375693665SURF1c.718G>C (p.Gly240Arg)
n.628G>C
n.708G>C
c.391G>C (p.Gly131Arg)
9g.133352479C>TCA375693666SURF1c.718G>A (p.Gly240Ser)
n.628G>A
n.708G>A
c.391G>A (p.Gly131Ser)
9g.133352480T>CCA860707812SURF1c.717A>G (p.Thr239=)
n.627A>G
n.707A>G
c.390A>G (p.Thr130=)
dbSNP
9g.133352480T=CA1882634088SURF1c.717A= (p.Thr239=)
n.627A=
n.707A=
c.390A= (p.Thr130=)
9g.133352481G>ACA375693669SURF1c.716C>T (p.Thr239Ile)
n.626C>T
n.706C>T
c.389C>T (p.Thr130Ile)
dbSNP gnomAD v3 gnomAD v4
9g.133352481G>CCA375693668SURF1c.716C>G (p.Thr239Arg)
n.626C>G
n.706C>G
c.389C>G (p.Thr130Arg)
9g.133352481G=CA1882634091SURF1c.716C= (p.Thr239=)
n.626C=
n.706C=
c.389C= (p.Thr130=)
9g.133352481G>TCA375693667SURF1c.716C>A (p.Thr239Lys)
n.626C>A
n.706C>A
c.389C>A (p.Thr130Lys)
9g.133352482T>ACA375693670SURF1c.715A>T (p.Thr239Ser)
n.625A>T
n.705A>T
c.388A>T (p.Thr130Ser)
9g.133352482T>CCA375693671SURF1c.715A>G (p.Thr239Ala)
n.625A>G
n.705A>G
c.388A>G (p.Thr130Ala)
9g.133352482T>GCA375693672SURF1c.715A>C (p.Thr239Pro)
n.625A>C
n.705A>C
c.388A>C (p.Thr130Pro)
9g.133352483G>CCA375693673SURF1c.714C>G (p.Ile238Met)
n.624C>G
n.704C>G
c.387C>G (p.Ile129Met)
9g.133352484A=CA1882634096SURF1c.713T= (p.Ile238=)
n.623T=
n.703T=
c.386T= (p.Ile129=)
9g.133352484A>CCA375693674SURF1c.713T>G (p.Ile238Ser)
n.623T>G
n.703T>G
c.386T>G (p.Ile129Ser)
dbSNP gnomAD v4
9g.133352484A>GCA375693675SURF1c.713T>C (p.Ile238Thr)
n.623T>C
n.703T>C
c.386T>C (p.Ile129Thr)
ClinVar dbSNP
9g.133352484A>TCA375693676SURF1c.713T>A (p.Ile238Asn)
n.623T>A
n.703T>A
c.386T>A (p.Ile129Asn)
9g.133352485T>ACA375693677SURF1c.712A>T (p.Ile238Phe)
n.622A>T
n.702A>T
c.385A>T (p.Ile129Phe)
9g.133352485T>CCA375693678SURF1c.712A>G (p.Ile238Val)
n.622A>G
n.702A>G
c.385A>G (p.Ile129Val)
gnomAD v4
9g.133352485T>GCA375693679SURF1c.712A>C (p.Ile238Leu)
n.622A>C
n.702A>C
c.385A>C (p.Ile129Leu)
9g.133352486T>ACA375693680SURF1c.711A>T (p.Arg237Ser)
n.621A>T
n.701A>T
c.384A>T (p.Arg128Ser)
9g.133352486T>GCA375693681SURF1c.711A>C (p.Arg237Ser)
n.621A>C
n.701A>C
c.384A>C (p.Arg128Ser)
9g.133352487C>ACA375693684SURF1c.710G>T (p.Arg237Ile)
n.620G>T
n.700G>T
c.383G>T (p.Arg128Ile)
9g.133352487C>GCA375693683SURF1c.710G>C (p.Arg237Thr)
n.620G>C
n.700G>C
c.383G>C (p.Arg128Thr)
9g.133352487C>TCA375693682SURF1c.710G>A (p.Arg237Lys)
n.620G>A
n.700G>A
c.383G>A (p.Arg128Lys)
9g.133352488T>ACA375693685SURF1c.709A>T (p.Arg237Ter)
n.619A>T
n.699A>T
c.382A>T (p.Arg128Ter)
9g.133352488T>CCA200832350SURF1c.709A>G (p.Arg237Gly)
n.619A>G
n.699A>G
c.382A>G (p.Arg128Gly)
dbSNP
9g.133352488T>GCA1882634099SURF1c.709A>C (p.Arg237=)
n.619A>C
n.699A>C
c.382A>C (p.Arg128=)
dbSNP
9g.133352488T=CA1882634101SURF1c.709A= (p.Arg237=)
n.619A=
n.699A=
c.382A= (p.Arg128=)
9g.133352489G>ACA200832352SURF1c.708C>T (p.Ala236=)
n.618C>T
n.698C>T
c.381C>T (p.Ala127=)
ClinVar dbSNP gnomAD v4
9g.133352489G=CA1882634103SURF1c.708C= (p.Ala236=)
n.618C=
n.698C=
c.381C= (p.Ala127=)
9g.133352489G>TCA200832353SURF1c.708C>A (p.Ala236=)
n.618C>A
n.698C>A
c.381C>A (p.Ala127=)
ClinVar dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352490G>ACA375693686SURF1c.707C>T (p.Ala236Val)
n.617C>T
n.697C>T
c.380C>T (p.Ala127Val)
ClinVar dbSNP
9g.133352490G>CCA375693687SURF1c.707C>G (p.Ala236Gly)
n.617C>G
n.697C>G
c.380C>G (p.Ala127Gly)
dbSNP
9g.133352490G=CA1882634106SURF1c.707C= (p.Ala236=)
n.617C=
n.697C=
c.380C= (p.Ala127=)
9g.133352490G>TCA375693688SURF1c.707C>A (p.Ala236Asp)
n.617C>A
n.697C>A
c.380C>A (p.Ala127Asp)
9g.133352491C>ACA375693690SURF1c.706G>T (p.Ala236Ser)
n.616G>T
n.696G>T
c.379G>T (p.Ala127Ser)
9g.133352491C=CA1882634115SURF1c.706G= (p.Ala236=)
n.616G=
n.696G=
c.379G= (p.Ala127=)
9g.133352491C>GCA375693689SURF1c.706G>C (p.Ala236Pro)
n.616G>C
n.696G>C
c.379G>C (p.Ala127Pro)
9g.133352491C>TCA200832355SURF1c.706G>A (p.Ala236Thr)
n.616G>A
n.696G>A
c.379G>A (p.Ala127Thr)
ClinVar dbSNP dbSNP gnomAD v4
9g.133352492C>ACA375693691SURF1c.705G>T (p.Met235Ile)
n.615G>T
n.695G>T
c.378G>T (p.Met126Ile)
gnomAD v4
9g.133352492C>GCA375693692SURF1c.705G>C (p.Met235Ile)
n.615G>C
n.695G>C
c.378G>C (p.Met126Ile)
9g.133352492C>TCA375693693SURF1c.705G>A (p.Met235Ile)
n.615G>A
n.695G>A
c.378G>A (p.Met126Ile)
9g.133352493A=CA1882634120SURF1c.704T= (p.Met235=)
n.614T=
n.694T=
c.377T= (p.Met126=)
9g.133352493A>CCA375693694SURF1c.704T>G (p.Met235Arg)
n.614T>G
n.694T>G
c.377T>G (p.Met126Arg)
9g.133352493A>GCA375693695SURF1c.704T>C (p.Met235Thr)
n.614T>C
n.694T>C
c.377T>C (p.Met126Thr)
dbSNP gnomAD v4
9g.133352493A>TCA375693696SURF1c.704T>A (p.Met235Lys)
n.614T>A
n.694T>A
c.377T>A (p.Met126Lys)
9g.133352494T>ACA375693697SURF1c.703A>T (p.Met235Leu)
n.613A>T
n.693A>T
c.376A>T (p.Met126Leu)
9g.133352494T>CCA375693698SURF1c.703A>G (p.Met235Val)
n.613A>G
n.693A>G
c.376A>G (p.Met126Val)
ClinVar dbSNP dbSNP gnomAD v4
9g.133352494T>GCA200832358SURF1c.703A>C (p.Met235Leu)
n.613A>C
n.693A>C
c.376A>C (p.Met126Leu)
ClinVar dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352494T=CA1882634122SURF1c.703A= (p.Met235=)
n.613A=
n.693A=
c.376A= (p.Met126=)
9g.133352495A=CA1882634126SURF1c.702T= (p.Ala234=)
n.612T=
n.692T=
c.375T= (p.Ala125=)
9g.133352495A>GCA860707839SURF1c.702T>C (p.Ala234=)
n.612T>C
n.692T>C
c.375T>C (p.Ala125=)
dbSNP gnomAD v4
9g.133352496G>ACA375693699SURF1c.701C>T (p.Ala234Val)
n.611C>T
n.691C>T
c.374C>T (p.Ala125Val)
9g.133352496G>CCA375693700SURF1c.701C>G (p.Ala234Gly)
n.611C>G
n.691C>G
c.374C>G (p.Ala125Gly)
9g.133352496G>TCA375693701SURF1c.701C>A (p.Ala234Asp)
n.611C>A
n.691C>A
c.374C>A (p.Ala125Asp)
9g.133352497C>ACA375693702SURF1c.700G>T (p.Ala234Ser)
n.610G>T
n.690G>T
c.373G>T (p.Ala125Ser)
9g.133352497C=CA1882634128SURF1c.700G= (p.Ala234=)
n.610G=
n.690G=
c.373G= (p.Ala125=)
9g.133352497C>GCA375693703SURF1c.700G>C (p.Ala234Pro)
n.610G>C
n.690G>C
c.373G>C (p.Ala125Pro)
ClinVar dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352497C>TCA200832360SURF1c.700G>A (p.Ala234Thr)
n.610G>A
n.690G>A
c.373G>A (p.Ala125Thr)
ClinVar dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352498T>ACA375693704SURF1c.699A>T (p.Glu233Asp)
n.609A>T
n.689A>T
c.372A>T (p.Glu124Asp)
9g.133352498T>CCA1129731698SURF1c.699A>G (p.Glu233=)
n.609A>G
n.689A>G
c.372A>G (p.Glu124=)
gnomAD v3 gnomAD v4
9g.133352498T>GCA375693705SURF1c.699A>C (p.Glu233Asp)
n.609A>C
n.689A>C
c.372A>C (p.Glu124Asp)
9g.133352499T>ACA375693706SURF1c.698A>T (p.Glu233Val)
n.608A>T
n.688A>T
c.371A>T (p.Glu124Val)
9g.133352499T>CCA375693707SURF1c.698A>G (p.Glu233Gly)
n.608A>G
n.688A>G
c.371A>G (p.Glu124Gly)
9g.133352499T>GCA375693708SURF1c.698A>C (p.Glu233Ala)
n.608A>C
n.688A>C
c.371A>C (p.Glu124Ala)
9g.133352500C>ACA375693710SURF1c.697G>T (p.Glu233Ter)
n.607G>T
n.687G>T
c.370G>T (p.Glu124Ter)
9g.133352500C=CA1882634130SURF1c.697G= (p.Glu233=)
n.607G=
n.687G=
c.370G= (p.Glu124=)
9g.133352500C>GCA200832364SURF1c.697G>C (p.Glu233Gln)
n.607G>C
n.687G>C
c.370G>C (p.Glu124Gln)
dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352500C>TCA375693709SURF1c.697G>A (p.Glu233Lys)
n.607G>A
n.687G>A
c.370G>A (p.Glu124Lys)
9g.133352501C>TCA2692339039SURF1c.696G>A (p.Leu232=)
n.606G>A
n.686G>A
c.369G>A (p.Leu123=)
gnomAD v4
9g.133352502A>CCA375693711SURF1c.695T>G (p.Leu232Arg)
n.605T>G
n.685T>G
c.368T>G (p.Leu123Arg)
9g.133352502A>GCA375693713SURF1c.695T>C (p.Leu232Pro)
n.605T>C
n.685T>C
c.368T>C (p.Leu123Pro)
gnomAD v4
9g.133352502A>TCA375693712SURF1c.695T>A (p.Leu232Gln)
n.605T>A
n.685T>A
c.368T>A (p.Leu123Gln)
9g.133352503G>ACA200832365SURF1c.694C>T (p.Leu232=)
n.604C>T
n.684C>T
c.367C>T (p.Leu123=)
ClinVar dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352503G>CCA375693714SURF1c.694C>G (p.Leu232Val)
n.604C>G
n.684C>G
c.367C>G (p.Leu123Val)
9g.133352503G=CA1882634132SURF1c.694C= (p.Leu232=)
n.604C=
n.684C=
c.367C= (p.Leu123=)
9g.133352503G>TCA375693715SURF1c.694C>A (p.Leu232Met)
n.604C>A
n.684C>A
c.367C>A (p.Leu123Met)
9g.133352506_133352523delCA2695211588SURF1c.677_694del (p.His226_Asp231del)
n.587_604del
n.667_684del
c.350_367del (p.His117_Asp122del)
9g.133352504G>ACA860707863SURF1c.693C>T (p.Asp231=)
n.603C>T
n.683C>T
c.366C>T (p.Asp122=)
dbSNP dbSNP gnomAD v4
9g.133352504G>CCA200832368SURF1c.693C>G (p.Asp231Glu)
n.603C>G
n.683C>G
c.366C>G (p.Asp122Glu)
ClinVar dbSNP gnomAD v4
9g.133352504G=CA1882634136SURF1c.693C= (p.Asp231=)
n.603C=
n.683C=
c.366C= (p.Asp122=)
9g.133352504G>TCA375693716SURF1c.693C>A (p.Asp231Glu)
n.603C>A
n.683C>A
c.366C>A (p.Asp122Glu)
9g.133352505T>ACA375693717SURF1c.692A>T (p.Asp231Val)
n.602A>T
n.682A>T
c.365A>T (p.Asp122Val)
9g.133352505T>CCA375693718SURF1c.692A>G (p.Asp231Gly)
n.602A>G
n.682A>G
c.365A>G (p.Asp122Gly)
ClinVar gnomAD v4
9g.133352505T>GCA375693719SURF1c.692A>C (p.Asp231Ala)
n.602A>C
n.682A>C
c.365A>C (p.Asp122Ala)
9g.133352506C>ACA375693720SURF1c.691G>T (p.Asp231Tyr)
n.601G>T
n.681G>T
c.364G>T (p.Asp122Tyr)
9g.133352506C>GCA375693721SURF1c.691G>C (p.Asp231His)
n.601G>C
n.681G>C
c.364G>C (p.Asp122His)
9g.133352506C>TCA375693722SURF1c.691G>A (p.Asp231Asn)
n.601G>A
n.681G>A
c.364G>A (p.Asp122Asn)
9g.133352508C>ACA375693725SURF1c.689G>T (p.Arg230Leu)
n.599G>T
n.679G>T
c.362G>T (p.Arg121Leu)
9g.133352508C=CA1882634140SURF1c.689G= (p.Arg230=)
n.599G=
n.679G=
c.362G= (p.Arg121=)
9g.133352508C>GCA375693723SURF1c.689G>C (p.Arg230Pro)
n.599G>C
n.679G>C
c.362G>C (p.Arg121Pro)
dbSNP
9g.133352508C>TCA375693724SURF1c.689G>A (p.Arg230Gln)
n.599G>A
n.679G>A
c.362G>A (p.Arg121Gln)
dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352509G>ACA10603164SURF1c.688C>T (p.Arg230Ter)
n.598C>T
n.678C>T
c.361C>T (p.Arg121Ter)
ClinVar dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352509G>CCA375693726SURF1c.688C>G (p.Arg230Gly)
n.598C>G
n.678C>G
c.361C>G (p.Arg121Gly)
9g.133352509G=CA1882634144SURF1c.688C= (p.Arg230=)
n.598C=
n.678C=
c.361C= (p.Arg121=)
9g.133352509G>TCA2786166145SURF1c.688C>A (p.Arg230=)
n.598C>A
n.678C>A
c.361C>A (p.Arg121=)
9g.133352509_133352511delCA2692339062SURF1c.686_688del (p.Tyr229Ter)
n.596_598del
n.676_678del
c.359_361del (p.Tyr120Ter)
gnomAD v4
9g.133352509_133352515delCA2695211589SURF1c.682_688del (p.His228GlufsTer?)
n.592_598del
n.672_678del
c.355_361del (p.His119GlufsTer?)
9g.133352510A=CA1882634149SURF1c.687T= (p.Tyr229=)
n.597T=
n.677T=
c.360T= (p.Tyr120=)
9g.133352510A>CCA375693727SURF1c.687T>G (p.Tyr229Ter)
n.597T>G
n.677T>G
c.360T>G (p.Tyr120Ter)
9g.133352510A>GCA200832370SURF1c.687T>C (p.Tyr229=)
n.597T>C
n.677T>C
c.360T>C (p.Tyr120=)
ClinVar dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352510A>TCA375693728SURF1c.687T>A (p.Tyr229Ter)
n.597T>A
n.677T>A
c.360T>A (p.Tyr120Ter)
9g.133352512_133352514delCA2692339066SURF1c.685_687del (p.Tyr229del)
n.595_597del
n.675_677del
c.358_360del (p.Tyr120del)
gnomAD v4
9g.133352511T>ACA375693729SURF1c.686A>T (p.Tyr229Phe)
n.596A>T
n.676A>T
c.359A>T (p.Tyr120Phe)
9g.133352511T>CCA375693730SURF1c.686A>G (p.Tyr229Cys)
n.596A>G
n.676A>G
c.359A>G (p.Tyr120Cys)
9g.133352511T>GCA375693731SURF1c.686A>C (p.Tyr229Ser)
n.596A>C
n.676A>C
c.359A>C (p.Tyr120Ser)
9g.133352512A>CCA375693732SURF1c.685T>G (p.Tyr229Asp)
n.595T>G
n.675T>G
c.358T>G (p.Tyr120Asp)
9g.133352512A>GCA375693733SURF1c.685T>C (p.Tyr229His)
n.595T>C
n.675T>C
c.358T>C (p.Tyr120His)
9g.133352512A>TCA375693734SURF1c.685T>A (p.Tyr229Asn)
n.595T>A
n.675T>A
c.358T>A (p.Tyr120Asn)
9g.133352513A>CCA375693736SURF1c.684T>G (p.His228Gln)
n.594T>G
n.674T>G
c.357T>G (p.His119Gln)
COSMIC
9g.133352513A>TCA375693735SURF1c.684T>A (p.His228Gln)
n.594T>A
n.674T>A
c.357T>A (p.His119Gln)
ClinVar
9g.133352514T>ACA375693737SURF1c.683A>T (p.His228Leu)
n.593A>T
n.673A>T
c.356A>T (p.His119Leu)
9g.133352514T>CCA200832371SURF1c.683A>G (p.His228Arg)
n.593A>G
n.673A>G
c.356A>G (p.His119Arg)
dbSNP gnomAD v4
9g.133352514T>GCA375693738SURF1c.683A>C (p.His228Pro)
n.593A>C
n.673A>C
c.356A>C (p.His119Pro)
9g.133352514T=CA1882634153SURF1c.683A= (p.His228=)
n.593A=
n.673A=
c.356A= (p.His119=)
9g.133352515G>ACA375693739SURF1c.682C>T (p.His228Tyr)
n.592C>T
n.672C>T
c.355C>T (p.His119Tyr)
9g.133352515G>CCA375693740SURF1c.682C>G (p.His228Asp)
n.592C>G
n.672C>G
c.355C>G (p.His119Asp)
9g.133352515G>TCA375693741SURF1c.682C>A (p.His228Asn)
n.592C>A
n.672C>A
c.355C>A (p.His119Asn)
9g.133352516C>ACA375693742SURF1c.681G>T (p.Trp227Cys)
n.591G>T
n.671G>T
c.354G>T (p.Trp118Cys)
9g.133352516C=CA1882634157SURF1c.681G= (p.Trp227=)
n.591G=
n.671G=
c.354G= (p.Trp118=)
9g.133352516C>GCA375693743SURF1c.681G>C (p.Trp227Cys)
n.591G>C
n.671G>C
c.354G>C (p.Trp118Cys)
9g.133352516C>TCA16605403SURF1c.681G>A (p.Trp227Ter)
n.591G>A
n.671G>A
c.354G>A (p.Trp118Ter)
ClinVar dbSNP gnomAD v4
9g.133352517C>ACA375693744SURF1c.680G>T (p.Trp227Leu)
n.590G>T
n.670G>T
c.353G>T (p.Trp118Leu)
9g.133352517C>GCA375693745SURF1c.680G>C (p.Trp227Ser)
n.590G>C
n.670G>C
c.353G>C (p.Trp118Ser)
9g.133352517C>TCA375693746SURF1c.680G>A (p.Trp227Ter)
n.590G>A
n.670G>A
c.353G>A (p.Trp118Ter)
gnomAD v4
9g.133352518A=CA1882634161SURF1c.679T= (p.Trp227=)
n.589T=
n.669T=
c.352T= (p.Trp118=)
9g.133352518A>CCA375693748SURF1c.679T>G (p.Trp227Gly)
n.589T>G
n.669T>G
c.352T>G (p.Trp118Gly)
9g.133352518A>GCA128719SURF1c.679T>C (p.Trp227Arg)
n.589T>C
n.669T>C
c.352T>C (p.Trp118Arg)
ClinVar dbSNP
9g.133352518A>TCA375693747SURF1c.679T>A (p.Trp227Arg)
n.589T>A
n.669T>A
c.352T>A (p.Trp118Arg)
ClinVar dbSNP
9g.133352519G>ACA2573144047SURF1c.678C>T (p.His226=)
n.588C>T
n.668C>T
c.351C>T (p.His117=)
ClinVar dbSNP gnomAD v4
9g.133352519G>CCA375693749SURF1c.678C>G (p.His226Gln)
n.588C>G
n.668C>G
c.351C>G (p.His117Gln)
9g.133352519G>TCA375693750SURF1c.678C>A (p.His226Gln)
n.588C>A
n.668C>A
c.351C>A (p.His117Gln)
gnomAD v4
9g.133352520T>ACA375693751SURF1c.677A>T (p.His226Leu)
n.587A>T
n.667A>T
c.350A>T (p.His117Leu)
9g.133352520T>CCA375693752SURF1c.677A>G (p.His226Arg)
n.587A>G
n.667A>G
c.350A>G (p.His117Arg)
9g.133352520T>GCA375693753SURF1c.677A>C (p.His226Pro)
n.587A>C
n.667A>C
c.350A>C (p.His117Pro)
9g.133352521G>ACA375693754SURF1c.676C>T (p.His226Tyr)
n.586C>T
n.666C>T
c.349C>T (p.His117Tyr)
gnomAD v4
9g.133352521G>CCA375693755SURF1c.676C>G (p.His226Asp)
n.586C>G
n.666C>G
c.349C>G (p.His117Asp)
9g.133352521G>TCA375693756SURF1c.676C>A (p.His226Asn)
n.586C>A
n.666C>A
c.349C>A (p.His117Asn)
9g.133352522G>ACA2692339089SURF1c.675C>T (p.Asn225=)
n.585C>T
n.665C>T
c.348C>T (p.Asn116=)
gnomAD v4
9g.133352522G>CCA375693757SURF1c.675C>G (p.Asn225Lys)
n.585C>G
n.665C>G
c.348C>G (p.Asn116Lys)
9g.133352522G>TCA375693758SURF1c.675C>A (p.Asn225Lys)
n.585C>A
n.665C>A
c.348C>A (p.Asn116Lys)
9g.133352523T>ACA375693759SURF1c.674A>T (p.Asn225Ile)
n.584A>T
n.664A>T
c.347A>T (p.Asn116Ile)
9g.133352523T>CCA375693760SURF1c.674A>G (p.Asn225Ser)
n.584A>G
n.664A>G
c.347A>G (p.Asn116Ser)
9g.133352523T>GCA375693761SURF1c.674A>C (p.Asn225Thr)
n.584A>C
n.664A>C
c.347A>C (p.Asn116Thr)
9g.133352524T>ACA375693763SURF1c.673A>T (p.Asn225Tyr)
n.583A>T
n.663A>T
c.346A>T (p.Asn116Tyr)
9g.133352524T>CCA375693764SURF1c.673A>G (p.Asn225Asp)
n.583A>G
n.663A>G
c.346A>G (p.Asn116Asp)
9g.133352524T>GCA375693762SURF1c.673A>C (p.Asn225His)
n.583A>C
n.663A>C
c.346A>C (p.Asn116His)
9g.133352525C>ACA375693766SURF1c.672G>T (p.Arg224Ser)
n.582G>T
n.662G>T
c.345G>T (p.Arg115Ser)
9g.133352525C>GCA375693765SURF1c.672G>C (p.Arg224Ser)
n.582G>C
n.662G>C
c.345G>C (p.Arg115Ser)
9g.133352525C>TCA2579498334SURF1c.672G>A (p.Arg224=)
n.582G>A
n.662G>A
c.345G>A (p.Arg115=)
9g.133352526C>ACA375693767SURF1c.671G>T (p.Arg224Met)
n.581G>T
n.661G>T
c.344G>T (p.Arg115Met)
9g.133352526C>GCA375693768SURF1c.671G>C (p.Arg224Thr)
n.581G>C
n.661G>C
c.344G>C (p.Arg115Thr)
9g.133352526C>TCA375693769SURF1c.671G>A (p.Arg224Lys)
n.581G>A
n.661G>A
c.344G>A (p.Arg115Lys)
9g.133352527T>ACA375693770SURF1c.670A>T (p.Arg224Trp)
n.580A>T
n.660A>T
c.343A>T (p.Arg115Trp)
9g.133352527T>CCA200832375SURF1c.670A>G (p.Arg224Gly)
n.580A>G
n.660A>G
c.343A>G (p.Arg115Gly)
dbSNP dbSNP gnomAD v4
9g.133352527T=CA1882634166SURF1c.670A= (p.Arg224=)
n.580A=
n.660A=
c.343A= (p.Arg115=)
9g.133352528T>ACA375693772SURF1c.669A>T (p.Glu223Asp)
n.579A>T
n.659A>T
c.342A>T (p.Glu114Asp)
9g.133352528T>GCA375693771SURF1c.669A>C (p.Glu223Asp)
n.579A>C
n.659A>C
c.342A>C (p.Glu114Asp)
gnomAD v4
9g.133352529T>ACA375693773SURF1c.668A>T (p.Glu223Val)
n.578A>T
n.658A>T
c.341A>T (p.Glu114Val)
9g.133352529T>CCA200832378SURF1c.668A>G (p.Glu223Gly)
n.578A>G
n.658A>G
c.341A>G (p.Glu114Gly)
ClinVar dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352529T>GCA375693774SURF1c.668A>C (p.Glu223Ala)
n.578A>C
n.658A>C
c.341A>C (p.Glu114Ala)
9g.133352529T=CA1882634168SURF1c.668A= (p.Glu223=)
n.578A=
n.658A=
c.341A= (p.Glu114=)
9g.133352530C>ACA375693775SURF1c.667G>T (p.Glu223Ter)
n.577G>T
n.657G>T
c.340G>T (p.Glu114Ter)
9g.133352530C>GCA375693776SURF1c.667G>C (p.Glu223Gln)
n.577G>C
n.657G>C
c.340G>C (p.Glu114Gln)
9g.133352530C>TCA375693777SURF1c.667G>A (p.Glu223Lys)
