Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.47350166_47350170dupCA593487652RBP3c.1682_1686dup (p.Thr563GlyfsTer5)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.47350168G>ACA376671274RBP3c.1684G>A (p.Ala562Thr)
gnomAD v4
10g.47350168G>CCA376671272RBP3c.1684G>C (p.Ala562Pro)
10g.47350168G>TCA376671275RBP3c.1684G>T (p.Ala562Ser)
gnomAD v4
10g.47350169C>ACA376671278RBP3c.1685C>A (p.Ala562Asp)
10g.47350169C=CA1907806224RBP3c.1685C= (p.Ala562=)
10g.47350169C>GCA376671280RBP3c.1685C>G (p.Ala562Gly)
10g.47350169C>TCA376671279RBP3c.1685C>T (p.Ala562Val)
dbSNP gnomAD v3 gnomAD v4
10g.47350170C>ACA469782349RBP3c.1686C>A (p.Ala562=)
10g.47350170C>GCA469782348RBP3c.1686C>G (p.Ala562=)
10g.47350170C>TCA469782347RBP3c.1686C>T (p.Ala562=)
10g.47350171A>CCA376671283RBP3c.1687A>C (p.Thr563Pro)
10g.47350171A>GCA376671285RBP3c.1687A>G (p.Thr563Ala)
10g.47350171A>TCA376671284RBP3c.1687A>T (p.Thr563Ser)
10g.47350172C>ACA376671287RBP3c.1688C>A (p.Thr563Lys)
10g.47350172C=CA1907806226RBP3c.1688C= (p.Thr563=)
10g.47350172C>GCA376671289RBP3c.1688C>G (p.Thr563Arg)
10g.47350172C>TCA376671290RBP3c.1688C>T (p.Thr563Ile)
dbSNP gnomAD v2 gnomAD v4
10g.47350173A=CA1907806227RBP3c.1689A= (p.Thr563=)
10g.47350173A>CCA469782356RBP3c.1689A>C (p.Thr563=)
dbSNP gnomAD v4
10g.47350173A>GCA469782362RBP3c.1689A>G (p.Thr563=)
dbSNP
10g.47350173A>TCA469782364RBP3c.1689A>T (p.Thr563=)
10g.47350174C>ACA376671292RBP3c.1690C>A (p.Leu564Met)
10g.47350174C>GCA376671293RBP3c.1690C>G (p.Leu564Val)
10g.47350174C>TCA469782365RBP3c.1690C>T (p.Leu564=)
10g.47350175T>ACA376671295RBP3c.1691T>A (p.Leu564Gln)
10g.47350175T>CCA376671297RBP3c.1691T>C (p.Leu564Pro)
10g.47350175T>GCA376671298RBP3c.1691T>G (p.Leu564Arg)
10g.47350176G>ACA469782371RBP3c.1692G>A (p.Leu564=)
10g.47350176G>CCA469782372RBP3c.1692G>C (p.Leu564=)
10g.47350176G>TCA469782373RBP3c.1692G>T (p.Leu564=)
gnomAD v4
10g.47350177G>ACA376671300RBP3c.1693G>A (p.Val565Ile)
dbSNP gnomAD v3 gnomAD v4
10g.47350177G>CCA376671301RBP3c.1693G>C (p.Val565Leu)
10g.47350177G=CA1907806229RBP3c.1693G= (p.Val565=)
10g.47350177G>TCA376671303RBP3c.1693G>T (p.Val565Leu)
gnomAD v4
10g.47350178T>ACA376671305RBP3c.1694T>A (p.Val565Glu)
10g.47350178T>CCA5487461RBP3c.1694T>C (p.Val565Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.47350178T>GCA376671306RBP3c.1694T>G (p.Val565Gly)
10g.47350178T=CA1907806231RBP3c.1694T= (p.Val565=)
10g.47350179A=CA1907806233RBP3c.1695A= (p.Val565=)
10g.47350179A>CCA469782376RBP3c.1695A>C (p.Val565=)
10g.47350179A>GCA469782378RBP3c.1695A>G (p.Val565=)
gnomAD v4
10g.47350179A>TCA469782379RBP3c.1695A>T (p.Val565=)
dbSNP
10g.47350180G>ACA376671309RBP3c.1696G>A (p.Gly566Ser)
gnomAD v4
10g.47350180G>CCA376671310RBP3c.1696G>C (p.Gly566Arg)
10g.47350180G>TCA376671311RBP3c.1696G>T (p.Gly566Cys)
10g.47350181G>ACA376671313RBP3c.1697G>A (p.Gly566Asp)
gnomAD v4
10g.47350181G>CCA376671314RBP3c.1697G>C (p.Gly566Ala)
10g.47350181G>TCA376671315RBP3c.1697G>T (p.Gly566Val)
10g.47350182T>ACA469782389RBP3c.1698T>A (p.Gly566=)

Number of alleles fetched