Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.112957712C>A | CA214100419 | TCF7L2 | c.381+6105C>A (n.381+6105C>A) c.222+6105C>A (n.222+6105C>A) c.63+6105C>A (n.63+6105C>A) | dbSNP |
10 | g.112957712C>G | CA13229381 | TCF7L2 | c.381+6105C>G (n.381+6105C>G) c.222+6105C>G (n.222+6105C>G) c.63+6105C>G (n.63+6105C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.112957712C>T | CA214100420 | TCF7L2 | c.381+6105C>T (n.381+6105C>T) c.222+6105C>T (n.222+6105C>T) c.63+6105C>T (n.63+6105C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |