Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.135637876G>T | CA1883798881 | GLT6D1 | c.71+1241C>A (n.71+1241C>A) | dbSNP |
9 | g.135637876G>A | CA1883798882 | GLT6D1 | c.71+1241C>T (n.71+1241C>T) | dbSNP |
9 | g.135637876G>C | CA201440931 | GLT6D1 | c.71+1241C>G (n.71+1241C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |