Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
Y | g.7700527C>G | CA337593088 | RFTN1P1,TTTY16 | n.753+660G>C n.61+660G>C | dbSNP gnomAD v3 gnomAD v4 |
Y | g.7700527C>A | CA337593087 | RFTN1P1,TTTY16 | n.753+660G>T n.61+660G>T | dbSNP gnomAD v3 gnomAD v4 |
Y | g.7700527C= | CA2469950877 | RFTN1P1,TTTY16 | n.753+660G= n.61+660G= | dbSNP |