Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.104279427A>TCA378085611GSTO2c.424A>T (p.Asn142Tyr)
c.340A>T (p.Asn114Tyr)
c.366+1311A>T (n.366+1311A>T)
n.275+1311A>T
n.311A>T
c.282+1311A>T (n.282+1311A>T)
dbSNP
10g.104279427A>GCA5681860GSTO2c.424A>G (p.Asn142Asp)
c.340A>G (p.Asn114Asp)
c.366+1311A>G (n.366+1311A>G)
n.275+1311A>G
n.311A>G
c.282+1311A>G (n.282+1311A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.104279427A>CCA378085609GSTO2c.424A>C (p.Asn142His)
c.340A>C (p.Asn114His)
c.366+1311A>C (n.366+1311A>C)
n.275+1311A>C
n.311A>C
c.282+1311A>C (n.282+1311A>C)
dbSNP
10g.104279427A=CA1933517614GSTO2c.424A= (p.Asn142=)
c.340A= (p.Asn114=)
c.366+1311A= (n.366+1311A=)
n.275+1311A=
n.311A=
c.282+1311A= (n.282+1311A=)
dbSNP

Number of alleles fetched