| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.77942701G>A | CA340883147 | NEXN | c.1900G>A (p.Gly634Arg) c.1708G>A (p.Gly570Arg) c.1599G>A n.739G>A n.1474G>A c.1858G>A (p.Gly620Arg) c.1678G>A (p.Gly560Arg) c.1666G>A (p.Gly556Arg) c.1483G>A (p.Gly495Arg) | gnomAD v4 |
| 1 | g.77942701G>C | CA340883148 | NEXN | c.1900G>C (p.Gly634Arg) c.1708G>C (p.Gly570Arg) c.1599G>C n.739G>C n.1474G>C c.1858G>C (p.Gly620Arg) c.1678G>C (p.Gly560Arg) c.1666G>C (p.Gly556Arg) c.1483G>C (p.Gly495Arg) | |
| 1 | g.77942701G>T | CA340883149 | NEXN | c.1900G>T (p.Gly634Ter) c.1708G>T (p.Gly570Ter) c.1599G>T n.739G>T n.1474G>T c.1858G>T (p.Gly620Ter) c.1678G>T (p.Gly560Ter) c.1666G>T (p.Gly556Ter) c.1483G>T (p.Gly495Ter) | |
| 1 | g.77942701_77942705delinsGGAGA | CA1177631443 | NEXN | c.1900_1904delinsGGAGA (p.Gly634=) c.1708_1712delinsGGAGA (p.Gly570=) c.1599_1603delinsGGAGA n.739_743delinsGGAGA n.1474_1478delinsGGAGA c.1858_1862delinsGGAGA (p.Gly620=) c.1678_1682delinsGGAGA (p.Gly560=) c.1666_1670delinsGGAGA (p.Gly556=) c.1483_1487delinsGGAGA (p.Gly495=) | |
| 1 | g.77942702G>A | CA340883150 | NEXN | c.1901G>A (p.Gly634Glu) c.1709G>A (p.Gly570Glu) c.1600G>A n.740G>A n.1475G>A c.1859G>A (p.Gly620Glu) c.1679G>A (p.Gly560Glu) c.1667G>A (p.Gly556Glu) c.1484G>A (p.Gly495Glu) | |
| 1 | g.77942702G>C | CA340883151 | NEXN | c.1901G>C (p.Gly634Ala) c.1709G>C (p.Gly570Ala) c.1600G>C n.740G>C n.1475G>C c.1859G>C (p.Gly620Ala) c.1679G>C (p.Gly560Ala) c.1667G>C (p.Gly556Ala) c.1484G>C (p.Gly495Ala) | |
| 1 | g.77942702G>T | CA340883152 | NEXN | c.1901G>T (p.Gly634Val) c.1709G>T (p.Gly570Val) c.1600G>T n.740G>T n.1475G>T c.1859G>T (p.Gly620Val) c.1679G>T (p.Gly560Val) c.1667G>T (p.Gly556Val) c.1484G>T (p.Gly495Val) | |
| 1 | g.77942702_77942705delinsTCT | CA658795480 | NEXN | c.1901_1904delinsTCT (p.Gly634ValfsTer2) c.1709_1712delinsTCT (p.Gly570ValfsTer2) c.1600_1603delinsTCT n.740_743delinsTCT n.1475_1478delinsTCT c.1859_1862delinsTCT (p.Gly620ValfsTer2) c.1679_1682delinsTCT (p.Gly560ValfsTer2) c.1667_1670delinsTCT (p.Gly556ValfsTer2) c.1484_1487delinsTCT (p.Gly495ValfsTer2) | ClinVar dbSNP |
| 1 | g.77942703A= | CA1177631444 | NEXN | c.1902A= (p.Gly634=) c.1710A= (p.Gly570=) c.1601A= n.741A= n.1476A= c.1860A= (p.Gly620=) c.1680A= (p.Gly560=) c.1668A= (p.Gly556=) c.1485A= (p.Gly495=) | |
| 1 | g.77942703A>C | CA418709741 | NEXN | c.1902A>C (p.Gly634=) c.1710A>C (p.Gly570=) c.1601A>C n.741A>C n.1476A>C c.1860A>C (p.Gly620=) c.1680A>C (p.Gly560=) c.1668A>C (p.Gly556=) c.1485A>C (p.Gly495=) | |
| 1 | g.77942703A>G | CA418709742 | NEXN | c.1902A>G (p.Gly634=) c.1710A>G (p.Gly570=) c.1601A>G n.741A>G n.1476A>G c.1860A>G (p.Gly620=) c.1680A>G (p.Gly560=) c.1668A>G (p.Gly556=) c.1485A>G (p.Gly495=) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77942703A>T | CA418709743 | NEXN | c.1902A>T (p.Gly634=) c.1710A>T (p.Gly570=) c.1601A>T n.741A>T n.1476A>T c.1860A>T (p.Gly620=) c.1680A>T (p.Gly560=) c.1668A>T (p.Gly556=) c.1485A>T (p.Gly495=) | |
| 1 | g.77942704G>A | CA340883153 | NEXN | c.1903G>A (p.Glu635Lys) c.1711G>A (p.Glu571Lys) c.1602G>A n.742G>A n.1477G>A c.1861G>A (p.Glu621Lys) c.1681G>A (p.Glu561Lys) c.1669G>A (p.Glu557Lys) c.1486G>A (p.Glu496Lys) | gnomAD v4 |
| 1 | g.77942704G>C | CA340883154 | NEXN | c.1903G>C (p.Glu635Gln) c.1711G>C (p.Glu571Gln) c.1602G>C n.742G>C n.1477G>C c.1861G>C (p.Glu621Gln) c.1681G>C (p.Glu561Gln) c.1669G>C (p.Glu557Gln) c.1486G>C (p.Glu496Gln) | |
| 1 | g.77942704G>T | CA340883155 | NEXN | c.1903G>T (p.Glu635Ter) c.1711G>T (p.Glu571Ter) c.1602G>T n.742G>T n.1477G>T c.1861G>T (p.Glu621Ter) c.1681G>T (p.Glu561Ter) c.1669G>T (p.Glu557Ter) c.1486G>T (p.Glu496Ter) | |
| 1 | g.77942705A>C | CA340883158 | NEXN | c.1904A>C (p.Glu635Ala) c.1712A>C (p.Glu571Ala) c.1603A>C n.743A>C n.1478A>C c.1862A>C (p.Glu621Ala) c.1682A>C (p.Glu561Ala) c.1670A>C (p.Glu557Ala) c.1487A>C (p.Glu496Ala) | |
| 1 | g.77942705A>G | CA340883156 | NEXN | c.1904A>G (p.Glu635Gly) c.1712A>G (p.Glu571Gly) c.1603A>G n.743A>G n.1478A>G c.1862A>G (p.Glu621Gly) c.1682A>G (p.Glu561Gly) c.1670A>G (p.Glu557Gly) c.1487A>G (p.Glu496Gly) | |
| 1 | g.77942705A>T | CA340883157 | NEXN | c.1904A>T (p.Glu635Val) c.1712A>T (p.Glu571Val) c.1603A>T n.743A>T n.1478A>T c.1862A>T (p.Glu621Val) c.1682A>T (p.Glu561Val) c.1670A>T (p.Glu557Val) c.1487A>T (p.Glu496Val) | |
| 1 | g.77942706A>C | CA340883159 | NEXN | c.1905A>C (p.Glu635Asp) c.1713A>C (p.Glu571Asp) c.1604A>C n.744A>C n.1479A>C c.1863A>C (p.Glu621Asp) c.1683A>C (p.Glu561Asp) c.1671A>C (p.Glu557Asp) c.1488A>C (p.Glu496Asp) | COSMIC COSMIC |
| 1 | g.77942706A>G | CA418709745 | NEXN | c.1905A>G (p.Glu635=) c.1713A>G (p.Glu571=) c.1604A>G n.744A>G n.1479A>G c.1863A>G (p.Glu621=) c.1683A>G (p.Glu561=) c.1671A>G (p.Glu557=) c.1488A>G (p.Glu496=) | gnomAD v4 |
| 1 | g.77942706A>T | CA340883160 | NEXN | c.1905A>T (p.Glu635Asp) c.1713A>T (p.Glu571Asp) c.1604A>T n.744A>T n.1479A>T c.1863A>T (p.Glu621Asp) c.1683A>T (p.Glu561Asp) c.1671A>T (p.Glu557Asp) c.1488A>T (p.Glu496Asp) | |
| 1 | g.77942706_77942710delinsAACTT | CA1177631445 | NEXN | c.1905_1909delinsAACTT (p.Glu635=) c.1713_1717delinsAACTT (p.Glu571=) c.1604_1608delinsAACTT n.744_748delinsAACTT n.1479_1483delinsAACTT c.1863_1867delinsAACTT (p.Glu621=) c.1683_1687delinsAACTT (p.Glu561=) c.1671_1675delinsAACTT (p.Glu557=) c.1488_1492delinsAACTT (p.Glu496=) | |
| 1 | g.77942707A= | CA1177631446 | NEXN | c.1906A= (p.Thr636=) c.1714A= (p.Thr572=) c.1605A= n.745A= n.1480A= c.1864A= (p.Thr622=) c.1684A= (p.Thr562=) c.1672A= (p.Thr558=) c.1489A= (p.Thr497=) | |
| 1 | g.77942707A>C | CA340883161 | NEXN | c.1906A>C (p.Thr636Pro) c.1714A>C (p.Thr572Pro) c.1605A>C n.745A>C n.1480A>C c.1864A>C (p.Thr622Pro) c.1684A>C (p.Thr562Pro) c.1672A>C (p.Thr558Pro) c.1489A>C (p.Thr497Pro) | |
| 1 | g.77942707A>G | CA340883162 | NEXN | c.1906A>G (p.Thr636Ala) c.1714A>G (p.Thr572Ala) c.1605A>G n.745A>G n.1480A>G c.1864A>G (p.Thr622Ala) c.1684A>G (p.Thr562Ala) c.1672A>G (p.Thr558Ala) c.1489A>G (p.Thr497Ala) | |
| 1 | g.77942707A>T | CA919006 | NEXN | c.1906A>T (p.Thr636Ser) c.1714A>T (p.Thr572Ser) c.1605A>T n.745A>T n.1480A>T c.1864A>T (p.Thr622Ser) c.1684A>T (p.Thr562Ser) c.1672A>T (p.Thr558Ser) c.1489A>T (p.Thr497Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.77942710_77942713del | CA919005 | NEXN | c.1909_1912del (p.Tyr637AlafsTer?) c.1717_1720del (p.Tyr573AlafsTer?) c.1608_1611del n.748_751del n.1483_1486del c.1867_1870del (p.Tyr623AlafsTer?) c.1687_1690del (p.Tyr563AlafsTer?) c.1675_1678del (p.Tyr559AlafsTer?) c.1492_1495del (p.Tyr498AlafsTer?) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77942708C>A | CA340883163 | NEXN | c.1907C>A (p.Thr636Asn) c.1715C>A (p.Thr572Asn) c.1606C>A n.746C>A n.1481C>A c.1865C>A (p.Thr622Asn) c.1685C>A (p.Thr562Asn) c.1673C>A (p.Thr558Asn) c.1490C>A (p.Thr497Asn) | |
| 1 | g.77942708C>G | CA340883164 | NEXN | c.1907C>G (p.Thr636Ser) c.1715C>G (p.Thr572Ser) c.1606C>G n.746C>G n.1481C>G c.1865C>G (p.Thr622Ser) c.1685C>G (p.Thr562Ser) c.1673C>G (p.Thr558Ser) c.1490C>G (p.Thr497Ser) | |
| 1 | g.77942708C>T | CA340883165 | NEXN | c.1907C>T (p.Thr636Ile) c.1715C>T (p.Thr572Ile) c.1606C>T n.746C>T n.1481C>T c.1865C>T (p.Thr622Ile) c.1685C>T (p.Thr562Ile) c.1673C>T (p.Thr558Ile) c.1490C>T (p.Thr497Ile) | |
| 1 | g.77942709T>A | CA418709749 | NEXN | c.1908T>A (p.Thr636=) c.1716T>A (p.Thr572=) c.1607T>A n.747T>A n.1482T>A c.1866T>A (p.Thr622=) c.1686T>A (p.Thr562=) c.1674T>A (p.Thr558=) c.1491T>A (p.Thr497=) | |
| 1 | g.77942709T>C | CA418709750 | NEXN | c.1908T>C (p.Thr636=) c.1716T>C (p.Thr572=) c.1607T>C n.747T>C n.1482T>C c.1866T>C (p.Thr622=) c.1686T>C (p.Thr562=) c.1674T>C (p.Thr558=) c.1491T>C (p.Thr497=) | |
| 1 | g.77942709T>G | CA418709751 | NEXN | c.1908T>G (p.Thr636=) c.1716T>G (p.Thr572=) c.1607T>G n.747T>G n.1482T>G c.1866T>G (p.Thr622=) c.1686T>G (p.Thr562=) c.1674T>G (p.Thr558=) c.1491T>G (p.Thr497=) | gnomAD v4 |
| 1 | g.77942710T>A | CA340883166 | NEXN | c.1909T>A (p.Tyr637Asn) c.1717T>A (p.Tyr573Asn) c.1608T>A n.748T>A n.1483T>A c.1867T>A (p.Tyr623Asn) c.1687T>A (p.Tyr563Asn) c.1675T>A (p.Tyr559Asn) c.1492T>A (p.Tyr498Asn) | |
| 1 | g.77942710T>C | CA340883167 | NEXN | c.1909T>C (p.Tyr637His) c.1717T>C (p.Tyr573His) c.1608T>C n.748T>C n.1483T>C c.1867T>C (p.Tyr623His) c.1687T>C (p.Tyr563His) c.1675T>C (p.Tyr559His) c.1492T>C (p.Tyr498His) | |
| 1 | g.77942710T>G | CA340883168 | NEXN | c.1909T>G (p.Tyr637Asp) c.1717T>G (p.Tyr573Asp) c.1608T>G n.748T>G n.1483T>G c.1867T>G (p.Tyr623Asp) c.1687T>G (p.Tyr563Asp) c.1675T>G (p.Tyr559Asp) c.1492T>G (p.Tyr498Asp) | |
| 1 | g.77942711A>C | CA340883170 | NEXN | c.1910A>C (p.Tyr637Ser) c.1718A>C (p.Tyr573Ser) c.1609A>C n.749A>C n.1484A>C c.1868A>C (p.Tyr623Ser) c.1688A>C (p.Tyr563Ser) c.1676A>C (p.Tyr559Ser) c.1493A>C (p.Tyr498Ser) | |
| 1 | g.77942711A>G | CA340883171 | NEXN | c.1910A>G (p.Tyr637Cys) c.1718A>G (p.Tyr573Cys) c.1609A>G n.749A>G n.1484A>G c.1868A>G (p.Tyr623Cys) c.1688A>G (p.Tyr563Cys) c.1676A>G (p.Tyr559Cys) c.1493A>G (p.Tyr498Cys) | |
| 1 | g.77942711A>T | CA340883169 | NEXN | c.1910A>T (p.Tyr637Phe) c.1718A>T (p.Tyr573Phe) c.1609A>T n.749A>T n.1484A>T c.1868A>T (p.Tyr623Phe) c.1688A>T (p.Tyr563Phe) c.1676A>T (p.Tyr559Phe) c.1493A>T (p.Tyr498Phe) | |
