Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.47349923C>A | CA015338 | MYBPC3 | c.506-1G>T (n.506-1G>T) | ClinVar dbSNP gnomAD v4 |
11 | g.47349923C>T | CA380338276 | MYBPC3 | c.506-1G>A (n.506-1G>A) | ClinVar dbSNP |
11 | g.47349923C>G | CA015332 | MYBPC3 | c.506-1G>C (n.506-1G>C) | dbSNP |
11 | g.47349923C= | CA1969341805 | MYBPC3 | c.506-1G= (n.506-1G=) | dbSNP |