Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.26475359C>ACA346109737OTOFc.3126G>T (p.Met1042Ile)
c.885G>T (p.Met295Ile)
c.1056G>T (p.Met352Ile)
c.3171G>T (p.Met1057Ile)
2g.26475359C>GCA346109739OTOFc.3126G>C (p.Met1042Ile)
c.885G>C (p.Met295Ile)
c.1056G>C (p.Met352Ile)
c.3171G>C (p.Met1057Ile)
2g.26475359C>TCA346109740OTOFc.3126G>A (p.Met1042Ile)
c.885G>A (p.Met295Ile)
c.1056G>A (p.Met352Ile)
c.3171G>A (p.Met1057Ile)
2g.26475360A>CCA346109749OTOFc.3125T>G (p.Met1042Arg)
c.884T>G (p.Met295Arg)
c.1055T>G (p.Met352Arg)
c.3170T>G (p.Met1057Arg)
2g.26475360A>GCA346109742OTOFc.3125T>C (p.Met1042Thr)
c.884T>C (p.Met295Thr)
c.1055T>C (p.Met352Thr)
c.3170T>C (p.Met1057Thr)
gnomAD v4
2g.26475360A>TCA346109744OTOFc.3125T>A (p.Met1042Lys)
c.884T>A (p.Met295Lys)
c.1055T>A (p.Met352Lys)
c.3170T>A (p.Met1057Lys)
2g.26475361T>ACA346109752OTOFc.3124A>T (p.Met1042Leu)
c.883A>T (p.Met295Leu)
c.1054A>T (p.Met352Leu)
c.3169A>T (p.Met1057Leu)
2g.26475361T>CCA185178OTOFc.3124A>G (p.Met1042Val)
c.883A>G (p.Met295Val)
c.1054A>G (p.Met352Val)
c.3169A>G (p.Met1057Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.26475361T>GCA346109754OTOFc.3124A>C (p.Met1042Leu)
c.883A>C (p.Met295Leu)
c.1054A>C (p.Met352Leu)
c.3169A>C (p.Met1057Leu)
2g.26475361T=CA1239827058OTOFc.3124A= (p.Met1042=)
c.883A= (p.Met295=)
c.1054A= (p.Met352=)
c.3169A= (p.Met1057=)
2g.26475362G>ACA425204003OTOFc.3123C>T (p.Ser1041=)
c.882C>T (p.Ser294=)
c.1053C>T (p.Ser351=)
c.3168C>T (p.Ser1056=)
gnomAD v4
2g.26475362G>CCA425204004OTOFc.3123C>G (p.Ser1041=)
c.882C>G (p.Ser294=)
c.1053C>G (p.Ser351=)
c.3168C>G (p.Ser1056=)
2g.26475362G>TCA425204005OTOFc.3123C>A (p.Ser1041=)
c.882C>A (p.Ser294=)
c.1053C>A (p.Ser351=)
c.3168C>A (p.Ser1056=)
2g.26475363G>ACA44397601OTOFc.3122C>T (p.Ser1041Phe)
c.881C>T (p.Ser294Phe)
c.1052C>T (p.Ser351Phe)
c.3167C>T (p.Ser1056Phe)
dbSNP
2g.26475363G>CCA346109759OTOFc.3122C>G (p.Ser1041Cys)
c.881C>G (p.Ser294Cys)
c.1052C>G (p.Ser351Cys)
c.3167C>G (p.Ser1056Cys)
2g.26475363G=CA1239827065OTOFc.3122C= (p.Ser1041=)
c.881C= (p.Ser294=)
c.1052C= (p.Ser351=)
c.3167C= (p.Ser1056=)
2g.26475363G>TCA346109761OTOFc.3122C>A (p.Ser1041Tyr)
