| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 20 | g.46659814G>T | CA744886483 | SLC13A3 | c.-31+10229C>A (n.-31+10229C>A) c.-31+24582C>A (n.-31+24582C>A) | dbSNP |
| 20 | g.46659814G>A | CA315740778 | SLC13A3 | c.-31+10229C>T (n.-31+10229C>T) c.-31+24582C>T (n.-31+24582C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |