Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.215397898A>C | CA2094728 | FN1 | c.3349-50T>G (n.3349-50T>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.215397898A>G | CA1327356560 | FN1 | c.3349-50T>C (n.3349-50T>C) | dbSNP gnomAD v4 |
2 | g.215397898A>T | CA1327356558 | FN1 | c.3349-50T>A (n.3349-50T>A) | dbSNP gnomAD v4 |