Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.18599620G>ACA9314277CRLF1c.342C>T (p.Leu114=)
c.276C>T (p.Leu92=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.18599620G>CCA306262248CRLF1c.342C>G (p.Leu114=)
c.276C>G (p.Leu92=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.18599620G=CA2326433796CRLF1c.342C= (p.Leu114=)
c.276C= (p.Leu92=)
19g.18599620G>TCA506044588CRLF1c.342C>A (p.Leu114=)
c.276C>A (p.Leu92=)
19g.18599621A=CA2326433797CRLF1c.341T= (p.Leu114=)
c.275T= (p.Leu92=)
19g.18599621A>CCA404851908CRLF1c.341T>G (p.Leu114Arg)
c.275T>G (p.Leu92Arg)
19g.18599621A>GCA9314278CRLF1c.341T>C (p.Leu114Pro)
c.275T>C (p.Leu92Pro)
dbSNP ExAC gnomAD v2
19g.18599621A>TCA404851909CRLF1c.341T>A (p.Leu114His)
c.275T>A (p.Leu92His)
19g.18599621_18599624delinsGGGACA2695228420CRLF1c.338_341delinsTCCC (p.Asn113_Leu114delinsIlePro)
c.272_275delinsTCCC (p.Asn91_Leu92delinsIlePro)
19g.18599622G>ACA404851910CRLF1c.340C>T (p.Leu114Phe)
c.274C>T (p.Leu92Phe)
gnomAD v4
19g.18599622G>CCA404851911CRLF1c.340C>G (p.Leu114Val)
c.274C>G (p.Leu92Val)
19g.18599622G>TCA404851912CRLF1c.340C>A (p.Leu114Ile)
c.274C>A (p.Leu92Ile)
19g.18599623G>ACA506044589CRLF1c.339C>T (p.Asn113=)
c.273C>T (p.Asn91=)
19g.18599623G>CCA404851913CRLF1c.339C>G (p.Asn113Lys)
c.273C>G (p.Asn91Lys)
19g.18599623G=CA2326433798CRLF1c.339C= (p.Asn113=)
c.273C= (p.Asn91=)
19g.18599623G>TCA9314279CRLF1c.339C>A (p.Asn113Lys)
c.273C>A (p.Asn91Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.18599624T>ACA404851914CRLF1c.338A>T (p.Asn113Ile)
c.272A>T (p.Asn91Ile)
19g.18599624T>CCA404851916CRLF1c.338A>G (p.Asn113Ser)
c.272A>G (p.Asn91Ser)
19g.18599624T>GCA404851915CRLF1c.338A>C (p.Asn113Thr)
c.272A>C (p.Asn91Thr)
19g.18599625T>ACA404851917CRLF1c.337A>T (p.Asn113Tyr)
c.271A>T (p.Asn91Tyr)
dbSNP gnomAD v2 gnomAD v4
19g.18599625T>CCA404851918CRLF1c.337A>G (p.Asn113Asp)
c.271A>G (p.Asn91Asp)
19g.18599625T>GCA404851919CRLF1c.337A>C (p.Asn113His)
c.271A>C (p.Asn91His)
19g.18599625T=CA2326433799CRLF1c.337A= (p.Asn113=)
c.271A= (p.Asn91=)
19g.18599626G>ACA506044590CRLF1c.336C>T (p.Asp112=)
c.270C>T (p.Asp90=)
19g.18599626G>CCA404851920CRLF1c.336C>G (p.Asp112Glu)
c.270C>G (p.Asp90Glu)
19g.18599626G>TCA404851921CRLF1c.336C>A (p.Asp112Glu)
c.270C>A (p.Asp90Glu)
COSMIC
19g.18599627T>ACA404851922CRLF1c.335A>T (p.Asp112Val)
c.269A>T (p.Asp90Val)
COSMIC
19g.18599627T>CCA404851923CRLF1c.335A>G (p.Asp112Gly)
c.269A>G (p.Asp90Gly)
19g.18599627T>GCA404851924CRLF1c.335A>C (p.Asp112Ala)
c.269A>C (p.Asp90Ala)
19g.18599628C>ACA404851925CRLF1c.334G>T (p.Asp112Tyr)
c.268G>T (p.Asp90Tyr)
gnomAD v4
19g.18599628C>GCA404851926CRLF1c.334G>C (p.Asp112His)
c.268G>C (p.Asp90His)
19g.18599628C>TCA404851927CRLF1c.334G>A (p.Asp112Asn)
c.268G>A (p.Asp90Asn)
gnomAD v4 COSMIC
19g.18599632dupCA2583603679CRLF1c.334dup (p.Asp112GlyfsTer9)
c.268dup (p.Asp90GlyfsTer9)
gnomAD v4
19g.18599629C>ACA506044591CRLF1c.333G>T (p.Gly111=)
c.267G>T (p.Gly89=)
19g.18599629C>GCA506044593CRLF1c.333G>C (p.Gly111=)
c.267G>C (p.Gly89=)
19g.18599629C>TCA506044592CRLF1c.333G>A (p.Gly111=)
c.267G>A (p.Gly89=)
19g.18599630C>ACA404851930CRLF1c.332G>T (p.Gly111Val)
c.266G>T (p.Gly89Val)
gnomAD v4
19g.18599630C=CA2326433800CRLF1c.332G= (p.Gly111=)
c.266G= (p.Gly89=)
19g.18599630C>GCA404851929CRLF1c.332G>C (p.Gly111Ala)
c.266G>C (p.Gly89Ala)
19g.18599630C>TCA404851928CRLF1c.332G>A (p.Gly111Glu)
c.266G>A (p.Gly89Glu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.18599631C>ACA404851931CRLF1c.331G>T (p.Gly111Trp)
c.265G>T (p.Gly89Trp)
19g.18599631C>GCA404851932CRLF1c.331G>C (p.Gly111Arg)
c.265G>C (p.Gly89Arg)
19g.18599631C>TCA404851933CRLF1c.331G>A (p.Gly111Arg)
c.265G>A (p.Gly89Arg)
19g.18599632C>ACA506044594CRLF1c.330G>T (p.Ser110=)
c.264G>T (p.Ser88=)
dbSNP gnomAD v2
19g.18599632C=CA2326433801CRLF1c.330G= (p.Ser110=)
c.264G= (p.Ser88=)
19g.18599632C>GCA506044595CRLF1c.330G>C (p.Ser110=)
c.264G>C (p.Ser88=)
19g.18599632C>TCA506044596CRLF1c.330G>A (p.Ser110=)
c.264G>A (p.Ser88=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.18599633G>ACA404851934CRLF1c.329C>T (p.Ser110Leu)
c.263C>T (p.Ser88Leu)
dbSNP gnomAD v4
19g.18599633G>CCA404851935CRLF1c.329C>G (p.Ser110Trp)
c.263C>G (p.Ser88Trp)
19g.18599633G=CA2326433802CRLF1c.329C= (p.Ser110=)
c.263C= (p.Ser88=)

Number of alleles fetched