Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.18599573T>ACA404851808CRLF1c.389A>T (p.Tyr130Phe)
c.323A>T (p.Tyr108Phe)
19g.18599573T>CCA404851810CRLF1c.389A>G (p.Tyr130Cys)
c.323A>G (p.Tyr108Cys)
dbSNP gnomAD v3 gnomAD v4
19g.18599573T>GCA404851809CRLF1c.389A>C (p.Tyr130Ser)
c.323A>C (p.Tyr108Ser)
19g.18599573T=CA2326433776CRLF1c.389A= (p.Tyr130=)
c.323A= (p.Tyr108=)
19g.18599574A>CCA404851811CRLF1c.388T>G (p.Tyr130Asp)
c.322T>G (p.Tyr108Asp)
19g.18599574A>GCA404851812CRLF1c.388T>C (p.Tyr130His)
c.322T>C (p.Tyr108His)
19g.18599574A>TCA404851813CRLF1c.388T>A (p.Tyr130Asn)
c.322T>A (p.Tyr108Asn)
19g.18599575G>ACA506044552CRLF1c.387C>T (p.Leu129=)
c.321C>T (p.Leu107=)
19g.18599575G>CCA506044553CRLF1c.387C>G (p.Leu129=)
c.321C>G (p.Leu107=)
dbSNP gnomAD v3 gnomAD v4
19g.18599575G=CA2326433777CRLF1c.387C= (p.Leu129=)
c.321C= (p.Leu107=)
19g.18599575G>TCA506044554CRLF1c.387C>A (p.Leu129=)
c.321C>A (p.Leu107=)
19g.18599576A>CCA404851814CRLF1c.386T>G (p.Leu129Arg)
c.320T>G (p.Leu107Arg)
19g.18599576A>GCA404851815CRLF1c.386T>C (p.Leu129Pro)
c.320T>C (p.Leu107Pro)
19g.18599576A>TCA404851816CRLF1c.386T>A (p.Leu129His)
c.320T>A (p.Leu107His)
19g.18599578_18599588dupCA2583603678CRLF1c.376_386dup (p.Tyr130AlafsTer23)
c.310_320dup (p.Tyr108AlafsTer23)
gnomAD v4
19g.18599577G>ACA404851817CRLF1c.385C>T (p.Leu129Phe)
c.319C>T (p.Leu107Phe)
19g.18599577G>CCA404851818CRLF1c.385C>G (p.Leu129Val)
c.319C>G (p.Leu107Val)
19g.18599577G>TCA404851819CRLF1c.385C>A (p.Leu129Ile)
c.319C>A (p.Leu107Ile)
19g.18599578delCA2741617212CRLF1c.385del (p.Leu129SerfsTer20)
c.319del (p.Leu107SerfsTer20)
19g.18599578G>ACA506044555CRLF1c.384C>T (p.Cys128=)
c.318C>T (p.Cys106=)
COSMIC
19g.18599578G>CCA404851820CRLF1c.384C>G (p.Cys128Trp)
c.318C>G (p.Cys106Trp)
19g.18599578G>TCA404851821CRLF1c.384C>A (p.Cys128Ter)
c.318C>A (p.Cys106Ter)
19g.18599579C>ACA404851823CRLF1c.383G>T (p.Cys128Phe)
c.317G>T (p.Cys106Phe)
19g.18599579C=CA2326433778CRLF1c.383G= (p.Cys128=)
c.317G= (p.Cys106=)
19g.18599579C>GCA404851824CRLF1c.383G>C (p.Cys128Ser)
c.317G>C (p.Cys106Ser)
19g.18599579C>TCA404851822CRLF1c.383G>A (p.Cys128Tyr)
c.317G>A (p.Cys106Tyr)
dbSNP gnomAD v2 gnomAD v4
19g.18599580A=CA2326433779CRLF1c.382T= (p.Cys128=)
c.316T= (p.Cys106=)
19g.18599580A>CCA404851825CRLF1c.382T>G (p.Cys128Gly)
c.316T>G (p.Cys106Gly)
gnomAD v4
19g.18599580A>GCA9314269CRLF1c.382T>C (p.Cys128Arg)
c.316T>C (p.Cys106Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.18599580A>TCA404851826CRLF1c.382T>A (p.Cys128Ser)
c.316T>A (p.Cys106Ser)
19g.18599581G>ACA506044556CRLF1c.381C>T (p.Ser127=)
c.315C>T (p.Ser105=)
19g.18599581G>CCA506044557CRLF1c.381C>G (p.Ser127=)
c.315C>G (p.Ser105=)
19g.18599581G>TCA506044558CRLF1c.381C>A (p.Ser127=)
c.315C>A (p.Ser105=)
19g.18599582G>ACA404851827CRLF1c.380C>T (p.Ser127Phe)
c.314C>T (p.Ser105Phe)
gnomAD v4 COSMIC
19g.18599582G>CCA404851829CRLF1c.380C>G (p.Ser127Cys)
c.314C>G (p.Ser105Cys)
dbSNP gnomAD v2 gnomAD v4
19g.18599582G=CA2326433780CRLF1c.380C= (p.Ser127=)
c.314C= (p.Ser105=)
19g.18599582G>TCA404851828CRLF1c.380C>A (p.Ser127Tyr)
c.314C>A (p.Ser105Tyr)
dbSNP
19g.18599583A>CCA404851830CRLF1c.379T>G (p.Ser127Ala)
c.313T>G (p.Ser105Ala)
19g.18599583A>GCA404851831CRLF1c.379T>C (p.Ser127Pro)
c.313T>C (p.Ser105Pro)
19g.18599583A>TCA404851832CRLF1c.379T>A (p.Ser127Thr)
c.313T>A (p.Ser105Thr)
19g.18599584G>ACA506044559CRLF1c.378C>T (p.Gly126=)
c.312C>T (p.Gly104=)
19g.18599584G>CCA506044560CRLF1c.378C>G (p.Gly126=)
c.312C>G (p.Gly104=)
19g.18599584G>TCA506044561CRLF1c.378C>A (p.Gly126=)
c.312C>A (p.Gly104=)
19g.18599585C>ACA404851833CRLF1c.377G>T (p.Gly126Val)
c.311G>T (p.Gly104Val)
19g.18599585C=CA2326433781CRLF1c.377G= (p.Gly126=)
c.311G= (p.Gly104=)
19g.18599585C>GCA404851834CRLF1c.377G>C (p.Gly126Ala)
c.311G>C (p.Gly104Ala)
dbSNP
19g.18599585C>TCA9314270CRLF1c.377G>A (p.Gly126Asp)
c.311G>A (p.Gly104Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.18599586C>ACA404851835CRLF1c.376G>T (p.Gly126Cys)
c.310G>T (p.Gly104Cys)
19g.18599586C>GCA404851836CRLF1c.376G>C (p.Gly126Arg)
c.310G>C (p.Gly104Arg)
19g.18599586C>TCA404851837CRLF1c.376G>A (p.Gly126Ser)
c.310G>A (p.Gly104Ser)

Number of alleles fetched