Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.110780846_110780907delCA335579RBM20c.237_298del (p.Asn80ProfsTer?)
c.-148_-87del (n.-148_-87del)
c.72_133del (p.Asn25ProfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.110780861_110780864delCA213234514RBM20c.252_255del (p.Ser85LeufsTer18)
c.-133_-130del (n.-133_-130del)
c.87_90del (p.Ser30LeufsTer18)
dbSNP
10g.110780862_110780865delCA378379211RBM20c.253_256del (p.Ser85LeufsTer18)
c.-132_-129del (n.-132_-129del)
c.88_91del (p.Ser30LeufsTer18)
10g.110780864A>CCA333148RBM20c.255A>C (p.Ser85=)
c.-130A>C (n.-130A>C)
c.90A>C (p.Ser30=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.110780864A>GCA471506585RBM20c.255A>G (p.Ser85=)
c.-130A>G (n.-130A>G)
c.90A>G (p.Ser30=)
10g.110780864A>TCA471506586RBM20c.255A>T (p.Ser85=)
c.-130A>T (n.-130A>T)
c.90A>T (p.Ser30=)
10g.110780865C>ACA378379222RBM20c.256C>A (p.Pro86Thr)
c.-129C>A (n.-129C>A)
c.91C>A (p.Pro31Thr)
10g.110780865C>GCA378379223RBM20c.256C>G (p.Pro86Ala)
c.-129C>G (n.-129C>G)
c.91C>G (p.Pro31Ala)
10g.110780865C>TCA378379226RBM20c.256C>T (p.Pro86Ser)
c.-129C>T (n.-129C>T)
c.91C>T (p.Pro31Ser)
dbSNP gnomAD v2 gnomAD v4
10g.110780866C>ACA378379234RBM20c.257C>A (p.Pro86His)
c.-128C>A (n.-128C>A)
c.92C>A (p.Pro31His)
gnomAD v4
10g.110780866C>GCA378379233RBM20c.257C>G (p.Pro86Arg)
c.-128C>G (n.-128C>G)
c.92C>G (p.Pro31Arg)
10g.110780866C>TCA378379231RBM20c.257C>T (p.Pro86Leu)
c.-128C>T (n.-128C>T)
c.92C>T (p.Pro31Leu)
ClinVar dbSNP gnomAD v4
10g.110780867T>ACA471506589RBM20c.258T>A (p.Pro86=)
c.-127T>A (n.-127T>A)
c.93T>A (p.Pro31=)
gnomAD v4
10g.110780867T>CCA471506590RBM20c.258T>C (p.Pro86=)
c.-127T>C (n.-127T>C)
c.93T>C (p.Pro31=)
10g.110780867T>GCA471506591RBM20c.258T>G (p.Pro86=)
c.-127T>G (n.-127T>G)
c.93T>G (p.Pro31=)
ClinVar dbSNP
10g.110780868G>ACA378379238RBM20c.259G>A (p.Ala87Thr)
c.-126G>A (n.-126G>A)
c.94G>A (p.Ala32Thr)
ClinVar gnomAD v4
10g.110780868G>CCA378379241RBM20c.259G>C (p.Ala87Pro)
c.-126G>C (n.-126G>C)
c.94G>C (p.Ala32Pro)
10g.110780868G>TCA378379242RBM20c.259G>T (p.Ala87Ser)
c.-126G>T (n.-126G>T)
c.94G>T (p.Ala32Ser)
10g.110780869C>ACA378379245RBM20c.260C>A (p.Ala87Asp)
c.-125C>A (n.-125C>A)
c.95C>A (p.Ala32Asp)
gnomAD v4
10g.110780869C>GCA378379248RBM20c.260C>G (p.Ala87Gly)
c.-125C>G (n.-125C>G)
c.95C>G (p.Ala32Gly)
10g.110780869C>TCA378379251RBM20c.260C>T (p.Ala87Val)
c.-125C>T (n.-125C>T)
c.95C>T (p.Ala32Val)
ClinVar dbSNP
10g.110780870C>ACA471506595RBM20c.261C>A (p.Ala87=)
c.-124C>A (n.-124C>A)
c.96C>A (p.Ala32=)
10g.110780870C>GCA471506596RBM20c.261C>G (p.Ala87=)
c.-124C>G (n.-124C>G)
c.96C>G (p.Ala32=)
gnomAD v4
10g.110780870C>TCA10587074RBM20c.261C>T (p.Ala87=)
c.-124C>T (n.-124C>T)