n.577G>A
n.657G>A
c.340G>A (p.Glu114Lys)
9g.133352532G>ACA375693780SURF1c.665C>T (p.Pro222Leu)
n.575C>T
n.655C>T
c.338C>T (p.Pro113Leu)
ClinVar gnomAD v4
9g.133352532G>CCA375693778SURF1c.665C>G (p.Pro222Arg)
n.575C>G
n.655C>G
c.338C>G (p.Pro113Arg)
ClinVar gnomAD v4
9g.133352532G>TCA375693779SURF1c.665C>A (p.Pro222Gln)
n.575C>A
n.655C>A
c.338C>A (p.Pro113Gln)
9g.133352533G>ACA375693781SURF1c.664C>T (p.Pro222Ser)
n.574C>T
n.654C>T
c.337C>T (p.Pro113Ser)
dbSNP dbSNP gnomAD v4
9g.133352533G>CCA375693782SURF1c.664C>G (p.Pro222Ala)
n.574C>G
n.654C>G
c.337C>G (p.Pro113Ala)
gnomAD v4
9g.133352533G=CA1882634171SURF1c.664C= (p.Pro222=)
n.574C=
n.654C=
c.337C= (p.Pro113=)
9g.133352533G>TCA375693783SURF1c.664C>A (p.Pro222Thr)
n.574C>A
n.654C>A
c.337C>A (p.Pro113Thr)
gnomAD v4
9g.133352534A=CA1882634172SURF1c.663T= (p.Asn221=)
n.573T=
n.653T=
c.336T= (p.Asn112=)
9g.133352534A>CCA375693784SURF1c.663T>G (p.Asn221Lys)
n.573T>G
n.653T>G
c.336T>G (p.Asn112Lys)
dbSNP gnomAD v4
9g.133352534A>TCA375693785SURF1c.663T>A (p.Asn221Lys)
n.573T>A
n.653T>A
c.336T>A (p.Asn112Lys)
9g.133352535T>ACA375693786SURF1c.662A>T (p.Asn221Ile)
n.572A>T
n.652A>T
c.335A>T (p.Asn112Ile)
9g.133352535T>CCA375693787SURF1c.662A>G (p.Asn221Ser)
n.572A>G
n.652A>G
c.335A>G (p.Asn112Ser)
gnomAD v4
9g.133352535T>GCA375693788SURF1c.662A>C (p.Asn221Thr)
n.572A>C
n.652A>C
c.335A>C (p.Asn112Thr)
9g.133352536T>ACA375693789SURF1c.661A>T (p.Asn221Tyr)
n.571A>T
n.651A>T
c.334A>T (p.Asn112Tyr)
9g.133352536T>CCA375693790SURF1c.661A>G (p.Asn221Asp)
n.571A>G
n.651A>G
c.334A>G (p.Asn112Asp)
ClinVar gnomAD v4
9g.133352536T>GCA375693791SURF1c.661A>C (p.Asn221His)
n.571A>C
n.651A>C
c.334A>C (p.Asn112His)
9g.133352537G>ACA2550311936SURF1c.660C>T (p.Asn220=)
n.570C>T
n.650C>T
c.333C>T (p.Asn111=)
gnomAD v4
9g.133352537G>CCA375693792SURF1c.660C>G (p.Asn220Lys)
n.570C>G
n.650C>G
c.333C>G (p.Asn111Lys)
9g.133352537G>TCA375693793SURF1c.660C>A (p.Asn220Lys)
n.570C>A
n.650C>A
c.333C>A (p.Asn111Lys)
9g.133352538T>ACA375693794SURF1c.659A>T (p.Asn220Ile)
n.569A>T
n.649A>T
c.332A>T (p.Asn111Ile)
9g.133352538T>CCA375693796SURF1c.659A>G (p.Asn220Ser)
n.569A>G
n.649A>G
c.332A>G (p.Asn111Ser)
9g.133352538T>GCA375693795SURF1c.659A>C (p.Asn220Thr)
n.569A>C
n.649A>C
c.332A>C (p.Asn111Thr)
9g.133352539T>ACA375693797SURF1c.658A>T (p.Asn220Tyr)
n.568A>T
n.648A>T
c.331A>T (p.Asn111Tyr)
9g.133352539T>CCA375693798SURF1c.658A>G (p.Asn220Asp)
n.568A>G
n.648A>G
c.331A>G (p.Asn111Asp)
9g.133352539T>GCA375693799SURF1c.658A>C (p.Asn220His)
n.568A>C
n.648A>C
c.331A>C (p.Asn111His)
9g.133352541_133352542delCA2695211590SURF1c.657_658del (p.Asn220GlnfsTer27)
n.567_568del
n.647_648del
c.330_331del (p.Asn111GlnfsTer27)
ClinVar
9g.133352540delCA2786166146SURF1c.657del (p.Asn220ThrfsTer?)
n.567del
n.647del
c.330del (p.Asn111ThrfsTer?)
9g.133352540C>ACA375693800SURF1c.657G>T (p.Glu219Asp)
n.567G>T
n.647G>T
c.330G>T (p.Glu110Asp)
9g.133352540C=CA1882634175SURF1c.657G= (p.Glu219=)
n.567G=
n.647G=
c.330G= (p.Glu110=)
9g.133352540C>GCA375693801SURF1c.657G>C (p.Glu219Asp)
n.567G>C
n.647G>C
c.330G>C (p.Glu110Asp)
ClinVar gnomAD v4
9g.133352540C>TCA16605407SURF1c.657G>A (p.Glu219=)
n.567G>A
n.647G>A
c.330G>A (p.Glu110=)
ClinVar dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352541T>ACA375693802SURF1c.656A>T (p.Glu219Val)
n.566A>T
n.646A>T
c.329A>T (p.Glu110Val)
dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352541T>CCA375693803SURF1c.656A>G (p.Glu219Gly)
n.566A>G
n.646A>G
c.329A>G (p.Glu110Gly)
9g.133352541T>GCA375693804SURF1c.656A>C (p.Glu219Ala)
n.566A>C
n.646A>C
c.329A>C (p.Glu110Ala)
9g.133352541T=CA1882634179SURF1c.656A= (p.Glu219=)
n.566A=
n.646A=
c.329A= (p.Glu110=)
9g.133352542C>ACA375693805SURF1c.655G>T (p.Glu219Ter)
n.565G>T
n.645G>T
c.328G>T (p.Glu110Ter)
9g.133352542C=CA1882634184SURF1c.655G= (p.Glu219=)
n.565G=
n.645G=
c.328G= (p.Glu110=)
9g.133352542C>GCA375693806SURF1c.655G>C (p.Glu219Gln)
n.565G>C
n.645G>C
c.328G>C (p.Glu110Gln)
ClinVar
9g.133352542C>TCA375693807SURF1c.655G>A (p.Glu219Lys)
n.565G>A
n.645G>A
c.328G>A (p.Glu110Lys)
dbSNP gnomAD v4
9g.133352542_133352544delinsCAGCA1882634182SURF1c.653_655delinsCTG (p.Pro218=)
n.563_565delinsCTG
