Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.72195289A>CCA381731700FOLR1c.187A>C (p.Asn63His)
11g.72195289A>GCA381731703FOLR1c.187A>G (p.Asn63Asp)
11g.72195289A>TCA381731704FOLR1c.187A>T (p.Asn63Tyr)
11g.72195290A>CCA381731705FOLR1c.188A>C (p.Asn63Thr)
11g.72195290A>GCA381731706FOLR1c.188A>G (p.Asn63Ser)
11g.72195290A>TCA381731709FOLR1c.188A>T (p.Asn63Ile)
11g.72195291T>ACA381731712FOLR1c.189T>A (p.Asn63Lys)
11g.72195291T>CCA475596861FOLR1c.189T>C (p.Asn63=)
11g.72195291T>GCA381731714FOLR1c.189T>G (p.Asn63Lys)
11g.72195292G>ACA381731717FOLR1c.190G>A (p.Ala64Thr)
COSMIC
11g.72195292G>CCA381731726FOLR1c.190G>C (p.Ala64Pro)
11g.72195292G=CA1981879903FOLR1c.190G= (p.Ala64=)
11g.72195292G>TCA381731727FOLR1c.190G>T (p.Ala64Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.72195293C>ACA381731734FOLR1c.191C>A (p.Ala64Asp)
dbSNP gnomAD v4
11g.72195293C=CA1981879904FOLR1c.191C= (p.Ala64=)
11g.72195293C>GCA381731730FOLR1c.191C>G (p.Ala64Gly)
11g.72195293C>TCA381731732FOLR1c.191C>T (p.Ala64Val)
11g.72195294C>ACA475596870FOLR1c.192C>A (p.Ala64=)
11g.72195294C=CA1981879905FOLR1c.192C= (p.Ala64=)
11g.72195294C>GCA475596874FOLR1c.192C>G (p.Ala64=)
11g.72195294C>TCA16606327FOLR1c.192C>T (p.Ala64=)
ClinVar dbSNP
11g.72195295T>ACA381731736FOLR1c.193T>A (p.Cys65Ser)
11g.72195295T>CCA381731737FOLR1c.193T>C (p.Cys65Arg)
11g.72195295T>GCA381731742FOLR1c.193T>G (p.Cys65Gly)
11g.72195296G>ACA381731748FOLR1c.194G>A (p.Cys65Tyr)
dbSNP gnomAD v3 gnomAD v4
11g.72195296G>CCA381731752FOLR1c.194G>C (p.Cys65Ser)
11g.72195296G=CA1981879906FOLR1c.194G= (p.Cys65=)
11g.72195296G>TCA381731753FOLR1c.194G>T (p.Cys65Phe)
11g.72195297C>ACA381731756FOLR1c.195C>A (p.Cys65Ter)
11g.72195297C=CA1981879907FOLR1c.195C= (p.Cys65=)
11g.72195297C>GCA381731759FOLR1c.195C>G (p.Cys65Trp)
dbSNP gnomAD v2 gnomAD v4
11g.72195297C>TCA475596886FOLR1c.195C>T (p.Cys65=)
gnomAD v4
11g.72195298T>ACA381731769FOLR1c.196T>A (p.Cys66Ser)
11g.72195298T>CCA381731772FOLR1c.196T>C (p.Cys66Arg)
11g.72195298T>GCA381731777FOLR1c.196T>G (p.Cys66Gly)
11g.72195299G>ACA6169138FOLR1c.197G>A (p.Cys66Tyr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.72195299G>CCA381731785FOLR1c.197G>C (p.Cys66Ser)
11g.72195299G=CA1981879908FOLR1c.197G= (p.Cys66=)
11g.72195299G>TCA381731782FOLR1c.197G>T (p.Cys66Phe)
11g.72195300T>ACA381731789FOLR1c.198T>A (p.Cys66Ter)
11g.72195300T>CCA475596897FOLR1c.198T>C (p.Cys66=)
ClinVar
11g.72195300T>GCA381731792FOLR1c.198T>G (p.Cys66Trp)
11g.72195301T>ACA381731798FOLR1c.199T>A (p.Ser67Thr)
11g.72195301T>CCA381731801FOLR1c.199T>C (p.Ser67Pro)
11g.72195301T>GCA381731803FOLR1c.199T>G (p.Ser67Ala)
11g.72195302C>ACA381731815FOLR1c.200C>A (p.Ser67Tyr)
COSMIC
11g.72195302C>GCA381731812FOLR1c.200C>G (p.Ser67Cys)
11g.72195302C>TCA381731808FOLR1c.200C>T (p.Ser67Phe)
11g.72195303T>ACA475596909FOLR1c.201T>A (p.Ser67=)
11g.72195303T>CCA475596907FOLR1c.201T>C (p.Ser67=)

Number of alleles fetched