c.881C>A (p.Ser294Tyr)
c.1052C>A (p.Ser351Tyr)
c.3167C>A (p.Ser1056Tyr)
2g.26475364A>CCA346109764OTOFc.3121T>G (p.Ser1041Ala)
c.880T>G (p.Ser294Ala)
c.1051T>G (p.Ser351Ala)
c.3166T>G (p.Ser1056Ala)
2g.26475364A>GCA346109768OTOFc.3121T>C (p.Ser1041Pro)
c.880T>C (p.Ser294Pro)
c.1051T>C (p.Ser351Pro)
c.3166T>C (p.Ser1056Pro)
2g.26475364A>TCA346109771OTOFc.3121T>A (p.Ser1041Thr)
c.880T>A (p.Ser294Thr)
c.1051T>A (p.Ser351Thr)
c.3166T>A (p.Ser1056Thr)
2g.26475365A>CCA346109772OTOFc.3120T>G (p.Asp1040Glu)
c.879T>G (p.Asp293Glu)
c.1050T>G (p.Asp350Glu)
c.3165T>G (p.Asp1055Glu)
2g.26475365A>GCA425204006OTOFc.3120T>C (p.Asp1040=)
c.879T>C (p.Asp293=)
c.1050T>C (p.Asp350=)
c.3165T>C (p.Asp1055=)
2g.26475365A>TCA346109773OTOFc.3120T>A (p.Asp1040Glu)
c.879T>A (p.Asp293Glu)
c.1050T>A (p.Asp350Glu)
c.3165T>A (p.Asp1055Glu)
2g.26475366T>ACA346109780OTOFc.3119A>T (p.Asp1040Val)
c.878A>T (p.Asp293Val)
c.1049A>T (p.Asp350Val)
c.3164A>T (p.Asp1055Val)
2g.26475366T>CCA346109783OTOFc.3119A>G (p.Asp1040Gly)
c.878A>G (p.Asp293Gly)
c.1049A>G (p.Asp350Gly)
c.3164A>G (p.Asp1055Gly)
dbSNP
2g.26475366T>GCA346109778OTOFc.3119A>C (p.Asp1040Ala)
c.878A>C (p.Asp293Ala)
c.1049A>C (p.Asp350Ala)
c.3164A>C (p.Asp1055Ala)
2g.26475366T=CA1239827069OTOFc.3119A= (p.Asp1040=)
c.878A= (p.Asp293=)
c.1049A= (p.Asp350=)
c.3164A= (p.Asp1055=)
2g.26475367C>ACA346109784OTOFc.3118G>T (p.Asp1040Tyr)
c.877G>T (p.Asp293Tyr)
c.1048G>T (p.Asp350Tyr)
c.3163G>T (p.Asp1055Tyr)
2g.26475367C>GCA346109785OTOFc.3118G>C (p.Asp1040His)
c.877G>C (p.Asp293His)
c.1048G>C (p.Asp350His)
c.3163G>C (p.Asp1055His)
2g.26475367C>TCA346109786OTOFc.3118G>A (p.Asp1040Asn)
c.877G>A (p.Asp293Asn)
c.1048G>A (p.Asp350Asn)
c.3163G>A (p.Asp1055Asn)
gnomAD v4
2g.26475368C>ACA346109791OTOFc.3117G>T (p.Gln1039His)
c.876G>T (p.Gln292His)
c.1047G>T (p.Gln349His)
c.3162G>T (p.Gln1054His)
2g.26475368C>GCA346109792OTOFc.3117G>C (p.Gln1039His)
c.876G>C (p.Gln292His)
c.1047G>C (p.Gln349His)
c.3162G>C (p.Gln1054His)
2g.26475368C>TCA425204007OTOFc.3117G>A (p.Gln1039=)
c.876G>A (p.Gln292=)
c.1047G>A (p.Gln349=)
c.3162G>A (p.Gln1054=)
2g.26475369T>ACA346109801OTOFc.3116A>T (p.Gln1039Leu)
c.875A>T (p.Gln292Leu)