| 1 | g.77942712C>A | CA335439 | NEXN | c.1911C>A (p.Tyr637Ter) c.1719C>A (p.Tyr573Ter) c.1610C>A n.750C>A n.1485C>A c.1869C>A (p.Tyr623Ter) c.1689C>A (p.Tyr563Ter) c.1677C>A (p.Tyr559Ter) c.1494C>A (p.Tyr498Ter) | ClinVar dbSNP |
| 1 | g.77942712C= | CA1177631447 | NEXN | c.1911C= (p.Tyr637=) c.1719C= (p.Tyr573=) c.1610C= n.750C= n.1485C= c.1869C= (p.Tyr623=) c.1689C= (p.Tyr563=) c.1677C= (p.Tyr559=) c.1494C= (p.Tyr498=) | |
| 1 | g.77942712C>G | CA340883172 | NEXN | c.1911C>G (p.Tyr637Ter) c.1719C>G (p.Tyr573Ter) c.1610C>G n.750C>G n.1485C>G c.1869C>G (p.Tyr623Ter) c.1689C>G (p.Tyr563Ter) c.1677C>G (p.Tyr559Ter) c.1494C>G (p.Tyr498Ter) | |
| 1 | g.77942712C>T | CA919007 | NEXN | c.1911C>T (p.Tyr637=) c.1719C>T (p.Tyr573=) c.1610C>T n.750C>T n.1485C>T c.1869C>T (p.Tyr623=) c.1689C>T (p.Tyr563=) c.1677C>T (p.Tyr559=) c.1494C>T (p.Tyr498=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.77942713T>A | CA340883173 | NEXN | c.1912T>A (p.Cys638Ser) c.1720T>A (p.Cys574Ser) c.1611T>A n.751T>A n.1486T>A c.1870T>A (p.Cys624Ser) c.1690T>A (p.Cys564Ser) c.1678T>A (p.Cys560Ser) c.1495T>A (p.Cys499Ser) | |
| 1 | g.77942713T>C | CA340883174 | NEXN | c.1912T>C (p.Cys638Arg) c.1720T>C (p.Cys574Arg) c.1611T>C n.751T>C n.1486T>C c.1870T>C (p.Cys624Arg) c.1690T>C (p.Cys564Arg) c.1678T>C (p.Cys560Arg) c.1495T>C (p.Cys499Arg) | |
| 1 | g.77942713T>G | CA340883175 | NEXN | c.1912T>G (p.Cys638Gly) c.1720T>G (p.Cys574Gly) c.1611T>G n.751T>G n.1486T>G c.1870T>G (p.Cys624Gly) c.1690T>G (p.Cys564Gly) c.1678T>G (p.Cys560Gly) c.1495T>G (p.Cys499Gly) | |
| 1 | g.77942714G>A | CA340883176 | NEXN | c.1913G>A (p.Cys638Tyr) c.1721G>A (p.Cys574Tyr) c.1612G>A n.752G>A n.1487G>A c.1871G>A (p.Cys624Tyr) c.1691G>A (p.Cys564Tyr) c.1679G>A (p.Cys560Tyr) c.1496G>A (p.Cys499Tyr) | |
| 1 | g.77942714G>C | CA340883177 | NEXN | c.1913G>C (p.Cys638Ser) c.1721G>C (p.Cys574Ser) c.1612G>C n.752G>C n.1487G>C c.1871G>C (p.Cys624Ser) c.1691G>C (p.Cys564Ser) c.1679G>C (p.Cys560Ser) c.1496G>C (p.Cys499Ser) | |
| 1 | g.77942714G>T | CA340883178 | NEXN | c.1913G>T (p.Cys638Phe) c.1721G>T (p.Cys574Phe) c.1612G>T n.752G>T n.1487G>T c.1871G>T (p.Cys624Phe) c.1691G>T (p.Cys564Phe) c.1679G>T (p.Cys560Phe) c.1496G>T (p.Cys499Phe) | |
| 1 | g.77942715C>A | CA340883179 | NEXN | c.1914C>A (p.Cys638Ter) c.1722C>A (p.Cys574Ter) c.1613C>A n.753C>A n.1488C>A c.1872C>A (p.Cys624Ter) c.1692C>A (p.Cys564Ter) c.1680C>A (p.Cys560Ter) c.1497C>A (p.Cys499Ter) | |
| 1 | g.77942715C>G | CA340883180 | NEXN | c.1914C>G (p.Cys638Trp) c.1722C>G (p.Cys574Trp) c.1613C>G n.753C>G n.1488C>G c.1872C>G (p.Cys624Trp) c.1692C>G (p.Cys564Trp) c.1680C>G (p.Cys560Trp) c.1497C>G (p.Cys499Trp) | |
| 1 | g.77942715C>T | CA418709758 | NEXN | c.1914C>T (p.Cys638=) c.1722C>T (p.Cys574=) c.1613C>T n.753C>T n.1488C>T c.1872C>T (p.Cys624=) c.1692C>T (p.Cys564=) c.1680C>T (p.Cys560=) c.1497C>T (p.Cys499=) | |
| 1 | g.77942716del | CA2646275683 | NEXN | c.1915del (p.Leu639PhefsTer?) c.1723del (p.Leu575PhefsTer?) c.1614del n.754del n.1489del c.1873del (p.Leu625PhefsTer?) c.1693del (p.Leu565PhefsTer?) c.1681del (p.Leu561PhefsTer?) c.1498del (p.Leu500PhefsTer?) | gnomAD v4 |
| 1 | g.77942715_77942720delinsCCTTTA | CA1177631448 | NEXN | c.1914_1919delinsCCTTTA (p.Cys638=) c.1722_1727delinsCCTTTA (p.Cys574=) c.1613_1618delinsCCTTTA n.753_758delinsCCTTTA n.1488_1493delinsCCTTTA c.1872_1877delinsCCTTTA (p.Cys624=) c.1692_1697delinsCCTTTA (p.Cys564=) c.1680_1685delinsCCTTTA (p.Cys560=) c.1497_1502delinsCCTTTA (p.Cys499=) | |
| 1 | g.77942716C>A | CA340883181 | NEXN | c.1915C>A (p.Leu639Ile) c.1723C>A (p.Leu575Ile) c.1614C>A n.754C>A n.1489C>A c.1873C>A (p.Leu625Ile) c.1693C>A (p.Leu565Ile) c.1681C>A (p.Leu561Ile) c.1498C>A (p.Leu500Ile) | |
| 1 | g.77942716C>G | CA340883182 | NEXN | c.1915C>G (p.Leu639Val) c.1723C>G (p.Leu575Val) c.1614C>G n.754C>G n.1489C>G c.1873C>G (p.Leu625Val) c.1693C>G (p.Leu565Val) c.1681C>G (p.Leu561Val) c.1498C>G (p.Leu500Val) | |
| 1 | g.77942716C>T | CA340883183 | NEXN | c.1915C>T (p.Leu639Phe) c.1723C>T (p.Leu575Phe) c.1614C>T n.754C>T n.1489C>T c.1873C>T (p.Leu625Phe) c.1693C>T (p.Leu565Phe) c.1681C>T (p.Leu561Phe) c.1498C>T (p.Leu500Phe) | |
| 1 | g.77942719_77942723del | CA658656943 | NEXN | c.1918_1922del (p.Tyr640ThrfsTer14) c.1726_1730del (p.Tyr576ThrfsTer14) c.1617_1621del n.757_761del n.1492_1496del c.1876_1880del (p.Tyr626ThrfsTer14) c.1696_1700del (p.Tyr566ThrfsTer14) c.1684_1688del (p.Tyr562ThrfsTer14) c.1501_1505del (p.Tyr501ThrfsTer14) | ClinVar dbSNP gnomAD v4 |
| 1 | g.77942717T>A | CA340883186 | NEXN | c.1916T>A (p.Leu639His) c.1724T>A (p.Leu575His) c.1615T>A n.755T>A n.1490T>A c.1874T>A (p.Leu625His) c.1694T>A (p.Leu565His) c.1682T>A (p.Leu561His) c.1499T>A (p.Leu500His) | |
| 1 | g.77942717T>C | CA340883184 | NEXN | c.1916T>C (p.Leu639Pro) c.1724T>C (p.Leu575Pro) c.1615T>C n.755T>C n.1490T>C c.1874T>C (p.Leu625Pro) c.1694T>C (p.Leu565Pro) c.1682T>C (p.Leu561Pro) c.1499T>C (p.Leu500Pro) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.77942717T>G | CA340883185 | NEXN | c.1916T>G (p.Leu639Arg) c.1724T>G (p.Leu575Arg) c.1615T>G n.755T>G n.1490T>G c.1874T>G (p.Leu625Arg) c.1694T>G (p.Leu565Arg) c.1682T>G (p.Leu561Arg) c.1499T>G (p.Leu500Arg) | |
| 1 | g.77942717T= | CA1177631449 | NEXN | c.1916T= (p.Leu639=) c.1724T= (p.Leu575=) c.1615T= n.755T= n.1490T= c.1874T= (p.Leu625=) c.1694T= (p.Leu565=) c.1682T= (p.Leu561=) c.1499T= (p.Leu500=) | |
| 1 | g.77942718T>A | CA418709760 | NEXN | c.1917T>A (p.Leu639=) c.1725T>A (p.Leu575=) c.1616T>A n.756T>A n.1491T>A c.1875T>A (p.Leu625=) c.1695T>A (p.Leu565=) c.1683T>A (p.Leu561=) c.1500T>A (p.Leu500=) | |
| 1 | g.77942718T>C | CA418709762 | NEXN | c.1917T>C (p.Leu639=) c.1725T>C (p.Leu575=) c.1616T>C n.756T>C n.1491T>C c.1875T>C (p.Leu625=) c.1695T>C (p.Leu565=) c.1683T>C (p.Leu561=) c.1500T>C (p.Leu500=) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77942718T>G | CA418709763 | NEXN | c.1917T>G (p.Leu639=) c.1725T>G (p.Leu575=) c.1616T>G n.756T>G n.1491T>G c.1875T>G (p.Leu625=) c.1695T>G (p.Leu565=) c.1683T>G (p.Leu561=) c.1500T>G (p.Leu500=) | |
| 1 | g.77942718T= | CA1177631450 | NEXN | c.1917T= (p.Leu639=) c.1725T= (p.Leu575=) c.1616T= n.756T= n.1491T= c.1875T= (p.Leu625=) c.1695T= (p.Leu565=) c.1683T= (p.Leu561=) c.1500T= (p.Leu500=) | |
| 1 | g.77942719T>A | CA340883187 | NEXN | c.1918T>A (p.Tyr640Asn) c.1726T>A (p.Tyr576Asn) c.1617T>A n.757T>A n.1492T>A c.1876T>A (p.Tyr626Asn) c.1696T>A (p.Tyr566Asn) c.1684T>A (p.Tyr562Asn) c.1501T>A (p.Tyr501Asn) | |
| 1 | g.77942719T>C | CA340883188 | NEXN | c.1918T>C (p.Tyr640His) c.1726T>C (p.Tyr576His) c.1617T>C n.757T>C n.1492T>C c.1876T>C (p.Tyr626His) c.1696T>C (p.Tyr566His) c.1684T>C (p.Tyr562His) c.1501T>C (p.Tyr501His) | |
| 1 | g.77942719T>G | CA340883189 | NEXN | c.1918T>G (p.Tyr640Asp) c.1726T>G (p.Tyr576Asp) c.1617T>G n.757T>G n.1492T>G c.1876T>G (p.Tyr626Asp) c.1696T>G (p.Tyr566Asp) c.1684T>G (p.Tyr562Asp) c.1501T>G (p.Tyr501Asp) | |
| 1 | g.77942720A>C | CA340883190 | NEXN | c.1919A>C (p.Tyr640Ser) c.1727A>C (p.Tyr576Ser) c.1618A>C n.758A>C n.1493A>C c.1877A>C (p.Tyr626Ser) c.1697A>C (p.Tyr566Ser) c.1685A>C (p.Tyr562Ser) c.1502A>C (p.Tyr501Ser) | |
| 1 | g.77942720A>G | CA340883191 | NEXN | c.1919A>G (p.Tyr640Cys) c.1727A>G (p.Tyr576Cys) c.1618A>G n.758A>G n.1493A>G c.1877A>G (p.Tyr626Cys) c.1697A>G (p.Tyr566Cys) c.1685A>G (p.Tyr562Cys) c.1502A>G (p.Tyr501Cys) | COSMIC COSMIC |
| 1 | g.77942720A>T | CA340883192 | NEXN | c.1919A>T (p.Tyr640Phe) c.1727A>T (p.Tyr576Phe) c.1618A>T n.758A>T n.1493A>T c.1877A>T (p.Tyr626Phe) c.1697A>T (p.Tyr566Phe) c.1685A>T (p.Tyr562Phe) c.1502A>T (p.Tyr501Phe) | |
| 1 | g.77942721C>A | CA340883193 | NEXN | c.1920C>A (p.Tyr640Ter) c.1728C>A (p.Tyr576Ter) c.1619C>A n.759C>A n.1494C>A c.1878C>A (p.Tyr626Ter) c.1698C>A (p.Tyr566Ter) c.1686C>A (p.Tyr562Ter) c.1503C>A (p.Tyr501Ter) | |
| 1 | g.77942721C>G | CA340883194 | NEXN | c.1920C>G (p.Tyr640Ter) c.1728C>G (p.Tyr576Ter) c.1619C>G n.759C>G n.1494C>G c.1878C>G (p.Tyr626Ter) c.1698C>G (p.Tyr566Ter) c.1686C>G (p.Tyr562Ter) c.1503C>G (p.Tyr501Ter) | |
| 1 | g.77942721C>T | CA418709765 | NEXN | c.1920C>T (p.Tyr640=) c.1728C>T (p.Tyr576=) c.1619C>T n.759C>T n.1494C>T c.1878C>T (p.Tyr626=) c.1698C>T (p.Tyr566=) c.1686C>T (p.Tyr562=) c.1503C>T (p.Tyr501=) | |
| 1 | g.77942722T>A | CA340883195 | NEXN | c.1921T>A (p.Leu641Ile) c.1729T>A (p.Leu577Ile) c.1620T>A n.760T>A n.1495T>A c.1879T>A (p.Leu627Ile) c.1699T>A (p.Leu567Ile) c.1687T>A (p.Leu563Ile) c.1504T>A (p.Leu502Ile) | |
| 1 | g.77942722T>C | CA418709767 | NEXN | c.1921T>C (p.Leu641=) c.1729T>C (p.Leu577=) c.1620T>C n.760T>C n.1495T>C c.1879T>C (p.Leu627=) c.1699T>C (p.Leu567=) c.1687T>C (p.Leu563=) c.1504T>C (p.Leu502=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77942722T>G | CA340883196 | NEXN | c.1921T>G (p.Leu641Val) c.1729T>G (p.Leu577Val) c.1620T>G n.760T>G n.1495T>G c.1879T>G (p.Leu627Val) c.1699T>G (p.Leu567Val) c.1687T>G (p.Leu563Val) c.1504T>G (p.Leu502Val) | gnomAD v4 |
| 1 | g.77942722T= | CA1177631451 | NEXN | c.1921T= (p.Leu641=) c.1729T= (p.Leu577=) c.1620T= n.760T= n.1495T= c.1879T= (p.Leu627=) c.1699T= (p.Leu567=) c.1687T= (p.Leu563=) c.1504T= (p.Leu502=) | |
