| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.71655902C>G | CA1174933368 | NEGR1 | c.667+42106G>C (n.667+42106G>C) c.283+42106G>C (n.283+42106G>C) c.502+42106G>C (n.502+42106G>C) | dbSNP |
| 1 | g.71655902C>A | CA10729183 | NEGR1 | c.667+42106G>T (n.667+42106G>T) c.283+42106G>T (n.283+42106G>T) c.502+42106G>T (n.502+42106G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.71655902C= | CA1139843024 | NEGR1 | c.667+42106G= (n.667+42106G=) c.283+42106G= (n.283+42106G=) c.502+42106G= (n.502+42106G=) | dbSNP |