Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.91297354_91297446delCA2626129391CCDC88Cc.3829_3921del (p.Ala1277_His1307del)
c.3721_3813del (p.Ala1241_His1271del)
n.3957_4049del
c.910_1002del (p.Ala304_His334del)
n.3955_4047del
gnomAD v4
14g.91297375_91297388delCA2626129430CCDC88Cc.3884_3897del (p.Arg1295LeufsTer23)
c.3776_3789del (p.Arg1259LeufsTer23)
n.4012_4025del
c.965_978del (p.Arg322LeufsTer23)
n.4010_4023del
gnomAD v4
14g.91297376G>ACA7309192CCDC88Cc.3895C>T (p.Arg1299Cys)
c.3787C>T (p.Arg1263Cys)
n.4023C>T
c.976C>T (p.Arg326Cys)
n.4021C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
14g.91297376G>CCA390618260CCDC88Cc.3895C>G (p.Arg1299Gly)
c.3787C>G (p.Arg1263Gly)
n.4023C>G
c.976C>G (p.Arg326Gly)
n.4021C>G
14g.91297376G=CA2154888614CCDC88Cc.3895C= (p.Arg1299=)
c.3787C= (p.Arg1263=)
n.4023C=
c.976C= (p.Arg326=)
n.4021C=
14g.91297376G>TCA390618261CCDC88Cc.3895C>A (p.Arg1299Ser)
c.3787C>A (p.Arg1263Ser)
n.4023C>A
c.976C>A (p.Arg326Ser)
n.4021C>A
gnomAD v4
14g.91297377G>ACA487547103CCDC88Cc.3894C>T (p.Ala1298=)
c.3786C>T (p.Ala1262=)
n.4022C>T
c.975C>T (p.Ala325=)
n.4020C>T
14g.91297377G>CCA487547105CCDC88Cc.3894C>G (p.Ala1298=)
c.3786C>G (p.Ala1262=)
n.4022C>G
c.975C>G (p.Ala325=)
n.4020C>G
14g.91297377G>TCA487547107CCDC88Cc.3894C>A (p.Ala1298=)
c.3786C>A (p.Ala1262=)
n.4022C>A
c.975C>A (p.Ala325=)
n.4020C>A
14g.91297378G>ACA390618265CCDC88Cc.3893C>T (p.Ala1298Val)
c.3785C>T (p.Ala1262Val)
n.4021C>T
c.974C>T (p.Ala325Val)
n.4019C>T
ClinVar dbSNP gnomAD v4
14g.91297378G>CCA7309193CCDC88Cc.3893C>G (p.Ala1298Gly)
c.3785C>G (p.Ala1262Gly)
n.4021C>G
c.974C>G (p.Ala325Gly)
n.4019C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.91297378G=CA2154888619CCDC88Cc.3893C= (p.Ala1298=)
c.3785C= (p.Ala1262=)
n.4021C=
c.974C= (p.Ala325=)
n.4019C=
14g.91297378G>TCA390618264CCDC88Cc.3893C>A (p.Ala1298Asp)
c.3785C>A (p.Ala1262Asp)
n.4021C>A
c.974C>A (p.Ala325Asp)
n.4019C>A
14g.91297379C>ACA390618267CCDC88Cc.3892G>T (p.Ala1298Ser)
c.3784G>T (p.Ala1262Ser)
n.4020G>T
c.973G>T (p.Ala325Ser)
n.4018G>T
14g.91297379C>GCA390618269CCDC88Cc.3892G>C (p.Ala1298Pro)
c.3784G>C (p.Ala1262Pro)
n.4020G>C
c.973G>C (p.Ala325Pro)
n.4018G>C
14g.91297379C>TCA390618271CCDC88Cc.3892G>A (p.Ala1298Thr)
c.3784G>A (p.Ala1262Thr)
n.4020G>A
c.973G>A (p.Ala325Thr)
