| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| Y | g.12833680C>T | CA2589297628 | USP9Y | c.5022-8C>T (n.5022-8C>T) n.5034-8C>T c.4788-8C>T (n.4788-8C>T) c.5037-8C>T (n.5037-8C>T) | gnomAD v3 gnomAD v4 |
| Y | g.12833683_12833685del | CA1139272056 | USP9Y | c.5022-5_5022-3del (n.5022-5_5022-3del) n.5034-5_5034-3del c.4788-5_4788-3del (n.4788-5_4788-3del) c.5037-5_5037-3del (n.5037-5_5037-3del) | gnomAD v3 gnomAD v4 |
| Y | g.12833686A>C | CA414998583 | USP9Y | c.5022-2A>C (n.5022-2A>C) n.5034-2A>C c.4788-2A>C (n.4788-2A>C) c.5037-2A>C (n.5037-2A>C) | |
| Y | g.12833686A>G | CA414998585 | USP9Y | c.5022-2A>G (n.5022-2A>G) n.5034-2A>G c.4788-2A>G (n.4788-2A>G) c.5037-2A>G (n.5037-2A>G) | |
| Y | g.12833686A>T | CA414998587 | USP9Y | c.5022-2A>T (n.5022-2A>T) n.5034-2A>T c.4788-2A>T (n.4788-2A>T) c.5037-2A>T (n.5037-2A>T) | |
| Y | g.12833687G>A | CA414998589 | USP9Y | c.5022-1G>A (n.5022-1G>A) n.5034-1G>A c.4788-1G>A (n.4788-1G>A) c.5037-1G>A (n.5037-1G>A) | |
| Y | g.12833687G>C | CA414998591 | USP9Y | c.5022-1G>C (n.5022-1G>C) n.5034-1G>C c.4788-1G>C (n.4788-1G>C) c.5037-1G>C (n.5037-1G>C) | |
| Y | g.12833687G>T | CA414998592 | USP9Y | c.5022-1G>T (n.5022-1G>T) n.5034-1G>T c.4788-1G>T (n.4788-1G>T) c.5037-1G>T (n.5037-1G>T) | |
| Y | g.12833688G>A | CA519901419 | USP9Y | c.5022G>A (p.Arg1674=) n.5034G>A c.4788G>A (p.Arg1596=) c.5037G>A (p.Arg1679=) | |
| Y | g.12833688G>C | CA414998595 | USP9Y | c.5022G>C (p.Arg1674Ser) n.5034G>C c.4788G>C (p.Arg1596Ser) c.5037G>C (p.Arg1679Ser) | |
| Y | g.12833688G>T | CA414998596 | USP9Y | c.5022G>T (p.Arg1674Ser) n.5034G>T c.4788G>T (p.Arg1596Ser) c.5037G>T (p.Arg1679Ser) | |
| Y | g.12833689C>A | CA414998599 | USP9Y | c.5023C>A (p.Leu1675Ile) n.5035C>A c.4789C>A (p.Leu1597Ile) c.5038C>A (p.Leu1680Ile) | |
| Y | g.12833689C>G | CA414998601 | USP9Y | c.5023C>G (p.Leu1675Val) n.5035C>G c.4789C>G (p.Leu1597Val) c.5038C>G (p.Leu1680Val) | |
| Y | g.12833689C>T | CA414998602 | USP9Y | c.5023C>T (p.Leu1675Phe) n.5035C>T c.4789C>T (p.Leu1597Phe) c.5038C>T (p.Leu1680Phe) | |
| Y | g.12833690T>A | CA414998608 | USP9Y | c.5024T>A (p.Leu1675His) n.5036T>A c.4790T>A (p.Leu1597His) c.5039T>A (p.Leu1680His) | |
| Y | g.12833690T>C | CA414998607 | USP9Y | c.5024T>C (p.Leu1675Pro) n.5036T>C c.4790T>C (p.Leu1597Pro) c.5039T>C (p.Leu1680Pro) | |
| Y | g.12833690T>G | CA414998605 | USP9Y | c.5024T>G (p.Leu1675Arg) n.5036T>G c.4790T>G (p.Leu1597Arg) c.5039T>G (p.Leu1680Arg) | |
| Y | g.12833691T>A | CA519901429 | USP9Y | c.5025T>A (p.Leu1675=) n.5037T>A c.4791T>A (p.Leu1597=) c.5040T>A (p.Leu1680=) | |
| Y | g.12833691T>C | CA519901431 | USP9Y | c.5025T>C (p.Leu1675=) n.5037T>C c.4791T>C (p.Leu1597=) c.5040T>C (p.Leu1680=) | |
| Y | g.12833691T>G | CA519901432 | USP9Y | c.5025T>G (p.Leu1675=) n.5037T>G c.4791T>G (p.Leu1597=) c.5040T>G (p.Leu1680=) | |
| Y | g.12833692T>A | CA414998611 | USP9Y | c.5026T>A (p.Trp1676Arg) n.5038T>A c.4792T>A (p.Trp1598Arg) c.5041T>A (p.Trp1681Arg) | |
| Y | g.12833692T>C | CA414998612 | USP9Y | c.5026T>C (p.Trp1676Arg) n.5038T>C c.4792T>C (p.Trp1598Arg) c.5041T>C (p.Trp1681Arg) | |
| Y | g.12833692T>G | CA414998614 | USP9Y | c.5026T>G (p.Trp1676Gly) n.5038T>G c.4792T>G (p.Trp1598Gly) c.5041T>G (p.Trp1681Gly) | |
| Y | g.12833693G>A | CA414998617 | USP9Y | c.5027G>A (p.Trp1676Ter) n.5039G>A c.4793G>A (p.Trp1598Ter) c.5042G>A (p.Trp1681Ter) | |
| Y | g.12833693G>C | CA414998618 | USP9Y | c.5027G>C (p.Trp1676Ser) n.5039G>C c.4793G>C (p.Trp1598Ser) c.5042G>C (p.Trp1681Ser) | |
| Y | g.12833693G>T | CA414998619 | USP9Y | c.5027G>T (p.Trp1676Leu) n.5039G>T c.4793G>T (p.Trp1598Leu) c.5042G>T (p.Trp1681Leu) | |
| Y | g.12833694G>A | CA414998621 | USP9Y | c.5028G>A (p.Trp1676Ter) n.5040G>A c.4794G>A (p.Trp1598Ter) c.5043G>A (p.Trp1681Ter) | |
| Y | g.12833694G>C | CA414998623 | USP9Y | c.5028G>C (p.Trp1676Cys) n.5040G>C c.4794G>C (p.Trp1598Cys) c.5043G>C (p.Trp1681Cys) | |
| Y | g.12833694G>T | CA414998625 | USP9Y | c.5028G>T (p.Trp1676Cys) n.5040G>T c.4794G>T (p.Trp1598Cys) c.5043G>T (p.Trp1681Cys) | |
| Y | g.12833695G>A | CA414998627 | USP9Y | c.5029G>A (p.Gly1677Ser) n.5041G>A c.4795G>A (p.Gly1599Ser) c.5044G>A (p.Gly1682Ser) | |
| Y | g.12833695G>C | CA414998628 | USP9Y | c.5029G>C (p.Gly1677Arg) n.5041G>C c.4795G>C (p.Gly1599Arg) c.5044G>C (p.Gly1682Arg) | |
| Y | g.12833695G>T | CA414998630 | USP9Y | c.5029G>T (p.Gly1677Cys) n.5041G>T c.4795G>T (p.Gly1599Cys) c.5044G>T (p.Gly1682Cys) | |
| Y | g.12833696G>A | CA414998634 | USP9Y | c.5030G>A (p.Gly1677Asp) n.5042G>A c.4796G>A (p.Gly1599Asp) c.5045G>A (p.Gly1682Asp) | |
