| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.40426601C>T | CA12585996 | SUGCT | c.817-22686C>T (n.817-22686C>T) c.673-22686C>T (n.673-22686C>T) c.838-22686C>T (n.838-22686C>T) c.694-22686C>T (n.694-22686C>T) c.822-22686C>T c.727-22686C>T (n.727-22686C>T) c.760-22686C>T (n.760-22686C>T) c.715-22686C>T (n.715-22686C>T) c.706-22686C>T (n.706-22686C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.40426601C= | CA1701937248 | SUGCT | c.817-22686C= (n.817-22686C=) c.673-22686C= (n.673-22686C=) c.838-22686C= (n.838-22686C=) c.694-22686C= (n.694-22686C=) c.822-22686C= c.727-22686C= (n.727-22686C=) c.760-22686C= (n.760-22686C=) c.715-22686C= (n.715-22686C=) c.706-22686C= (n.706-22686C=) | dbSNP |