| 1 | g.77942723T>A | CA340883197 | NEXN | c.1922T>A (p.Leu641Ter) c.1730T>A (p.Leu577Ter) c.1621T>A n.761T>A n.1496T>A c.1880T>A (p.Leu627Ter) c.1700T>A (p.Leu567Ter) c.1688T>A (p.Leu563Ter) c.1505T>A (p.Leu502Ter) | |
| 1 | g.77942723T>C | CA919008 | NEXN | c.1922T>C (p.Leu641Ser) c.1730T>C (p.Leu577Ser) c.1621T>C n.761T>C n.1496T>C c.1880T>C (p.Leu627Ser) c.1700T>C (p.Leu567Ser) c.1688T>C (p.Leu563Ser) c.1505T>C (p.Leu502Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.77942723T>G | CA340883198 | NEXN | c.1922T>G (p.Leu641Ter) c.1730T>G (p.Leu577Ter) c.1621T>G n.761T>G n.1496T>G c.1880T>G (p.Leu627Ter) c.1700T>G (p.Leu567Ter) c.1688T>G (p.Leu563Ter) c.1505T>G (p.Leu502Ter) | ClinVar |
| 1 | g.77942723T= | CA1177631452 | NEXN | c.1922T= (p.Leu641=) c.1730T= (p.Leu577=) c.1621T= n.761T= n.1496T= c.1880T= (p.Leu627=) c.1700T= (p.Leu567=) c.1688T= (p.Leu563=) c.1505T= (p.Leu502=) | |
| 1 | g.77942724A>C | CA340883199 | NEXN | c.1923A>C (p.Leu641Phe) c.1731A>C (p.Leu577Phe) c.1622A>C n.762A>C n.1497A>C c.1881A>C (p.Leu627Phe) c.1701A>C (p.Leu567Phe) c.1689A>C (p.Leu563Phe) c.1506A>C (p.Leu502Phe) | |
| 1 | g.77942724A>G | CA418709771 | NEXN | c.1923A>G (p.Leu641=) c.1731A>G (p.Leu577=) c.1622A>G n.762A>G n.1497A>G c.1881A>G (p.Leu627=) c.1701A>G (p.Leu567=) c.1689A>G (p.Leu563=) c.1506A>G (p.Leu502=) | |
| 1 | g.77942724A>T | CA340883200 | NEXN | c.1923A>T (p.Leu641Phe) c.1731A>T (p.Leu577Phe) c.1622A>T n.762A>T n.1497A>T c.1881A>T (p.Leu627Phe) c.1701A>T (p.Leu567Phe) c.1689A>T (p.Leu563Phe) c.1506A>T (p.Leu502Phe) | |
| 1 | g.77942725C>A | CA340883201 | NEXN | c.1924C>A (p.Pro642Thr) c.1732C>A (p.Pro578Thr) c.1623C>A n.763C>A n.1498C>A c.1882C>A (p.Pro628Thr) c.1702C>A (p.Pro568Thr) c.1690C>A (p.Pro564Thr) c.1507C>A (p.Pro503Thr) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.77942725C= | CA1177631453 | NEXN | c.1924C= (p.Pro642=) c.1732C= (p.Pro578=) c.1623C= n.763C= n.1498C= c.1882C= (p.Pro628=) c.1702C= (p.Pro568=) c.1690C= (p.Pro564=) c.1507C= (p.Pro503=) | |
| 1 | g.77942725C>G | CA340883202 | NEXN | c.1924C>G (p.Pro642Ala) c.1732C>G (p.Pro578Ala) c.1623C>G n.763C>G n.1498C>G c.1882C>G (p.Pro628Ala) c.1702C>G (p.Pro568Ala) c.1690C>G (p.Pro564Ala) c.1507C>G (p.Pro503Ala) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77942725C>T | CA340883203 | NEXN | c.1924C>T (p.Pro642Ser) c.1732C>T (p.Pro578Ser) c.1623C>T n.763C>T n.1498C>T c.1882C>T (p.Pro628Ser) c.1702C>T (p.Pro568Ser) c.1690C>T (p.Pro564Ser) c.1507C>T (p.Pro503Ser) | dbSNP gnomAD v4 |
| 1 | g.77942726C>A | CA340883204 | NEXN | c.1925C>A (p.Pro642Gln) c.1733C>A (p.Pro578Gln) c.1624C>A n.764C>A n.1499C>A c.1883C>A (p.Pro628Gln) c.1703C>A (p.Pro568Gln) c.1691C>A (p.Pro564Gln) c.1508C>A (p.Pro503Gln) | gnomAD v4 |
| 1 | g.77942726C>G | CA16622160 | NEXN | c.1925C>G (p.Pro642Arg) c.1733C>G (p.Pro578Arg) c.1624C>G n.764C>G n.1499C>G c.1883C>G (p.Pro628Arg) c.1703C>G (p.Pro568Arg) c.1691C>G (p.Pro564Arg) c.1508C>G (p.Pro503Arg) | gnomAD v4 |