| Y | g.12833696G>C | CA414998636 | USP9Y | c.5030G>C (p.Gly1677Ala) n.5042G>C c.4796G>C (p.Gly1599Ala) c.5045G>C (p.Gly1682Ala) | |
| Y | g.12833696G>T | CA414998632 | USP9Y | c.5030G>T (p.Gly1677Val) n.5042G>T c.4796G>T (p.Gly1599Val) c.5045G>T (p.Gly1682Val) | |
| Y | g.12833697T>A | CA519901450 | USP9Y | c.5031T>A (p.Gly1677=) n.5043T>A c.4797T>A (p.Gly1599=) c.5046T>A (p.Gly1682=) | |
| Y | g.12833697T>C | CA519901452 | USP9Y | c.5031T>C (p.Gly1677=) n.5043T>C c.4797T>C (p.Gly1599=) c.5046T>C (p.Gly1682=) | |
| Y | g.12833697T>G | CA519901453 | USP9Y | c.5031T>G (p.Gly1677=) n.5043T>G c.4797T>G (p.Gly1599=) c.5046T>G (p.Gly1682=) | |
| Y | g.12833698G>A | CA414998638 | USP9Y | c.5032G>A (p.Glu1678Lys) n.5044G>A c.4798G>A (p.Glu1600Lys) c.5047G>A (p.Glu1683Lys) | |
| Y | g.12833698G>C | CA414998640 | USP9Y | c.5032G>C (p.Glu1678Gln) n.5044G>C c.4798G>C (p.Glu1600Gln) c.5047G>C (p.Glu1683Gln) | |
| Y | g.12833698G>T | CA414998642 | USP9Y | c.5032G>T (p.Glu1678Ter) n.5044G>T c.4798G>T (p.Glu1600Ter) c.5047G>T (p.Glu1683Ter) | |
| Y | g.12833699A>C | CA414998645 | USP9Y | c.5033A>C (p.Glu1678Ala) n.5045A>C c.4799A>C (p.Glu1600Ala) c.5048A>C (p.Glu1683Ala) | |
| Y | g.12833699A>G | CA414998646 | USP9Y | c.5033A>G (p.Glu1678Gly) n.5045A>G c.4799A>G (p.Glu1600Gly) c.5048A>G (p.Glu1683Gly) | |
| Y | g.12833699A>T | CA414998648 | USP9Y | c.5033A>T (p.Glu1678Val) n.5045A>T c.4799A>T (p.Glu1600Val) c.5048A>T (p.Glu1683Val) | |
| Y | g.12833700A>C | CA414998651 | USP9Y | c.5034A>C (p.Glu1678Asp) n.5046A>C c.4800A>C (p.Glu1600Asp) c.5049A>C (p.Glu1683Asp) | |
| Y | g.12833700A>G | CA519901463 | USP9Y | c.5034A>G (p.Glu1678=) n.5046A>G c.4800A>G (p.Glu1600=) c.5049A>G (p.Glu1683=) | |
| Y | g.12833700A>T | CA414998650 | USP9Y | c.5034A>T (p.Glu1678Asp) n.5046A>T c.4800A>T (p.Glu1600Asp) c.5049A>T (p.Glu1683Asp) | |
| Y | g.12833701C>A | CA414998653 | USP9Y | c.5035C>A (p.Pro1679Thr) n.5047C>A c.4801C>A (p.Pro1601Thr) c.5050C>A (p.Pro1684Thr) | |
| Y | g.12833701C>G | CA414998655 | USP9Y | c.5035C>G (p.Pro1679Ala) n.5047C>G c.4801C>G (p.Pro1601Ala) c.5050C>G (p.Pro1684Ala) | |
| Y | g.12833701C>T | CA414998657 | USP9Y | c.5035C>T (p.Pro1679Ser) n.5047C>T c.4801C>T (p.Pro1601Ser) c.5050C>T (p.Pro1684Ser) |