Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.240878694_240878695delinsGCCA1339336107AGXTc.1072-20_1072-19delinsGC (p.=)
n.850-20_850-19delinsGC
2g.240878697delCA540538853AGXTc.1072-17del (p.=)
n.850-17del
dbSNP gnomAD
2g.240878697C=CA1339336108AGXTc.1072-17C= (p.=)
n.850-17C=
2g.240878697C>TCA2209408AGXTc.1072-17C>T (p.=)
n.850-17C>T
dbSNP ExAC gnomAD
2g.240878698G>ACA2209409AGXTc.1072-16G>A (p.=)
n.850-16G>A
dbSNP ExAC gnomAD
2g.240878698G>CCA766958890AGXTc.1072-16G>C (p.=)
n.850-16G>C
2g.240878698G=CA1339336109AGXTc.1072-16G= (p.=)
n.850-16G=
2g.240878698G>TCA540538857AGXTc.1072-16G>T (p.=)
n.850-16G>T
gnomAD
2g.240878701C=CA1339336110AGXTc.1072-13C= (p.=)
n.850-13C=
2g.240878701C>TCA540538860AGXTc.1072-13C>T (p.=)
n.850-13C>T
gnomAD
2g.240878705G>ACA915941797AGXTc.1072-9G>A (p.=)
n.850-9G>A
ClinVar
2g.240878705G=CA1339336111AGXTc.1072-9G= (p.=)
n.850-9G=
2g.240878711dupCA540538862AGXTc.1072-3dup (p.=)
n.850-3dup
dbSNP gnomAD
2g.240878707C>ACA1339336112AGXTc.1072-7C>A (p.=)
n.850-7C>A
2g.240878707C=CA1339336113AGXTc.1072-7C= (p.=)
n.850-7C=
2g.240878709C=CA1339336114AGXTc.1072-5C= (p.=)
n.850-5C=
2g.240878709C>GCA540538864AGXTc.1072-5C>G (p.=)
n.850-5C>G
gnomAD
2g.240878710C>ACA540538866AGXTc.1072-4C>A (p.=)
n.850-4C>A
gnomAD
2g.240878710C=CA1339336115AGXTc.1072-4C= (p.=)
n.850-4C=
2g.240878710C>TCA2209410AGXTc.1072-4C>T (p.=)
n.850-4C>T
ClinVar dbSNP ExAC gnomAD
2g.240878711C>ACA2209411AGXTc.1072-3C>A (p.=)
n.850-3C>A
dbSNP ExAC gnomAD
2g.240878711C=CA1339336116AGXTc.1072-3C= (p.=)
n.850-3C=
2g.240878711C>TCA540538868AGXTc.1072-3C>T (p.=)
n.850-3C>T
gnomAD
2g.240878712A>CCA351319714AGXTc.1072-2A>C (p.=)
n.850-2A>C
2g.240878712A>GCA351319715AGXTc.1072-2A>G (p.=)
n.850-2A>G
2g.240878712A>TCA351319716AGXTc.1072-2A>T (p.=)
n.850-2A>T
2g.240878713G>ACA351319717AGXTc.1072-1G>A (p.=)
n.850-1G>A
2g.240878713G>CCA351319719AGXTc.1072-1G>C (p.=)
n.850-1G>C
2g.240878713G>TCA351319718AGXTc.1072-1G>T (p.=)
n.850-1G>T
2g.240878714G>ACA2209412AGXTc.1072G>A (p.Val358Met)
n.850G>A
dbSNP ExAC gnomAD
2g.240878714G>CCA351319720AGXTc.1072G>C (p.Val358Leu)
n.850G>C
2g.240878714G=CA1339336117AGXTc.1072G= (p.Val358=)
n.850G=
2g.240878714G>TCA68181063AGXTc.1072G>T (p.Val358Leu)
n.850G>T
dbSNP
2g.240878715T>ACA351319721AGXTc.1073T>A (p.Val358Glu)
n.851T>A
2g.240878715T>CCA351319722AGXTc.1073T>C (p.Val358Ala)
n.851T>C
2g.240878715T>GCA351319723AGXTc.1073T>G (p.Val358Gly)
n.851T>G
2g.240878716G>ACA432026906AGXTc.1074G>A (p.Val358=)
n.852G>A
2g.240878716G>CCA432026907AGXTc.1074G>C (p.Val358=)
n.852G>C
2g.240878716G>TCA432026908AGXTc.1074G>T (p.Val358=)
n.852G>T
2g.240878717C>ACA351319724AGXTc.1075C>A (p.Leu359Met)
n.853C>A
2g.240878717C>GCA351319725AGXTc.1075C>G (p.Leu359Val)
n.853C>G
2g.240878717C>TCA432026917AGXTc.1075C>T (p.Leu359=)
n.853C>T
2g.240878718T>ACA351319726AGXTc.1076T>A (p.Leu359Gln)
n.854T>A
2g.240878718T>CCA275781AGXTc.1076T>C (p.Leu359Pro)
n.854T>C
ClinVar dbSNP
2g.240878718T>GCA351319727AGXTc.1076T>G (p.Leu359Arg)
n.854T>G
2g.240878718T=CA1339336118AGXTc.1076T= (p.Leu359=)
n.854T=
2g.240878719G>ACA2209413AGXTc.1077G>A (p.Leu359=)
n.855G>A
dbSNP ExAC gnomAD
2g.240878719G>CCA432026926AGXTc.1077G>C (p.Leu359=)
n.855G>C
2g.240878719G=CA1339336119AGXTc.1077G= (p.Leu359=)
n.855G=
2g.240878719G>TCA432026928AGXTc.1077G>T (p.Leu359=)
n.855G>T

Number of alleles fetched