n.643_645delinsCTG
c.326_328delinsCTG (p.Pro109=)
9g.133352543A=CA1882634186SURF1c.654T= (p.Pro218=)
n.564T=
n.644T=
c.327T= (p.Pro109=)
9g.133352543A>CCA2507646506SURF1c.654T>G (p.Pro218=)
n.564T>G
n.644T>G
c.327T>G (p.Pro109=)
9g.133352543A>GCA1882634188SURF1c.654T>C (p.Pro218=)
n.564T>C
n.644T>C
c.327T>C (p.Pro109=)
ClinVar dbSNP gnomAD v4
9g.133352543_133352544delCA860707959SURF1c.653_654del (p.Pro218ArgfsTer29)
n.563_564del
n.643_644del
c.326_327del (p.Pro109ArgfsTer29)
dbSNP gnomAD v4
9g.133352544G>ACA375693810SURF1c.653C>T (p.Pro218Leu)
n.563C>T
n.643C>T
c.326C>T (p.Pro109Leu)
dbSNP gnomAD v4
9g.133352544G>CCA375693809SURF1c.653C>G (p.Pro218Arg)
n.563C>G
n.643C>G
c.326C>G (p.Pro109Arg)
9g.133352544G=CA1882634190SURF1c.653C= (p.Pro218=)
n.563C=
n.643C=
c.326C= (p.Pro109=)
9g.133352544G>TCA375693808SURF1c.653C>A (p.Pro218His)
n.563C>A
n.643C>A
c.326C>A (p.Pro109His)
9g.133352545G>ACA375693811SURF1c.652C>T (p.Pro218Ser)
n.562C>T
n.642C>T
c.325C>T (p.Pro109Ser)
9g.133352545G>CCA375693812SURF1c.652C>G (p.Pro218Ala)
n.562C>G
n.642C>G
c.325C>G (p.Pro109Ala)
9g.133352545G>TCA375693813SURF1c.652C>A (p.Pro218Thr)
n.562C>A
n.642C>A
c.325C>A (p.Pro109Thr)
9g.133352546G>ACA200832380SURF1c.651C>T (p.Val217=)
n.561C>T
n.641C>T
c.324C>T (p.Val108=)
dbSNP gnomAD v4
9g.133352546G=CA1882634193SURF1c.651C= (p.Val217=)
n.561C=
n.641C=
c.324C= (p.Val108=)
9g.133352547A=CA1882634196SURF1c.650T= (p.Val217=)
n.560T=
n.640T=
c.323T= (p.Val108=)
9g.133352547A>CCA375693814SURF1c.650T>G (p.Val217Gly)
n.560T>G
n.640T>G
c.323T>G (p.Val108Gly)
9g.133352547A>GCA200832382SURF1c.650T>C (p.Val217Ala)
n.560T>C
n.640T>C
c.323T>C (p.Val108Ala)
dbSNP
9g.133352547A>TCA375693815SURF1c.650T>A (p.Val217Asp)
n.560T>A
n.640T>A
c.323T>A (p.Val108Asp)
9g.133352548C>ACA375693816SURF1c.649G>T (p.Val217Phe)
n.559G>T
n.639G>T
c.322G>T (p.Val108Phe)
9g.133352548C=CA1882634199SURF1c.649G= (p.Val217=)
n.559G=
n.639G=
c.322G= (p.Val108=)
9g.133352548C>GCA375693817SURF1c.649G>C (p.Val217Leu)
n.559G>C
n.639G>C
c.322G>C (p.Val108Leu)
9g.133352548C>TCA375693818SURF1c.649G>A (p.Val217Ile)
n.559G>A
n.639G>A
c.322G>A (p.Val108Ile)
ClinVar dbSNP
9g.133352549A>CCA375693819SURF1c.648T>G (p.Phe216Leu)
n.558T>G
n.638T>G
c.321T>G (p.Phe107Leu)
9g.133352549A>GCA2739265142SURF1c.648T>C (p.Phe216=)
n.558T>C
n.638T>C
c.321T>C (p.Phe107=)
ClinVar
9g.133352549A>TCA375693820SURF1c.648T>A (p.Phe216Leu)
n.558T>A
n.638T>A
c.321T>A (p.Phe107Leu)
9g.133352550A>CCA375693823SURF1c.647T>G (p.Phe216Cys)
n.557T>G
n.637T>G
c.320T>G (p.Phe107Cys)
9g.133352550A>GCA375693822SURF1c.647T>C (p.Phe216Ser)
n.557T>C
n.637T>C
c.320T>C (p.Phe107Ser)
gnomAD v4 COSMIC
9g.133352550A>TCA375693821SURF1c.647T>A (p.Phe216Tyr)
n.557T>A
n.637T>A
c.320T>A (p.Phe107Tyr)
9g.133352551A>CCA375693824SURF1c.646T>G (p.Phe216Val)
n.556T>G
n.636T>G
c.319T>G (p.Phe107Val)
9g.133352551A>GCA375693826SURF1c.646T>C (p.Phe216Leu)
n.556T>C
n.636T>C
c.319T>C (p.Phe107Leu)
9g.133352551A>TCA375693825SURF1c.646T>A (p.Phe216Ile)
n.556T>A
n.636T>A
c.319T>A (p.Phe107Ile)
9g.133352552A>GCA2533655184SURF1c.645T>C (p.Pro215=)
n.555T>C
n.635T>C
c.318T>C (p.Pro106=)
9g.133352552A>TCA2692339155SURF1c.645T>A (p.Pro215=)
n.555T>A
n.635T>A
c.318T>A (p.Pro106=)
gnomAD v4
9g.133352553G>ACA200832385SURF1c.644C>T (p.Pro215Leu)
n.554C>T
n.634C>T
c.317C>T (p.Pro106Leu)
dbSNP gnomAD v4
9g.133352553G>CCA375693827SURF1c.644C>G (p.Pro215Arg)
n.554C>G
n.634C>G
c.317C>G (p.Pro106Arg)
9g.133352553G=CA1882634201SURF1c.644C= (p.Pro215=)
n.554C=
n.634C=
c.317C= (p.Pro106=)
9g.133352553G>TCA375693828SURF1c.644C>A (p.Pro215His)
n.554C>A
n.634C>A
c.317C>A (p.Pro106His)
9g.133352554G>ACA375693829SURF1c.643C>T (p.Pro215Ser)
n.553C>T
n.633C>T
c.316C>T (p.Pro106Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4
9g.133352554G>CCA10629367SURF1c.643C>G (p.Pro215Ala)
n.553C>G
n.633C>G
c.316C>G (p.Pro106Ala)
ClinVar dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352554G=CA1882634209SURF1c.643C= (p.Pro215=)
n.553C=
n.633C=
c.316C= (p.Pro106=)
9g.133352554G>TCA375693830SURF1c.643C>A (p.Pro215Thr)
n.553C>A
n.633C>A
c.316C>A (p.Pro106Thr)
dbSNP gnomAD v4
9g.133352556_133352558delCA2573144048SURF1c.641_643del (p.Gln214del)
n.551_553del
n.631_633del
c.314_316del (p.Gln105del)
ClinVar dbSNP
9g.133352554_133352565delinsGCTGCCTGGTTTCA1882634205SURF1c.632_643delinsAAACCAGGCAGC (p.Glu211=)
n.542_553delinsAAACCAGGCAGC
n.622_633delinsAAACCAGGCAGC
c.305_316delinsAAACCAGGCAGC (p.Glu102=)
9g.133352555C>ACA375693831SURF1c.642G>T (p.Gln214His)
n.552G>T
n.632G>T
c.315G>T (p.Gln105His)
COSMIC
9g.133352555C>GCA375693832SURF1c.642G>C (p.Gln214His)
n.552G>C
n.632G>C
c.315G>C (p.Gln105His)
9g.133352558_133352568delCA200832387SURF1c.632_642del (p.Glu211AlafsTer5)
n.542_552del
n.622_632del
c.305_315del (p.Glu102AlafsTer5)
ClinVar dbSNP dbSNP
9g.133352556T>ACA375693833SURF1c.641A>T (p.Gln214Leu)
n.551A>T
n.631A>T
c.314A>T (p.Gln105Leu)
9g.133352556T>CCA200832390SURF1c.641A>G (p.Gln214Arg)
n.551A>G
n.631A>G
c.314A>G (p.Gln105Arg)
dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352556T>GCA375693834SURF1c.641A>C (p.Gln214Pro)
n.551A>C
n.631A>C
c.314A>C (p.Gln105Pro)
9g.133352556T=CA1882634213SURF1c.641A= (p.Gln214=)
n.551A=
n.631A=
c.314A= (p.Gln105=)
9g.133352557G>ACA375693835SURF1c.640C>T (p.Gln214Ter)
n.550C>T
n.630C>T
c.313C>T (p.Gln105Ter)
ClinVar dbSNP gnomAD v4
9g.133352557G>CCA375693837SURF1c.640C>G (p.Gln214Glu)
n.550C>G
n.630C>G
c.313C>G (p.Gln105Glu)
9g.133352557G>TCA375693836SURF1c.640C>A (p.Gln214Lys)
n.550C>A
n.630C>A
c.313C>A (p.Gln105Lys)
COSMIC
9g.133352558C>ACA375693838SURF1c.639G>T (p.Arg213Ser)
n.549G>T
n.629G>T
c.312G>T (p.Arg104Ser)
9g.133352558C>GCA375693839SURF1c.639G>C (p.Arg213Ser)
n.549G>C
n.629G>C
c.312G>C (p.Arg104Ser)
9g.133352558C>TCA2692339177SURF1c.639G>A (p.Arg213=)
n.549G>A
n.629G>A
c.312G>A (p.Arg104=)
ClinVar gnomAD v4
9g.133352559C>ACA375693840SURF1c.638G>T (p.Arg213Met)
n.548G>T
n.628G>T
c.311G>T (p.Arg104Met)
9g.133352559C=CA1882634215SURF1c.638G= (p.Arg213=)
n.548G=
n.628G=
c.311G= (p.Arg104=)
9g.133352559C>GCA375693841SURF1c.638G>C (p.Arg213Thr)
n.548G>C
n.628G>C
c.311G>C (p.Arg104Thr)
ClinVar dbSNP gnomAD v3 gnomAD v4
9g.133352559C>TCA375693842SURF1c.638G>A (p.Arg213Lys)
n.548G>A
n.628G>A
c.311G>A (p.Arg104Lys)
gnomAD v4
9g.133352560T>ACA375693843SURF1c.637A>T (p.Arg213Trp)
n.547A>T
n.627A>T
c.310A>T (p.Arg104Trp)
9g.133352560T>CCA375693844SURF1c.637A>G (p.Arg213Gly)
n.547A>G
n.627A>G
c.310A>G (p.Arg104Gly)
gnomAD v4
9g.133352560T>GCA2523467952SURF1c.637A>C (p.Arg213=)
n.547A>C
n.627A>C
c.310A>C (p.Arg104=)
9g.133352561G>ACA860708021SURF1c.636C>T (p.Thr212=)
n.546C>T
n.626C>T
c.309C>T (p.Thr103=)
ClinVar dbSNP dbSNP gnomAD v4
9g.133352561G>CCA1882634219SURF1c.636C>G (p.Thr212=)
n.546C>G
n.626C>G
c.309C>G (p.Thr103=)
dbSNP
9g.133352561G=CA1882634218SURF1c.636C= (p.Thr212=)
n.546C=
n.626C=
c.309C= (p.Thr103=)
9g.133352562delCA2695211591SURF1c.636del (p.Arg213GlyfsTer?)
n.546del
n.626del
c.309del (p.Arg104GlyfsTer?)
9g.133352562G>ACA375693845SURF1c.635C>T (p.Thr212Ile)
n.545C>T
n.625C>T
c.308C>T (p.Thr103Ile)
9g.133352562G>CCA375693846SURF1c.635C>G (p.Thr212Ser)
n.545C>G
n.625C>G
c.308C>G (p.Thr103Ser)
gnomAD v4
9g.133352562G>TCA375693847SURF1c.635C>A (p.Thr212Asn)
n.545C>A
n.625C>A
c.308C>A (p.Thr103Asn)
9g.133352563T>ACA375693849SURF1c.634A>T (p.Thr212Ser)
n.544A>T
n.624A>T
c.307A>T (p.Thr103Ser)
9g.133352563T>CCA375693850SURF1c.634A>G (p.Thr212Ala)
n.544A>G
n.624A>G
c.307A>G (p.Thr103Ala)
gnomAD v4
9g.133352563T>GCA375693848SURF1c.634A>C (p.Thr212Pro)
n.544A>C
n.624A>C
c.307A>C (p.Thr103Pro)
9g.133352564T>ACA375693851SURF1c.633A>T (p.Glu211Asp)
n.543A>T
n.623A>T
c.306A>T (p.Glu102Asp)
9g.133352564T>CCA2500303988SURF1c.633A>G (p.Glu211=)
n.543A>G
n.623A>G
c.306A>G (p.Glu102=)
9g.133352564T>GCA375693852SURF1c.633A>C (p.Glu211Asp)
n.543A>C
n.623A>C
c.306A>C (p.Glu102Asp)
gnomAD v4
9g.133352564_133352566delinsTTCCA1882634221SURF1c.631_633delinsGAA (p.Glu211=)
n.541_543delinsGAA
n.621_623delinsGAA
c.304_306delinsGAA (p.Glu102=)
9g.133352565T>ACA375693853SURF1c.632A>T (p.Glu211Val)
n.542A>T
n.622A>T
c.305A>T (p.Glu102Val)
gnomAD v4
9g.133352565T>CCA375693854SURF1c.632A>G (p.Glu211Gly)
n.542A>G
n.622A>G
c.305A>G (p.Glu102Gly)
dbSNP dbSNP gnomAD v4
9g.133352565T>GCA375693855SURF1c.632A>C (p.Glu211Ala)
n.542A>C
n.622A>C
c.305A>C (p.Glu102Ala)
