Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.49429505G>T | CA15943070 | SLC17A7 | c.*1014C>A (n.*1014C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.49429505G>C | CA2340398353 | SLC17A7 | c.*1014C>G (n.*1014C>G) | dbSNP gnomAD v4 |
19 | g.49429505G>A | CA883097285 | SLC17A7 | c.*1014C>T (n.*1014C>T) | dbSNP |