Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.44148538_44152555dupCA1139771162GCKc.*207-130_*678-705dup
c.209-130_680-705dup
n.695-130_2387dup
c.212-130_683-705dup
c.206-130_677-705dup
c.209-130_629-705dup
7g.44152388A>CCA454610305GCKc.*244T>G (n.*244T>G)
c.246T>G (p.Thr82=)
n.732T>G
c.249T>G (p.Thr83=)
c.243T>G (p.Thr81=)
gnomAD v4
7g.44152388A>GCA454610307GCKc.*244T>C (n.*244T>C)
c.246T>C (p.Thr82=)
n.732T>C
c.249T>C (p.Thr83=)
c.243T>C (p.Thr81=)
7g.44152388A>TCA454610306GCKc.*244T>A (n.*244T>A)
c.246T>A (p.Thr82=)
n.732T>A
c.249T>A (p.Thr83=)
c.243T>A (p.Thr81=)
7g.44152389G>ACA367402995GCKc.*243C>T (n.*243C>T)
c.245C>T (p.Thr82Ile)
n.731C>T
c.248C>T (p.Thr83Ile)
c.242C>T (p.Thr81Ile)
ClinVar
7g.44152389G>CCA367402997GCKc.*243C>G (n.*243C>G)
c.245C>G (p.Thr82Ser)
n.731C>G
c.248C>G (p.Thr83Ser)
c.242C>G (p.Thr81Ser)
7g.44152389G>TCA367402998GCKc.*243C>A (n.*243C>A)
c.245C>A (p.Thr82Asn)
n.731C>A
c.248C>A (p.Thr83Asn)
c.242C>A (p.Thr81Asn)
7g.44152390T>ACA367403000GCKc.*242A>T (n.*242A>T)
c.244A>T (p.Thr82Ser)
n.730A>T
c.247A>T (p.Thr83Ser)
c.241A>T (p.Thr81Ser)
7g.44152390T>CCA367403002GCKc.*242A>G (n.*242A>G)
c.244A>G (p.Thr82Ala)
n.730A>G
c.247A>G (p.Thr83Ala)
c.241A>G (p.Thr81Ala)
7g.44152390T>GCA367403003GCKc.*242A>C (n.*242A>C)
c.244A>C (p.Thr82Pro)
n.730A>C
c.247A>C (p.Thr83Pro)
c.241A>C (p.Thr81Pro)
7g.44152391G>ACA454610309GCKc.*241C>T (n.*241C>T)
c.243C>T (p.Gly81=)
n.729C>T
c.246C>T (p.Gly82=)
c.240C>T (p.Gly80=)
7g.44152391G>CCA454610310GCKc.*241C>G (n.*241C>G)
c.243C>G (p.Gly81=)
n.729C>G
c.246C>G (p.Gly82=)
c.240C>G (p.Gly80=)
7g.44152391G>TCA454610312GCKc.*241C>A (n.*241C>A)
c.243C>A (p.Gly81=)
n.729C>A
c.246C>A (p.Gly82=)
c.240C>A (p.Gly80=)
7g.44152392C>ACA367403008GCKc.*240G>T (n.*240G>T)
c.242G>T (p.Gly81Val)
n.728G>T
c.245G>T (p.Gly82Val)
c.239G>T (p.Gly80Val)
7g.44152392C=CA1703637072GCKc.*240G= (n.*240G=)
c.242G= (p.Gly81=)
n.728G=
c.245G= (p.Gly82=)
c.239G= (p.Gly80=)
7g.44152392C>GCA367403006GCKc.*240G>C (n.*240G>C)
c.242G>C (p.Gly81Ala)
n.728G>C
c.245G>C (p.Gly82Ala)
c.239G>C (p.Gly80Ala)
7g.44152392C>TCA157919284GCKc.*240G>A (n.*240G>A)
c.242G>A (p.Gly81Asp)
n.728G>A