9g.133352565T=CA1882634225SURF1c.632A= (p.Glu211=)
n.542A=
n.622A=
c.305A= (p.Glu102=)
9g.133352566_133352567delCA658683555SURF1c.631_632del (p.Glu211AsnfsTer8)
n.541_542del
n.621_622del
c.304_305del (p.Glu102AsnfsTer8)
ClinVar dbSNP
9g.133352566C>ACA375693858SURF1c.631G>T (p.Glu211Ter)
n.541G>T
n.621G>T
c.304G>T (p.Glu102Ter)
gnomAD v4
9g.133352566C>GCA375693857SURF1c.631G>C (p.Glu211Gln)
n.541G>C
n.621G>C
c.304G>C (p.Glu102Gln)
9g.133352566C>TCA375693856SURF1c.631G>A (p.Glu211Lys)
n.541G>A
n.621G>A
c.304G>A (p.Glu102Lys)
9g.133352567T>CCA860708042SURF1c.630A>G (p.Thr210=)
n.540A>G
n.620A>G
c.303A>G (p.Thr101=)
ClinVar dbSNP dbSNP gnomAD v3 gnomAD v4
9g.133352567T=CA1882634228SURF1c.630A= (p.Thr210=)
n.540A=
n.620A=
c.303A= (p.Thr101=)
9g.133352568G>ACA375693859SURF1c.629C>T (p.Thr210Ile)
n.539C>T
n.619C>T
c.302C>T (p.Thr101Ile)
ClinVar dbSNP gnomAD v3 gnomAD v4
9g.133352568G>CCA375693860SURF1c.629C>G (p.Thr210Arg)
n.539C>G
n.619C>G
c.302C>G (p.Thr101Arg)
9g.133352568G=CA1882634230SURF1c.629C= (p.Thr210=)
n.539C=
n.619C=
c.302C= (p.Thr101=)
9g.133352568G>TCA375693861SURF1c.629C>A (p.Thr210Lys)
n.539C>A
n.619C>A
c.302C>A (p.Thr101Lys)
9g.133352569T>ACA375693862SURF1c.628A>T (p.Thr210Ser)
n.538A>T
n.618A>T
c.301A>T (p.Thr101Ser)
9g.133352569T>CCA375693863SURF1c.628A>G (p.Thr210Ala)
n.538A>G
n.618A>G
c.301A>G (p.Thr101Ala)
9g.133352569T>GCA375693864SURF1c.628A>C (p.Thr210Pro)
n.538A>C
n.618A>C
c.301A>C (p.Thr101Pro)
9g.133352570C>TCA2697558159SURF1c.627G>A (p.Leu209=)
n.537G>A
n.617G>A
c.300G>A (p.Leu100=)
ClinVar
9g.133352571A>CCA375693865SURF1c.626T>G (p.Leu209Arg)
n.536T>G
n.616T>G
c.299T>G (p.Leu100Arg)
9g.133352571A>GCA375693867SURF1c.626T>C (p.Leu209Pro)
n.536T>C
n.616T>C
c.299T>C (p.Leu100Pro)
9g.133352571A>TCA375693866SURF1c.626T>A (p.Leu209Gln)
n.536T>A
n.616T>A
c.299T>A (p.Leu100Gln)
9g.133352572G>CCA375693868SURF1c.625C>G (p.Leu209Val)
n.535C>G
n.615C>G
c.298C>G (p.Leu100Val)
dbSNP gnomAD v4
9g.133352572G=CA1882634232SURF1c.625C= (p.Leu209=)
n.535C=
n.615C=
c.298C= (p.Leu100=)
9g.133352572G>TCA375693869SURF1c.625C>A (p.Leu209Met)
n.535C>A
n.615C>A
c.298C>A (p.Leu100Met)
9g.133352573C>ACA375693870SURF1c.624G>T (p.Arg208Ser)
n.534G>T
n.614G>T
c.297G>T (p.Arg99Ser)
9g.133352573C>GCA375693871SURF1c.624G>C (p.Arg208Ser)
n.534G>C
n.614G>C
c.297G>C (p.Arg99Ser)
9g.133352574C>ACA375693872SURF1c.623G>T (p.Arg208Met)
n.533G>T
n.613G>T
c.296G>T (p.Arg99Met)
9g.133352574C=CA1882634234SURF1c.623G= (p.Arg208=)
n.533G=
n.613G=
c.296G= (p.Arg99=)
9g.133352574C>GCA375693873SURF1c.623G>C (p.Arg208Thr)
n.533G>C
n.613G>C
c.296G>C (p.Arg99Thr)
9g.133352574C>TCA375693874SURF1c.623G>A (p.Arg208Lys)
n.533G>A
n.613G>A
c.296G>A (p.Arg99Lys)
dbSNP gnomAD v4
9g.133352575delCA2695211592SURF1c.622del (p.Arg208GlyfsTer2)
n.532del
n.612del
c.295del (p.Arg99GlyfsTer2)
9g.133352575T>ACA375693875SURF1c.622A>T (p.Arg208Trp)
n.532A>T
n.612A>T
c.295A>T (p.Arg99Trp)
9g.133352575T>CCA375693876SURF1c.622A>G (p.Arg208Gly)
n.532A>G
n.612A>G
c.295A>G (p.Arg99Gly)
9g.133352576C=CA1882634236SURF1c.621G= (p.Val207=)
n.531G=
n.611G=
c.294G= (p.Val98=)
9g.133352576C>TCA200832393SURF1c.621G>A (p.Val207=)
n.531G>A
n.611G>A
c.294G>A (p.Val98=)
ClinVar dbSNP gnomAD v4
9g.133352577A>CCA375693877SURF1c.620T>G (p.Val207Gly)
n.530T>G
n.610T>G
c.293T>G (p.Val98Gly)
9g.133352577A>GCA375693878SURF1c.620T>C (p.Val207Ala)
n.530T>C
n.610T>C
c.293T>C (p.Val98Ala)
9g.133352577A>TCA375693879SURF1c.620T>A (p.Val207Glu)
n.530T>A
n.610T>A
c.293T>A (p.Val98Glu)
9g.133352578C>ACA375693881SURF1c.619G>T (p.Val207Leu)
n.529G>T
n.609G>T
c.292G>T (p.Val98Leu)
9g.133352578C=CA1882634239SURF1c.619G= (p.Val207=)
n.529G=
n.609G=
c.292G= (p.Val98=)
9g.133352578C>GCA375693882SURF1c.619G>C (p.Val207Leu)
n.529G>C
n.609G>C
c.292G>C (p.Val98Leu)
9g.133352578C>TCA375693880SURF1c.619G>A (p.Val207Met)
n.529G>A
n.609G>A
c.292G>A (p.Val98Met)
dbSNP gnomAD v3 gnomAD v4
9g.133352579C>ACA375693883SURF1c.618G>T (p.Met206Ile)
n.528G>T
n.608G>T
c.291G>T (p.Met97Ile)
9g.133352579C>GCA375693885SURF1c.618G>C (p.Met206Ile)
n.528G>C
n.608G>C
c.291G>C (p.Met97Ile)
9g.133352579C>TCA375693884SURF1c.618G>A (p.Met206Ile)
n.528G>A
n.608G>A
c.291G>A (p.Met97Ile)

Number of alleles fetched