Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.23201811C>G | CA4674852 | TNFRSF10A | c.626G>C (p.Arg209Thr) c.20G>C (p.Arg7Thr) c.152G>C (p.Arg51Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.23201811C>A | CA370577729 | TNFRSF10A | c.626G>T (p.Arg209Ile) c.20G>T (p.Arg7Ile) c.152G>T (p.Arg51Ile) | dbSNP |
8 | g.23201811C= | CA1630835131 | TNFRSF10A | c.626G= (p.Arg209=) c.20G= (p.Arg7=) c.152G= (p.Arg51=) | dbSNP |
8 | g.23201811C>T | CA370577730 | TNFRSF10A | c.626G>A (p.Arg209Lys) c.20G>A (p.Arg7Lys) c.152G>A (p.Arg51Lys) | dbSNP gnomAD v4 |