| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| Y | g.12833779G>A | CA414999005 | USP9Y | c.5113G>A (p.Ala1705Thr) n.5125G>A c.4879G>A (p.Ala1627Thr) c.5128G>A (p.Ala1710Thr) | |
| Y | g.12833779G>C | CA414999007 | USP9Y | c.5113G>C (p.Ala1705Pro) n.5125G>C c.4879G>C (p.Ala1627Pro) c.5128G>C (p.Ala1710Pro) | |
| Y | g.12833779G= | CA2470560453 | USP9Y | c.5113G= (p.Ala1705=) n.5125G= c.4879G= (p.Ala1627=) c.5128G= (p.Ala1710=) | |
| Y | g.12833779G>T | CA337720911 | USP9Y | c.5113G>T (p.Ala1705Ser) n.5125G>T c.4879G>T (p.Ala1627Ser) c.5128G>T (p.Ala1710Ser) | dbSNP |
| Y | g.12833780C>A | CA414999009 | USP9Y | c.5114C>A (p.Ala1705Asp) n.5126C>A c.4880C>A (p.Ala1627Asp) c.5129C>A (p.Ala1710Asp) | |
| Y | g.12833780C>G | CA414999010 | USP9Y | c.5114C>G (p.Ala1705Gly) n.5126C>G c.4880C>G (p.Ala1627Gly) c.5129C>G (p.Ala1710Gly) | |
| Y | g.12833780C>T | CA414999011 | USP9Y | c.5114C>T (p.Ala1705Val) n.5126C>T c.4880C>T (p.Ala1627Val) c.5129C>T (p.Ala1710Val) | |
| Y | g.12833781T>A | CA519901772 | USP9Y | c.5115T>A (p.Ala1705=) n.5127T>A c.4881T>A (p.Ala1627=) c.5130T>A (p.Ala1710=) | |
| Y | g.12833781T>C | CA519901773 | USP9Y | c.5115T>C (p.Ala1705=) n.5127T>C c.4881T>C (p.Ala1627=) c.5130T>C (p.Ala1710=) | |
| Y | g.12833781T>G | CA519901776 | USP9Y | c.5115T>G (p.Ala1705=) n.5127T>G c.4881T>G (p.Ala1627=) c.5130T>G (p.Ala1710=) | |
| Y | g.12833782T>A | CA414999014 | USP9Y | c.5116T>A (p.Leu1706Ile) n.5128T>A c.4882T>A (p.Leu1628Ile) c.5131T>A (p.Leu1711Ile) | |
| Y | g.12833782T>C | CA519901781 | USP9Y | c.5116T>C (p.Leu1706=) n.5128T>C c.4882T>C (p.Leu1628=) c.5131T>C (p.Leu1711=) | |
| Y | g.12833782T>G | CA414999015 | USP9Y | c.5116T>G (p.Leu1706Val) n.5128T>G c.4882T>G (p.Leu1628Val) c.5131T>G (p.Leu1711Val) | |
| Y | g.12833783T>A | CA414999020 | USP9Y | c.5117T>A (p.Leu1706Ter) n.5129T>A c.4883T>A (p.Leu1628Ter) c.5132T>A (p.Leu1711Ter) | |
| Y | g.12833783T>C | CA414999017 | USP9Y | c.5117T>C (p.Leu1706Ser) n.5129T>C c.4883T>C (p.Leu1628Ser) c.5132T>C (p.Leu1711Ser) | |
| Y | g.12833783T>G | CA414999018 | USP9Y | c.5117T>G (p.Leu1706Ter) n.5129T>G c.4883T>G (p.Leu1628Ter) c.5132T>G (p.Leu1711Ter) | |
| Y | g.12833784A>C | CA414999022 | USP9Y | c.5118A>C (p.Leu1706Phe) n.5130A>C c.4884A>C (p.Leu1628Phe) c.5133A>C (p.Leu1711Phe) | |
| Y | g.12833784A>G | CA519901790 | USP9Y | c.5118A>G (p.Leu1706=) n.5130A>G c.4884A>G (p.Leu1628=) c.5133A>G (p.Leu1711=) | |
| Y | g.12833784A>T | CA414999023 | USP9Y | c.5118A>T (p.Leu1706Phe) n.5130A>T c.4884A>T (p.Leu1628Phe) c.5133A>T (p.Leu1711Phe) | |
| Y | g.12833785G>A | CA414999025 | USP9Y | c.5119G>A (p.Gly1707Arg) n.5131G>A c.4885G>A (p.Gly1629Arg) c.5134G>A (p.Gly1712Arg) | |
| Y | g.12833785G>C | CA414999027 | USP9Y | c.5119G>C (p.Gly1707Arg) n.5131G>C c.4885G>C (p.Gly1629Arg) c.5134G>C (p.Gly1712Arg) | |
| Y | g.12833785G>T | CA414999029 | USP9Y | c.5119G>T (p.Gly1707Ter) n.5131G>T c.4885G>T (p.Gly1629Ter) c.5134G>T (p.Gly1712Ter) | |
| Y | g.12833786G>A | CA414999030 | USP9Y | c.5120G>A (p.Gly1707Glu) n.5132G>A c.4886G>A (p.Gly1629Glu) c.5135G>A (p.Gly1712Glu) | |
| Y | g.12833786G>C | CA414999031 | USP9Y | c.5120G>C (p.Gly1707Ala) n.5132G>C c.4886G>C (p.Gly1629Ala) c.5135G>C (p.Gly1712Ala) | |
| Y | g.12833786G>T | CA414999033 | USP9Y | c.5120G>T (p.Gly1707Val) n.5132G>T c.4886G>T (p.Gly1629Val) c.5135G>T (p.Gly1712Val) | |
| Y | g.12833787A>C | CA519901801 | USP9Y | c.5121A>C (p.Gly1707=) n.5133A>C c.4887A>C (p.Gly1629=) c.5136A>C (p.Gly1712=) | |
| Y | g.12833787A>G | CA519901803 | USP9Y | c.5121A>G (p.Gly1707=) n.5133A>G c.4887A>G (p.Gly1629=) c.5136A>G (p.Gly1712=) | |
| Y | g.12833787A>T | CA519901805 | USP9Y | c.5121A>T (p.Gly1707=) n.5133A>T c.4887A>T (p.Gly1629=) c.5136A>T (p.Gly1712=) | |
| Y | g.12833788C>A | CA414999035 | USP9Y | c.5122C>A (p.His1708Asn) n.5134C>A c.4888C>A (p.His1630Asn) c.5137C>A (p.His1713Asn) | |
| Y | g.12833788C= | CA2470560454 | USP9Y | c.5122C= (p.His1708=) n.5134C= c.4888C= (p.His1630=) c.5137C= (p.His1713=) | |
| Y | g.12833788C>G | CA414999037 | USP9Y | c.5122C>G (p.His1708Asp) n.5134C>G c.4888C>G (p.His1630Asp) c.5137C>G (p.His1713Asp) | |
| Y | g.12833788C>T | CA414999038 | USP9Y | c.5122C>T (p.His1708Tyr) n.5134C>T c.4888C>T (p.His1630Tyr) c.5137C>T (p.His1713Tyr) | dbSNP gnomAD v2 |
| Y | g.12833789A>C | CA414999044 | USP9Y | c.5123A>C (p.His1708Pro) n.5135A>C c.4889A>C (p.His1630Pro) c.5138A>C (p.His1713Pro) | |
| Y | g.12833789A>G | CA414999042 | USP9Y | c.5123A>G (p.His1708Arg) n.5135A>G c.4889A>G (p.His1630Arg) c.5138A>G (p.His1713Arg) | |
| Y | g.12833789A>T | CA414999040 | USP9Y | c.5123A>T (p.His1708Leu) n.5135A>T c.4889A>T (p.His1630Leu) c.5138A>T (p.His1713Leu) | |
| Y | g.12833790C>A | CA414999045 | USP9Y | c.5124C>A (p.His1708Gln) n.5136C>A c.4890C>A (p.His1630Gln) c.5139C>A (p.His1713Gln) | |
| Y | g.12833790C>G | CA414999047 | USP9Y | c.5124C>G (p.His1708Gln) n.5136C>G c.4890C>G (p.His1630Gln) c.5139C>G (p.His1713Gln) | |
| Y | g.12833790C>T | CA519901815 | USP9Y | c.5124C>T (p.His1708=) n.5136C>T c.4890C>T (p.His1630=) c.5139C>T (p.His1713=) | |
| Y | g.12833791C>A | CA414999049 | USP9Y | c.5125C>A (p.Pro1709Thr) n.5137C>A c.4891C>A (p.Pro1631Thr) c.5140C>A (p.Pro1714Thr) | |
| Y | g.12833791C>G | CA414999051 | USP9Y | c.5125C>G (p.Pro1709Ala) n.5137C>G c.4891C>G (p.Pro1631Ala) c.5140C>G (p.Pro1714Ala) | |
| Y | g.12833791C>T | CA414999052 | USP9Y | c.5125C>T (p.Pro1709Ser) n.5137C>T c.4891C>T (p.Pro1631Ser) c.5140C>T (p.Pro1714Ser) | |
| Y | g.12833792C>A | CA414999054 | USP9Y | c.5126C>A (p.Pro1709Gln) n.5138C>A c.4892C>A (p.Pro1631Gln) c.5141C>A (p.Pro1714Gln) | |
| Y | g.12833792C>G | CA414999056 | USP9Y | c.5126C>G (p.Pro1709Arg) n.5138C>G c.4892C>G (p.Pro1631Arg) c.5141C>G (p.Pro1714Arg) | |
| Y | g.12833792C>T | CA414999057 | USP9Y | c.5126C>T (p.Pro1709Leu) n.5138C>T c.4892C>T (p.Pro1631Leu) c.5141C>T (p.Pro1714Leu) | |
| Y | g.12833793G>A | CA10573383 | USP9Y | c.5127G>A (p.Pro1709=) n.5139G>A c.4893G>A (p.Pro1631=) c.5142G>A (p.Pro1714=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| Y | g.12833793G>C | CA519901826 | USP9Y | c.5127G>C (p.Pro1709=) n.5139G>C c.4893G>C (p.Pro1631=) c.5142G>C (p.Pro1714=) | |
| Y | g.12833793G= | CA2470560455 | USP9Y | c.5127G= (p.Pro1709=) n.5139G= c.4893G= (p.Pro1631=) c.5142G= (p.Pro1714=) | |
| Y | g.12833793G>T | CA519901828 | USP9Y | c.5127G>T (p.Pro1709=) n.5139G>T c.4893G>T (p.Pro1631=) c.5142G>T (p.Pro1714=) | |
| Y | g.12833794G>A | CA414999060 | USP9Y | c.5128G>A (p.Ala1710Thr) n.5140G>A c.4894G>A (p.Ala1632Thr) c.5143G>A (p.Ala1715Thr) | |
| Y | g.12833794G>C | CA414999062 | USP9Y | c.5128G>C (p.Ala1710Pro) n.5140G>C c.4894G>C (p.Ala1632Pro) c.5143G>C (p.Ala1715Pro) |