| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.53066198G>C | CA1365150288 | c.317+11490C>G c.464+11490C>G c.447+11490C>G | dbSNP | |
| 3 | g.53066198G>T | CA15259731 | c.317+11490C>A c.464+11490C>A c.447+11490C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
| 3 | g.53066198G= | CA1365150287 | c.317+11490C= c.464+11490C= c.447+11490C= | dbSNP |