Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.23201811C>GCA4674852TNFRSF10Ac.626G>C (p.Arg209Thr)
c.20G>C (p.Arg7Thr)
c.152G>C (p.Arg51Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.23201811C>ACA370577729TNFRSF10Ac.626G>T (p.Arg209Ile)
c.20G>T (p.Arg7Ile)
c.152G>T (p.Arg51Ile)
dbSNP
8g.23201811C=CA1630835131TNFRSF10Ac.626G= (p.Arg209=)
c.20G= (p.Arg7=)
c.152G= (p.Arg51=)
dbSNP
8g.23201811C>TCA370577730TNFRSF10Ac.626G>A (p.Arg209Lys)
c.20G>A (p.Arg7Lys)
c.152G>A (p.Arg51Lys)
dbSNP gnomAD v4

Number of alleles fetched