Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.23203790A=CA2078579938SGCGc.96A= (p.Arg32=)
c.150A= (p.Arg50=)
13g.23203790A>CCA387502528SGCGc.96A>C (p.Arg32Ser)
c.150A>C (p.Arg50Ser)
13g.23203790A>GCA6909564SGCGc.96A>G (p.Arg32=)
c.150A>G (p.Arg50=)
dbSNP ExAC gnomAD v2 gnomAD v4
13g.23203790A>TCA387502525SGCGc.96A>T (p.Arg32Ser)
c.150A>T (p.Arg50Ser)
13g.23203791A>CCA387502529SGCGc.97A>C (p.Lys33Gln)
c.151A>C (p.Lys51Gln)
gnomAD v4
13g.23203791A>GCA387502531SGCGc.97A>G (p.Lys33Glu)
c.151A>G (p.Lys51Glu)
13g.23203791A>TCA387502533SGCGc.97A>T (p.Lys33Ter)
c.151A>T (p.Lys51Ter)
13g.23203792A=CA2078579939SGCGc.98A= (p.Lys33=)
c.152A= (p.Lys51=)
13g.23203792A>CCA6909565SGCGc.98A>C (p.Lys33Thr)
c.152A>C (p.Lys51Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
13g.23203792A>GCA6909566SGCGc.98A>G (p.Lys33Arg)
c.152A>G (p.Lys51Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
13g.23203792A>TCA387502537SGCGc.98A>T (p.Lys33Met)
c.152A>T (p.Lys51Met)
13g.23203793G>ACA6909567SGCGc.99G>A (p.Lys33=)
c.153G>A (p.Lys51=)
ClinVar dbSNP ExAC gnomAD v4
13g.23203793G>CCA387502539SGCGc.99G>C (p.Lys33Asn)
c.153G>C (p.Lys51Asn)
gnomAD v4
13g.23203793G=CA2078579940SGCGc.99G= (p.Lys33=)
c.153G= (p.Lys51=)
13g.23203793G>TCA387502541SGCGc.99G>T (p.Lys33Asn)
c.153G>T (p.Lys51Asn)
gnomAD v4
13g.23203794C>ACA387502543SGCGc.100C>A (p.Arg34Ser)
c.154C>A (p.Arg52Ser)
13g.23203794C=CA2078579941SGCGc.100C= (p.Arg34=)
c.154C= (p.Arg52=)
13g.23203794C>GCA387502546SGCGc.100C>G (p.Arg34Gly)
c.154C>G (p.Arg52Gly)
13g.23203794C>TCA6909568SGCGc.100C>T (p.Arg34Cys)
c.154C>T (p.Arg52Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
13g.23203795G>ACA6909569SGCGc.101G>A (p.Arg34His)
c.155G>A (p.Arg52His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
13g.23203795G>CCA387502551SGCGc.101G>C (p.Arg34Pro)
c.155G>C (p.Arg52Pro)
13g.23203795G=CA2078579942SGCGc.101G= (p.Arg34=)
c.155G= (p.Arg52=)
13g.23203795G>TCA246628974SGCGc.101G>T (p.Arg34Leu)
c.155G>T (p.Arg52Leu)
dbSNP
13g.23203796C>ACA6909571SGCGc.102C>A (p.Arg34=)
c.156C>A (p.Arg52=)
dbSNP ExAC
13g.23203796C=CA2078579943SGCGc.102C= (p.Arg34=)
c.156C= (p.Arg52=)
13g.23203796C>GCA482903177SGCGc.102C>G (p.Arg34=)
c.156C>G (p.Arg52=)
13g.23203796C>TCA6909570SGCGc.102C>T (p.Arg34=)
c.156C>T (p.Arg52=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.23203797T>ACA387502558SGCGc.103T>A (p.Cys35Ser)
c.157T>A (p.Cys53Ser)
gnomAD v4
13g.23203797T>CCA387502559SGCGc.103T>C (p.Cys35Arg)
c.157T>C (p.Cys53Arg)
13g.23203797T>GCA387502560SGCGc.103T>G (p.Cys35Gly)
c.157T>G (p.Cys53Gly)
13g.23203798G>ACA6909573SGCGc.104G>A (p.Cys35Tyr)
c.158G>A (p.Cys53Tyr)
dbSNP ExAC gnomAD v2
13g.23203798G>CCA387502563SGCGc.104G>C (p.Cys35Ser)
c.158G>C (p.Cys53Ser)
gnomAD v4
13g.23203798G=CA2078579944SGCGc.104G= (p.Cys35=)
c.158G= (p.Cys53=)
13g.23203798G>TCA6909572SGCGc.104G>T (p.Cys35Phe)
c.158G>T (p.Cys53Phe)
dbSNP ExAC gnomAD v2 gnomAD v4
13g.23203799T>ACA6909574SGCGc.105T>A (p.Cys35Ter)
c.159T>A (p.Cys53Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.23203799T>CCA482903178SGCGc.105T>C (p.Cys35=)
c.159T>C (p.Cys53=)
gnomAD v4
13g.23203799T>GCA387502566SGCGc.105T>G (p.Cys35Trp)
c.159T>G (p.Cys53Trp)
13g.23203799T=CA2078579945SGCGc.105T= (p.Cys35=)
c.159T= (p.Cys53=)
13g.23203800C>ACA387502567SGCGc.106C>A (p.Leu36Ile)
c.160C>A (p.Leu54Ile)
13g.23203800C>GCA387502568SGCGc.106C>G (p.Leu36Val)
c.160C>G (p.Leu54Val)
13g.23203800C>TCA387502569SGCGc.106C>T (p.Leu36Phe)
c.160C>T (p.Leu54Phe)
13g.23203801T>ACA387502574SGCGc.107T>A (p.Leu36His)
c.161T>A (p.Leu54His)
13g.23203801T>CCA387502570SGCGc.107T>C (p.Leu36Pro)
c.161T>C (p.Leu54Pro)
13g.23203801T>GCA387502572SGCGc.107T>G (p.Leu36Arg)
c.161T>G (p.Leu54Arg)
gnomAD v4
13g.23203802C>ACA482903179SGCGc.108C>A (p.Leu36=)
c.162C>A (p.Leu54=)
13g.23203802C>GCA482903180SGCGc.108C>G (p.Leu36=)
c.162C>G (p.Leu54=)
COSMIC
13g.23203802C>TCA482903181SGCGc.108C>T (p.Leu36=)
c.162C>T (p.Leu54=)
13g.23203803T>ACA387502577SGCGc.109T>A (p.Tyr37Asn)
c.163T>A (p.Tyr55Asn)
13g.23203803T>CCA387502578SGCGc.109T>C (p.Tyr37His)
c.163T>C (p.Tyr55His)
13g.23203803T>GCA387502580SGCGc.109T>G (p.Tyr37Asp)
c.163T>G (p.Tyr55Asp)

Number of alleles fetched