Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.48703460C>ACA406710717FUT2c.504C>A (p.Phe168Leu)
n.389G>T
19g.48703460C=CA2340030051FUT2c.504C= (p.Phe168=)
n.389G=
19g.48703460C>GCA406710716FUT2c.504C>G (p.Phe168Leu)
n.389G>C
19g.48703460C>TCA508272594FUT2c.504C>T (p.Phe168=)
n.389G>A
dbSNP gnomAD v4
19g.48703461A=CA2340030052FUT2c.505A= (p.Thr169=)
n.388T=
19g.48703461A>CCA406710721FUT2c.505A>C (p.Thr169Pro)
n.388T>G
dbSNP
19g.48703461A>GCA406710723FUT2c.505A>G (p.Thr169Ala)
n.388T>C
19g.48703461A>TCA406710725FUT2c.505A>T (p.Thr169Ser)
n.388T>A
19g.48703462C>ACA406710727FUT2c.506C>A (p.Thr169Asn)
n.387G>T
19g.48703462C=CA2340030053FUT2c.506C= (p.Thr169=)
n.387G=
19g.48703462C>GCA406710729FUT2c.506C>G (p.Thr169Ser)
n.387G>C
19g.48703462C>TCA406710731FUT2c.506C>T (p.Thr169Ile)
n.387G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48703463C>ACA508272595FUT2c.507C>A (p.Thr169=)
n.386G>T
19g.48703463C>GCA508272596FUT2c.507C>G (p.Thr169=)
n.386G>C
19g.48703463C>TCA508272597FUT2c.507C>T (p.Thr169=)
n.386G>A
19g.48703464C>ACA406710734FUT2c.508C>A (p.Leu170Met)
n.385G>T
19g.48703464C=CA2340030054FUT2c.508C= (p.Leu170=)
n.385G=
19g.48703464C>GCA406710736FUT2c.508C>G (p.Leu170Val)
n.385G>C
19g.48703464C>TCA508272598FUT2c.508C>T (p.Leu170=)
n.385G>A
dbSNP gnomAD v4
19g.48703465T>ACA406710739FUT2c.509T>A (p.Leu170Gln)
n.384A>T
19g.48703465T>CCA406710741FUT2c.509T>C (p.Leu170Pro)
n.384A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48703465T>GCA406710743FUT2c.509T>G (p.Leu170Arg)
n.384A>C
19g.48703465T=CA2340030055FUT2c.509T= (p.Leu170=)
n.384A=
19g.48703466G>ACA508272600FUT2c.510G>A (p.Leu170=)
n.383C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48703466G>CCA508272601FUT2c.510G>C (p.Leu170=)
n.383C>G
19g.48703466G=CA2340030056FUT2c.510G= (p.Leu170=)
n.383C=
19g.48703466G>TCA508272599FUT2c.510G>T (p.Leu170=)
n.383C>A
19g.48703467C>ACA406710748FUT2c.511C>A (p.His171Asn)
n.382G>T
19g.48703467C=CA2340030057FUT2c.511C= (p.His171=)
n.382G=
19g.48703467C>GCA406710751FUT2c.511C>G (p.His171Asp)
n.382G>C
19g.48703467C>TCA406710746FUT2c.511C>T (p.His171Tyr)
n.382G>A
dbSNP gnomAD v2 gnomAD v4
19g.48703468A=CA2340030058FUT2c.512A= (p.His171=)
n.381T=
19g.48703468A>CCA406710754FUT2c.512A>C (p.His171Pro)
n.381T>G
19g.48703468A>GCA406710756FUT2c.512A>G (p.His171Arg)
n.381T>C
dbSNP
19g.48703468A>TCA406710758FUT2c.512A>T (p.His171Leu)
n.381T>A
19g.48703469C>ACA406710761FUT2c.513C>A (p.His171Gln)
n.380G>T
19g.48703469C=CA2340030059FUT2c.513C= (p.His171=)
n.380G=
19g.48703469C>GCA309352445FUT2c.513C>G (p.His171Gln)
n.380G>C
dbSNP gnomAD v3 gnomAD v4
19g.48703469C>TCA9556259FUT2c.513C>T (p.His171=)
n.380G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48703470G>ACA9556260FUT2c.514G>A (p.Asp172Asn)
n.379C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48703470G>CCA406710767FUT2c.514G>C (p.Asp172His)
n.379C>G
19g.48703470G=CA2340030060FUT2c.514G= (p.Asp172=)
n.379C=
19g.48703470G>TCA406710769FUT2c.514G>T (p.Asp172Tyr)
n.379C>A
gnomAD v4
19g.48703471A=CA2340030061FUT2c.515A= (p.Asp172=)
n.378T=
19g.48703471A>CCA406710773FUT2c.515A>C (p.Asp172Ala)
n.378T>G
19g.48703471A>GCA406710776FUT2c.515A>G (p.Asp172Gly)
n.378T>C
dbSNP gnomAD v3 gnomAD v4
19g.48703471A>TCA406710778FUT2c.515A>T (p.Asp172Val)
n.378T>A
19g.48703472C>ACA406710781FUT2c.516C>A (p.Asp172Glu)
n.377G>T
19g.48703472C=CA2340030062FUT2c.516C= (p.Asp172=)
n.377G=
19g.48703472C>GCA406710783FUT2c.516C>G (p.Asp172Glu)
n.377G>C
dbSNP gnomAD v2

Number of alleles fetched