c.1046A>T (p.Gln349Leu)
c.3161A>T (p.Gln1054Leu)
2g.26475369T>CCA346109796OTOFc.3116A>G (p.Gln1039Arg)
c.875A>G (p.Gln292Arg)
c.1046A>G (p.Gln349Arg)
c.3161A>G (p.Gln1054Arg)
gnomAD v4
2g.26475369T>GCA346109798OTOFc.3116A>C (p.Gln1039Pro)
c.875A>C (p.Gln292Pro)
c.1046A>C (p.Gln349Pro)
c.3161A>C (p.Gln1054Pro)
2g.26475370G>ACA346109804OTOFc.3115C>T (p.Gln1039Ter)
c.874C>T (p.Gln292Ter)
c.1045C>T (p.Gln349Ter)
c.3160C>T (p.Gln1054Ter)
2g.26475370G>CCA346109807OTOFc.3115C>G (p.Gln1039Glu)
c.874C>G (p.Gln292Glu)
c.1045C>G (p.Gln349Glu)
c.3160C>G (p.Gln1054Glu)
2g.26475370G>TCA346109809OTOFc.3115C>A (p.Gln1039Lys)
c.874C>A (p.Gln292Lys)
c.1045C>A (p.Gln349Lys)
c.3160C>A (p.Gln1054Lys)
2g.26475371delCA2539487511OTOFc.3115del (p.Gln1039ArgfsTer19)
c.874del (p.Gln292ArgfsTer19)
c.1045del (p.Gln349ArgfsTer19)
c.3160del (p.Gln1054ArgfsTer19)
2g.26475371G>ACA425204008OTOFc.3114C>T (p.Asp1038=)
c.873C>T (p.Asp291=)
c.1044C>T (p.Asp348=)
c.3159C>T (p.Asp1053=)
2g.26475371G>CCA346109811OTOFc.3114C>G (p.Asp1038Glu)
c.873C>G (p.Asp291Glu)
c.1044C>G (p.Asp348Glu)
c.3159C>G (p.Asp1053Glu)
2g.26475371G=CA1239827073OTOFc.3114C= (p.Asp1038=)
c.873C= (p.Asp291=)
c.1044C= (p.Asp348=)
c.3159C= (p.Asp1053=)
2g.26475371G>TCA346109814OTOFc.3114C>A (p.Asp1038Glu)
c.873C>A (p.Asp291Glu)
c.1044C>A (p.Asp348Glu)
c.3159C>A (p.Asp1053Glu)
dbSNP
2g.26475372T>ACA346109817OTOFc.3113A>T (p.Asp1038Val)
c.872A>T (p.Asp291Val)
c.1043A>T (p.Asp348Val)
c.3158A>T (p.Asp1053Val)
2g.26475372T>CCA1563660OTOFc.3113A>G (p.Asp1038Gly)
c.872A>G (p.Asp291Gly)
c.1043A>G (p.Asp348Gly)
c.3158A>G (p.Asp1053Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.26475372T>GCA346109821OTOFc.3113A>C (p.Asp1038Ala)
c.872A>C (p.Asp291Ala)
c.1043A>C (p.Asp348Ala)
c.3158A>C (p.Asp1053Ala)
2g.26475372T=CA1239827076OTOFc.3113A= (p.Asp1038=)
c.872A= (p.Asp291=)
c.1043A= (p.Asp348=)
c.3158A= (p.Asp1053=)
2g.26475373C>ACA346109827OTOFc.3112G>T (p.Asp1038Tyr)
c.871G>T (p.Asp291Tyr)
c.1042G>T (p.Asp348Tyr)
c.3157G>T (p.Asp1053Tyr)
gnomAD v4
2g.26475373C>GCA346109831OTOFc.3112G>C (p.Asp1038His)
c.871G>C (p.Asp291His)
c.1042G>C (p.Asp348His)
c.3157G>C (p.Asp1053His)

Number of alleles fetched