Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.81115402G>C | CA1558686194 | RASGRF2 | c.2470+1482G>C (n.2470+1482G>C) c.2185+1482G>C (n.2185+1482G>C) n.2537+1482G>C | dbSNP |
5 | g.81115402G>A | CA12030075 | RASGRF2 | c.2470+1482G>A (n.2470+1482G>A) c.2185+1482G>A (n.2185+1482G>A) n.2537+1482G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |