Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.76143375A>T | CA1077640061 | SV2C | c.580+11045A>T (n.580+11045A>T) c.8+11045A>T (n.8+11045A>T) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.76143375A>G | CA121234563 | SV2C | c.580+11045A>G (n.580+11045A>G) c.8+11045A>G (n.8+11045A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |