Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.48703374A=CA2340029997FUT2c.418A= (p.Ile140=)
n.475T=
19g.48703374A>CCA406710268FUT2c.418A>C (p.Ile140Leu)
n.475T>G
dbSNP
19g.48703374A>GCA406710271FUT2c.418A>G (p.Ile140Val)
n.475T>C
19g.48703374A>TCA122800FUT2c.418A>T (p.Ile140Phe)
n.475T>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48703375T>ACA406710274FUT2c.419T>A (p.Ile140Asn)
n.474A>T
dbSNP
19g.48703375T>CCA406710276FUT2c.419T>C (p.Ile140Thr)
n.474A>G
19g.48703375T>GCA406710277FUT2c.419T>G (p.Ile140Ser)
n.474A>C
19g.48703375T=CA2340029998FUT2c.419T= (p.Ile140=)
n.474A=
19g.48703376C>ACA508272354FUT2c.420C>A (p.Ile140=)
n.473G>T
19g.48703376C=CA2340029999FUT2c.420C= (p.Ile140=)
n.473G=
19g.48703376C>GCA406710280FUT2c.420C>G (p.Ile140Met)
n.473G>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48703376C>TCA508272353FUT2c.420C>T (p.Ile140=)
n.473G>A
dbSNP gnomAD v3 gnomAD v4
19g.48703377C>ACA406710283FUT2c.421C>A (p.Pro141Thr)
n.472G>T
gnomAD v4
19g.48703377C>GCA406710285FUT2c.421C>G (p.Pro141Ala)
n.472G>C
19g.48703377C>TCA406710287FUT2c.421C>T (p.Pro141Ser)
n.472G>A
19g.48703378C>ACA406710290FUT2c.422C>A (p.Pro141Gln)
n.471G>T
gnomAD v4
19g.48703378C=CA2340030000FUT2c.422C= (p.Pro141=)
n.471G=
19g.48703378C>GCA9556238FUT2c.422C>G (p.Pro141Arg)
n.471G>C
dbSNP ExAC gnomAD v2 gnomAD v4
19g.48703378C>TCA9556239FUT2c.422C>T (p.Pro141Leu)
n.471G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48703379G>ACA9556241FUT2c.423G>A (p.Pro141=)
n.470C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.48703379G>CCA9556242FUT2c.423G>C (p.Pro141=)
n.470C>G
dbSNP ExAC gnomAD v2 gnomAD v4
19g.48703379G=CA2340030001FUT2c.423G= (p.Pro141=)
n.470C=
19g.48703379G>TCA9556240FUT2c.423G>T (p.Pro141=)
n.470C>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48703383dupCA2340030002FUT2c.427dup (p.Glu143GlyfsTer?)
n.470dup
dbSNP
19g.48703383delCA645614263FUT2c.427del (p.Glu143SerfsTer?)
n.470del
COSMIC
19g.48703380G>ACA406710302FUT2c.424G>A (p.Gly142Arg)
n.469C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48703380G>CCA406710304FUT2c.424G>C (p.Gly142Arg)
n.469C>G
gnomAD v4
19g.48703380G=CA2340030003FUT2c.424G= (p.Gly142=)
n.469C=
19g.48703380G>TCA406710306FUT2c.424G>T (p.Gly142Trp)
n.469C>A
19g.48703381G>ACA406710307FUT2c.425G>A (p.Gly142Glu)
n.468C>T
COSMIC
19g.48703381G>CCA406710309FUT2c.425G>C (p.Gly142Ala)
n.468C>G
dbSNP gnomAD v2
19g.48703381G=CA2340030004FUT2c.425G= (p.Gly142=)
n.468C=
19g.48703381G>TCA406710310FUT2c.425G>T (p.Gly142Val)
n.468C>A
19g.48703382G>ACA508272367FUT2c.426G>A (p.Gly142=)
n.467C>T
gnomAD v4
19g.48703382G>CCA508272368FUT2c.426G>C (p.Gly142=)
n.467C>G
19g.48703382G>TCA508272369FUT2c.426G>T (p.Gly142=)
n.467C>A
19g.48703382_48703383insCCA2586240159FUT2c.426_427insC (p.Glu143ArgfsTer?)
n.466_467insG
gnomAD v4
19g.48703382_48703383insCGCTCA2586240157FUT2c.426_427insCGCT (p.Glu143ArgfsTer2)
n.466_467insAGCG
gnomAD v4
19g.48703382_48703383insCGCTGTCA2586240158FUT2c.426_427insCGCTGT (p.Gly142_Glu143insArgCys)
n.466_467insACAGCG
gnomAD v4
19g.48703383G>ACA406710311FUT2c.427G>A (p.Glu143Lys)
n.466C>T
19g.48703383G>CCA406710313FUT2c.427G>C (p.Glu143Gln)
n.466C>G
gnomAD v4
19g.48703383G=CA2340030005FUT2c.427G= (p.Glu143=)
n.466C=
19g.48703383G>TCA406710314FUT2c.427G>T (p.Glu143Ter)
n.466C>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48703383_48703384insCCA2340030006FUT2c.427_428insC (p.Glu143AlafsTer?)
n.465_466insG
dbSNP gnomAD v4
19g.48703384A=CA2340030007FUT2c.428A= (p.Glu143=)
n.465T=
19g.48703384A>CCA406710316FUT2c.428A>C (p.Glu143Ala)
n.465T>G
19g.48703384A>GCA406710318FUT2c.428A>G (p.Glu143Gly)
n.465T>C
19g.48703384A>TCA406710320FUT2c.428A>T (p.Glu143Val)
n.465T>A
dbSNP gnomAD v4
19g.48703385G>ACA9556243FUT2c.429G>A (p.Glu143=)
n.464C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48703385G>CCA406710324FUT2c.429G>C (p.Glu143Asp)
n.464C>G

Number of alleles fetched