Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.14000092T>G | CA1953569759 | SPON1 | c.345+17139T>G (n.345+17139T>G) | dbSNP |
11 | g.14000092T>C | CA13478546 | SPON1 | c.345+17139T>C (n.345+17139T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.14000092T>A | CA1953569760 | SPON1 | c.345+17139T>A (n.345+17139T>A) | dbSNP |