c.96C>T (p.Ala32=)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.110780871A>CCA378379255RBM20c.262A>C (p.Ser88Arg)
c.-123A>C (n.-123A>C)
c.97A>C (p.Ser33Arg)
10g.110780871A>GCA378379257RBM20c.262A>G (p.Ser88Gly)
c.-123A>G (n.-123A>G)
c.97A>G (p.Ser33Gly)
ClinVar dbSNP gnomAD v4
10g.110780871A>TCA378379260RBM20c.262A>T (p.Ser88Cys)
c.-123A>T (n.-123A>T)
c.97A>T (p.Ser33Cys)
10g.110780872G>ACA378379263RBM20c.263G>A (p.Ser88Asn)
c.-122G>A (n.-122G>A)
c.98G>A (p.Ser33Asn)
dbSNP gnomAD v2
10g.110780872G>CCA378379265RBM20c.263G>C (p.Ser88Thr)
c.-122G>C (n.-122G>C)
c.98G>C (p.Ser33Thr)
10g.110780872G>TCA378379267RBM20c.263G>T (p.Ser88Ile)
c.-122G>T (n.-122G>T)
c.98G>T (p.Ser33Ile)
10g.110780873T>ACA378379273RBM20c.264T>A (p.Ser88Arg)
c.-121T>A (n.-121T>A)
c.99T>A (p.Ser33Arg)
10g.110780873T>CCA471506600RBM20c.264T>C (p.Ser88=)
c.-121T>C (n.-121T>C)
c.99T>C (p.Ser33=)
gnomAD v4
10g.110780873T>GCA378379270RBM20c.264T>G (p.Ser88Arg)
c.-121T>G (n.-121T>G)
c.99T>G (p.Ser33Arg)
10g.110780874C>ACA378379276RBM20c.265C>A (p.Leu89Ile)
c.-120C>A (n.-120C>A)
c.100C>A (p.Leu34Ile)
10g.110780874C>GCA378379277RBM20c.265C>G (p.Leu89Val)
c.-120C>G (n.-120C>G)
c.100C>G (p.Leu34Val)
10g.110780874C>TCA378379279RBM20c.265C>T (p.Leu89Phe)
c.-120C>T (n.-120C>T)
c.100C>T (p.Leu34Phe)
10g.110780875T>ACA378379282RBM20c.266T>A (p.Leu89His)
c.-119T>A (n.-119T>A)
c.101T>A (p.Leu34His)
10g.110780875T>CCA378379284RBM20c.266T>C (p.Leu89Pro)
c.-119T>C (n.-119T>C)
c.101T>C (p.Leu34Pro)
gnomAD v4 COSMIC
10g.110780875T>GCA378379287RBM20c.266T>G (p.Leu89Arg)
c.-119T>G (n.-119T>G)
c.101T>G (p.Leu34Arg)
10g.110780876C>ACA471506603RBM20c.267C>A (p.Leu89=)
c.-118C>A (n.-118C>A)
c.102C>A (p.Leu34=)
10g.110780876C>GCA471506604RBM20c.267C>G (p.Leu89=)
c.-118C>G (n.-118C>G)
c.102C>G (p.Leu34=)
10g.110780876C>TCA471506605RBM20c.267C>T (p.Leu89=)
c.-118C>T (n.-118C>T)
c.102C>T (p.Leu34=)
10g.110780877C>ACA378379290RBM20c.268C>A (p.Gln90Lys)
c.-117C>A (n.-117C>A)
c.103C>A (p.Gln35Lys)
10g.110780877C>GCA378379292RBM20c.268C>G (p.Gln90Glu)
c.-117C>G (n.-117C>G)
c.103C>G (p.Gln35Glu)
10g.110780877C>TCA378379294RBM20c.268C>T (p.Gln90Ter)
c.-117C>T (n.-117C>T)
c.103C>T (p.Gln35Ter)
10g.110780878A>CCA378379298RBM20c.269A>C (p.Gln90Pro)
c.-116A>C (n.-116A>C)
c.104A>C (p.Gln35Pro)
10g.110780878A>GCA378379299RBM20c.269A>G (p.Gln90Arg)
c.-116A>G (n.-116A>G)
c.104A>G (p.Gln35Arg)
dbSNP gnomAD v3 gnomAD v4
10g.110780878A>TCA378379300RBM20c.269A>T (p.Gln90Leu)
c.-116A>T (n.-116A>T)
c.104A>T (p.Gln35Leu)
gnomAD v4
10g.110780879G>ACA471506609RBM20c.270G>A (p.Gln90=)
c.-115G>A (n.-115G>A)
c.105G>A (p.Gln35=)
dbSNP
10g.110780879G>CCA378379302RBM20c.270G>C (p.Gln90His)
c.-115G>C (n.-115G>C)
c.105G>C (p.Gln35His)

Number of alleles fetched