n.4018G>A
gnomAD v4
14g.91297380C>ACA390618273CCDC88Cc.3891G>T (p.Gln1297His)
c.3783G>T (p.Gln1261His)
n.4019G>T
c.972G>T (p.Gln324His)
n.4017G>T
14g.91297380C>GCA390618275CCDC88Cc.3891G>C (p.Gln1297His)
c.3783G>C (p.Gln1261His)
n.4019G>C
c.972G>C (p.Gln324His)
n.4017G>C
14g.91297380C>TCA487547117CCDC88Cc.3891G>A (p.Gln1297=)
c.3783G>A (p.Gln1261=)
n.4019G>A
c.972G>A (p.Gln324=)
n.4017G>A
14g.91297381T>ACA390618281CCDC88Cc.3890A>T (p.Gln1297Leu)
c.3782A>T (p.Gln1261Leu)
n.4018A>T
c.971A>T (p.Gln324Leu)
n.4016A>T
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.91297381T>CCA390618280CCDC88Cc.3890A>G (p.Gln1297Arg)
c.3782A>G (p.Gln1261Arg)
n.4018A>G
c.971A>G (p.Gln324Arg)
n.4016A>G
COSMIC COSMIC
14g.91297381T>GCA390618277CCDC88Cc.3890A>C (p.Gln1297Pro)
c.3782A>C (p.Gln1261Pro)
n.4018A>C
c.971A>C (p.Gln324Pro)
n.4016A>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.91297381T=CA2154888630CCDC88Cc.3890A= (p.Gln1297=)
c.3782A= (p.Gln1261=)
n.4018A=
c.971A= (p.Gln324=)
n.4016A=
14g.91297382G>ACA390618284CCDC88Cc.3889C>T (p.Gln1297Ter)
c.3781C>T (p.Gln1261Ter)
n.4017C>T
c.970C>T (p.Gln324Ter)
n.4015C>T
dbSNP gnomAD v2
14g.91297382G>CCA390618285CCDC88Cc.3889C>G (p.Gln1297Glu)
c.3781C>G (p.Gln1261Glu)
n.4017C>G
c.970C>G (p.Gln324Glu)
n.4015C>G
14g.91297382G=CA2154888637CCDC88Cc.3889C= (p.Gln1297=)
c.3781C= (p.Gln1261=)
n.4017C=
c.970C= (p.Gln324=)
n.4015C=
14g.91297382G>TCA390618287CCDC88Cc.3889C>A (p.Gln1297Lys)
c.3781C>A (p.Gln1261Lys)
n.4017C>A
c.970C>A (p.Gln324Lys)
n.4015C>A
14g.91297383C>ACA390618289CCDC88Cc.3888G>T (p.Trp1296Cys)
c.3780G>T (p.Trp1260Cys)
n.4016G>T
c.969G>T (p.Trp323Cys)
n.4014G>T
14g.91297383C>GCA390618290CCDC88Cc.3888G>C (p.Trp1296Cys)
c.3780G>C (p.Trp1260Cys)
n.4016G>C
c.969G>C (p.Trp323Cys)
n.4014G>C
14g.91297383C>TCA390618291CCDC88Cc.3888G>A (p.Trp1296Ter)
c.3780G>A (p.Trp1260Ter)
n.4016G>A
c.969G>A (p.Trp323Ter)
n.4014G>A
14g.91297384C>ACA390618292CCDC88Cc.3887G>T (p.Trp1296Leu)
c.3779G>T (p.Trp1260Leu)
n.4015G>T
c.968G>T (p.Trp323Leu)
n.4013G>T
14g.91297384C>GCA390618294CCDC88Cc.3887G>C (p.Trp1296Ser)
c.3779G>C (p.Trp1260Ser)
n.4015G>C
c.968G>C (p.Trp323Ser)
n.4013G>C
14g.91297384C>TCA390618293CCDC88Cc.3887G>A (p.Trp1296Ter)
c.3779G>A (p.Trp1260Ter)
n.4015G>A
c.968G>A (p.Trp323Ter)
n.4013G>A
14g.91297385A=CA2154888644CCDC88Cc.3886T= (p.Trp1296=)
c.3778T= (p.Trp1260=)
n.4014T=
c.967T= (p.Trp323=)
n.4012T=
14g.91297385A>CCA390618295CCDC88Cc.3886T>G (p.Trp1296Gly)
c.3778T>G (p.Trp1260Gly)
n.4014T>G
c.967T>G (p.Trp323Gly)
n.4012T>G
14g.91297385A>GCA390618297CCDC88Cc.3886T>C (p.Trp1296Arg)
c.3778T>C (p.Trp1260Arg)
n.4014T>C
c.967T>C (p.Trp323Arg)
n.4012T>C
dbSNP gnomAD v3 gnomAD v4
14g.91297385A>TCA390618298CCDC88Cc.3886T>A (p.Trp1296Arg)
c.3778T>A (p.Trp1260Arg)
n.4014T>A
c.967T>A (p.Trp323Arg)
n.4012T>A
14g.91297386G>ACA487547141CCDC88Cc.3885C>T (p.Arg1295=)
c.3777C>T (p.Arg1259=)
n.4013C>T
c.966C>T (p.Arg322=)
n.4011C>T
14g.91297386G>CCA487547145CCDC88Cc.3885C>G (p.Arg1295=)
c.3777C>G (p.Arg1259=)
n.4013C>G
c.966C>G (p.Arg322=)
n.4011C>G
14g.91297386G>TCA487547147CCDC88Cc.3885C>A (p.Arg1295=)
c.3777C>A (p.Arg1259=)
n.4013C>A
c.966C>A (p.Arg322=)
n.4011C>A
14g.91297387C>ACA390618301CCDC88Cc.3884G>T (p.Arg1295Leu)
c.3776G>T (p.Arg1259Leu)
n.4012G>T
c.965G>T (p.Arg322Leu)
n.4010G>T
dbSNP gnomAD v2 gnomAD v4
14g.91297387C=CA2154888653CCDC88Cc.3884G= (p.Arg1295=)
c.3776G= (p.Arg1259=)
n.4012G=
c.965G= (p.Arg322=)
n.4010G=
14g.91297387C>GCA390618303CCDC88Cc.3884G>C (p.Arg1295Pro)
c.3776G>C (p.Arg1259Pro)
n.4012G>C
c.965G>C (p.Arg322Pro)
n.4010G>C
dbSNP gnomAD v2 gnomAD v4
14g.91297387C>TCA390618304CCDC88Cc.3884G>A (p.Arg1295His)
c.3776G>A (p.Arg1259His)
n.4012G>A
c.965G>A (p.Arg322His)
n.4010G>A
dbSNP gnomAD v2 gnomAD v4
14g.91297388G>ACA7309194CCDC88Cc.3883C>T (p.Arg1295Cys)
c.3775C>T (p.Arg1259Cys)
n.4011C>T
c.964C>T (p.Arg322Cys)
n.4009C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.91297388G>CCA390618307CCDC88Cc.3883C>G (p.Arg1295Gly)
c.3775C>G (p.Arg1259Gly)
n.4011C>G
c.964C>G (p.Arg322Gly)
n.4009C>G
dbSNP
14g.91297388G=CA2154888656CCDC88Cc.3883C= (p.Arg1295=)
c.3775C= (p.Arg1259=)
n.4011C=
c.964C= (p.Arg322=)
n.4009C=
14g.91297388G>TCA390618308CCDC88Cc.3883C>A (p.Arg1295Ser)
c.3775C>A (p.Arg1259Ser)
n.4011C>A
c.964C>A (p.Arg322Ser)
n.4009C>A
gnomAD v4
14g.91297389G>ACA487547161CCDC88Cc.3882C>T (p.Asn1294=)
c.3774C>T (p.Asn1258=)
n.4010C>T
c.963C>T (p.Asn321=)
n.4008C>T
ClinVar dbSNP
14g.91297389G>CCA390618310CCDC88Cc.3882C>G (p.Asn1294Lys)
c.3774C>G (p.Asn1258Lys)
n.4010C>G
c.963C>G (p.Asn321Lys)
n.4008C>G

Number of alleles fetched