c.245G>A (p.Gly82Asp)
c.239G>A (p.Gly80Asp)
dbSNP
7g.44152393C>ACA367403010GCKc.*239G>T (n.*239G>T)
c.241G>T (p.Gly81Cys)
n.727G>T
c.244G>T (p.Gly82Cys)
c.238G>T (p.Gly80Cys)
7g.44152393C>GCA367403013GCKc.*239G>C (n.*239G>C)
c.241G>C (p.Gly81Arg)
n.727G>C
c.244G>C (p.Gly82Arg)
c.238G>C (p.Gly80Arg)
7g.44152393C>TCA367403011GCKc.*239G>A (n.*239G>A)
c.241G>A (p.Gly81Ser)
n.727G>A
c.244G>A (p.Gly82Ser)
c.238G>A (p.Gly80Ser)
7g.44152394A>CCA454610315GCKc.*238T>G (n.*238T>G)
c.240T>G (p.Gly80=)
n.726T>G
c.243T>G (p.Gly81=)
c.237T>G (p.Gly79=)
7g.44152394A>GCA454610316GCKc.*238T>C (n.*238T>C)
c.240T>C (p.Gly80=)
n.726T>C
c.243T>C (p.Gly81=)
c.237T>C (p.Gly79=)
7g.44152394A>TCA454610317GCKc.*238T>A (n.*238T>A)
c.240T>A (p.Gly80=)
n.726T>A
c.243T>A (p.Gly81=)
c.237T>A (p.Gly79=)
7g.44152395C>ACA367403015GCKc.*237G>T (n.*237G>T)
c.239G>T (p.Gly80Val)
n.725G>T
c.242G>T (p.Gly81Val)
c.236G>T (p.Gly79Val)
COSMIC COSMIC
7g.44152395C>GCA367403019GCKc.*237G>C (n.*237G>C)
c.239G>C (p.Gly80Ala)
n.725G>C
c.242G>C (p.Gly81Ala)
c.236G>C (p.Gly79Ala)
7g.44152395C>TCA367403017GCKc.*237G>A (n.*237G>A)
c.239G>A (p.Gly80Asp)
n.725G>A
c.242G>A (p.Gly81Asp)
c.236G>A (p.Gly79Asp)
7g.44152396C>ACA367403020GCKc.*236G>T (n.*236G>T)
c.238G>T (p.Gly80Cys)
n.724G>T
c.241G>T (p.Gly81Cys)
c.235G>T (p.Gly79Cys)
7g.44152396C=CA1703637073GCKc.*236G= (n.*236G=)
c.238G= (p.Gly80=)
n.724G=
c.241G= (p.Gly81=)
c.235G= (p.Gly79=)
7g.44152396C>GCA367403022GCKc.*236G>C (n.*236G>C)
c.238G>C (p.Gly80Arg)
n.724G>C
c.241G>C (p.Gly81Arg)
c.235G>C (p.Gly79Arg)
7g.44152396C>TCA367403023GCKc.*236G>A (n.*236G>A)
c.238G>A (p.Gly80Ser)
n.724G>A
c.241G>A (p.Gly81Ser)
c.235G>A (p.Gly79Ser)
ClinVar dbSNP
7g.44152397C>ACA454610325GCKc.*235G>T (n.*235G>T)
c.237G>T (p.Leu79=)
n.723G>T
c.240G>T (p.Leu80=)
c.234G>T (p.Leu78=)
7g.44152397C=CA1703637074GCKc.*235G= (n.*235G=)
c.237G= (p.Leu79=)
n.723G=
c.240G= (p.Leu80=)
c.234G= (p.Leu78=)
7g.44152397C>GCA4239685GCKc.*235G>C (n.*235G>C)
c.237G>C (p.Leu79=)
n.723G>C
c.240G>C (p.Leu80=)
c.234G>C (p.Leu78=)
dbSNP ExAC gnomAD v2 COSMIC COSMIC
7g.44152397C>TCA4239686GCKc.*235G>A (n.*235G>A)
c.237G>A (p.Leu79=)
n.723G>A
c.240G>A (p.Leu80=)
c.234G>A (p.Leu78=)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.44152398A>CCA367403026GCKc.*234T>G (n.*234T>G)
c.236T>G (p.Leu79Arg)
n.722T>G
c.239T>G (p.Leu80Arg)
c.233T>G (p.Leu78Arg)
7g.44152398A>GCA367403028GCKc.*234T>C (n.*234T>C)
c.236T>C (p.Leu79Pro)
n.722T>C
c.239T>C (p.Leu80Pro)
c.233T>C (p.Leu78Pro)
7g.44152398A>TCA367403030GCKc.*234T>A (n.*234T>A)
c.236T>A (p.Leu79Gln)
n.722T>A
c.239T>A (p.Leu80Gln)
c.233T>A (p.Leu78Gln)
7g.44152399G>ACA454610327GCKc.*233C>T (n.*233C>T)
c.235C>T (p.Leu79=)
n.721C>T
c.238C>T (p.Leu80=)
c.232C>T (p.Leu78=)
7g.44152399G>CCA367403031GCKc.*233C>G (n.*233C>G)
c.235C>G (p.Leu79Val)
n.721C>G
c.238C>G (p.Leu80Val)
c.232C>G (p.Leu78Val)
7g.44152399G>TCA367403033GCKc.*233C>A (n.*233C>A)
c.235C>A (p.Leu79Met)
n.721C>A
c.238C>A (p.Leu80Met)
c.232C>A (p.Leu78Met)
7g.44152400G>ACA454610329GCKc.*232C>T (n.*232C>T)
c.234C>T (p.Asp78=)
n.720C>T
c.237C>T (p.Asp79=)
c.231C>T (p.Asp77=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.44152400G>CCA367403035GCKc.*232C>G (n.*232C>G)
c.234C>G (p.Asp78Glu)
n.720C>G
c.237C>G (p.Asp79Glu)
c.231C>G (p.Asp77Glu)
7g.44152400G=CA1703637075GCKc.*232C= (n.*232C=)
c.234C= (p.Asp78=)
n.720C=
c.237C= (p.Asp79=)
c.231C= (p.Asp77=)
7g.44152400G>TCA367403036GCKc.*232C>A (n.*232C>A)
c.234C>A (p.Asp78Glu)
n.720C>A
c.237C>A (p.Asp79Glu)
c.231C>A (p.Asp77Glu)
ClinVar
7g.44152401T>ACA367403039GCKc.*231A>T (n.*231A>T)
c.233A>T (p.Asp78Val)
n.719A>T
c.236A>T (p.Asp79Val)
c.230A>T (p.Asp77Val)
7g.44152401T>CCA367403041GCKc.*231A>G (n.*231A>G)
c.233A>G (p.Asp78Gly)
n.719A>G
c.236A>G (p.Asp79Gly)
c.230A>G (p.Asp77Gly)
7g.44152401T>GCA367403040GCKc.*231A>C (n.*231A>C)
c.233A>C (p.Asp78Ala)
n.719A>C
c.236A>C (p.Asp79Ala)
c.230A>C (p.Asp77Ala)
7g.44152402C>ACA367403044GCKc.*230G>T (n.*230G>T)
c.232G>T (p.Asp78Tyr)
n.718G>T
c.235G>T (p.Asp79Tyr)
c.229G>T (p.Asp77Tyr)
ClinVar
7g.44152402C>GCA367403045GCKc.*230G>C (n.*230G>C)
c.232G>C (p.Asp78His)
n.718G>C
c.235G>C (p.Asp79His)
c.229G>C (p.Asp77His)
7g.44152402C>TCA367403047GCKc.*230G>A (n.*230G>A)
c.232G>A (p.Asp78Asn)
n.718G>A
c.235G>A (p.Asp79Asn)
c.229G>A (p.Asp77Asn)

Number of alleles fetched