Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.89769208C>G | CA940682335 | TRIM49 | c.739-372G>C (n.739-372G>C) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.89769208C>A | CA13424945 | TRIM49 | c.739-372G>T (n.739-372G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.89769208C>T | CA1990208793 | TRIM49 | c.739-372G>A (n.739-372G>A) | dbSNP |