Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.116765215C>T | CA451904726 | FAM162B | c.213G>A (p.Gln71=) | dbSNP |
6 | g.116765215C>A | CA3972193 | FAM162B | c.213G>T (p.Gln71His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.116765215C>G | CA365416899 | FAM162B | c.213G>C (p.Gln71His) | dbSNP |