| 1 | g.77942726C>T | CA340883205 | NEXN | c.1925C>T (p.Pro642Leu) c.1733C>T (p.Pro578Leu) c.1624C>T n.764C>T n.1499C>T c.1883C>T (p.Pro628Leu) c.1703C>T (p.Pro568Leu) c.1691C>T (p.Pro564Leu) c.1508C>T (p.Pro503Leu) | |
| 1 | g.77942727A>C | CA418709772 | NEXN | c.1926A>C (p.Pro642=) c.1734A>C (p.Pro578=) c.1625A>C n.765A>C n.1500A>C c.1884A>C (p.Pro628=) c.1704A>C (p.Pro568=) c.1692A>C (p.Pro564=) c.1509A>C (p.Pro503=) | |
| 1 | g.77942727A>G | CA418709776 | NEXN | c.1926A>G (p.Pro642=) c.1734A>G (p.Pro578=) c.1625A>G n.765A>G n.1500A>G c.1884A>G (p.Pro628=) c.1704A>G (p.Pro568=) c.1692A>G (p.Pro564=) c.1509A>G (p.Pro503=) | |
| 1 | g.77942727A>T | CA418709774 | NEXN | c.1926A>T (p.Pro642=) c.1734A>T (p.Pro578=) c.1625A>T n.765A>T n.1500A>T c.1884A>T (p.Pro628=) c.1704A>T (p.Pro568=) c.1692A>T (p.Pro564=) c.1509A>T (p.Pro503=) | |
| 1 | g.77942728G>A | CA340883208 | NEXN | c.1927G>A (p.Glu643Lys) c.1735G>A (p.Glu579Lys) c.1626G>A n.766G>A n.1501G>A c.1885G>A (p.Glu629Lys) c.1705G>A (p.Glu569Lys) c.1693G>A (p.Glu565Lys) c.1510G>A (p.Glu504Lys) | |
| 1 | g.77942728G>C | CA340883206 | NEXN | c.1927G>C (p.Glu643Gln) c.1735G>C (p.Glu579Gln) c.1626G>C n.766G>C n.1501G>C c.1885G>C (p.Glu629Gln) c.1705G>C (p.Glu569Gln) c.1693G>C (p.Glu565Gln) c.1510G>C (p.Glu504Gln) | |
| 1 | g.77942728G>T | CA340883207 | NEXN | c.1927G>T (p.Glu643Ter) c.1735G>T (p.Glu579Ter) c.1626G>T n.766G>T n.1501G>T c.1885G>T (p.Glu629Ter) c.1705G>T (p.Glu569Ter) c.1693G>T (p.Glu565Ter) c.1510G>T (p.Glu504Ter) | |
| 1 | g.77942729A= | CA1177631454 | NEXN | c.1928A= (p.Glu643=) c.1736A= (p.Glu579=) c.1627A= n.767A= n.1502A= c.1886A= (p.Glu629=) c.1706A= (p.Glu569=) c.1694A= (p.Glu565=) c.1511A= (p.Glu504=) | |
| 1 | g.77942729A>C | CA340883209 | NEXN | c.1928A>C (p.Glu643Ala) c.1736A>C (p.Glu579Ala) c.1627A>C n.767A>C n.1502A>C c.1886A>C (p.Glu629Ala) c.1706A>C (p.Glu569Ala) c.1694A>C (p.Glu565Ala) c.1511A>C (p.Glu504Ala) | ClinVar dbSNP gnomAD v4 |
| 1 | g.77942729A>G | CA340883210 | NEXN | c.1928A>G (p.Glu643Gly) c.1736A>G (p.Glu579Gly) c.1627A>G n.767A>G n.1502A>G c.1886A>G (p.Glu629Gly) c.1706A>G (p.Glu569Gly) c.1694A>G (p.Glu565Gly) c.1511A>G (p.Glu504Gly) | |
| 1 | g.77942729A>T | CA340883211 | NEXN | c.1928A>T (p.Glu643Val) c.1736A>T (p.Glu579Val) c.1627A>T n.767A>T n.1502A>T c.1886A>T (p.Glu629Val) c.1706A>T (p.Glu569Val) c.1694A>T (p.Glu565Val) c.1511A>T (p.Glu504Val) | gnomAD v4 |
| 1 | g.77942731del | CA2580063261 | NEXN | c.1930del (p.Thr644LeufsTer?) c.1738del (p.Thr580LeufsTer?) c.1629del n.769del n.1504del c.1888del (p.Thr630LeufsTer?) c.1708del (p.Thr570LeufsTer?) c.1696del (p.Thr566LeufsTer?) c.1513del (p.Thr505LeufsTer?) | ClinVar |
| 1 | g.77942730A>C | CA340883212 | NEXN | c.1929A>C (p.Glu643Asp) c.1737A>C (p.Glu579Asp) c.1628A>C n.768A>C n.1503A>C c.1887A>C (p.Glu629Asp) c.1707A>C (p.Glu569Asp) c.1695A>C (p.Glu565Asp) c.1512A>C (p.Glu504Asp) | gnomAD v4 |
| 1 | g.77942730A>G | CA418709779 | NEXN | c.1929A>G (p.Glu643=) c.1737A>G (p.Glu579=) c.1628A>G n.768A>G n.1503A>G c.1887A>G (p.Glu629=) c.1707A>G (p.Glu569=) c.1695A>G (p.Glu565=) c.1512A>G (p.Glu504=) | |
| 1 | g.77942730A>T | CA340883213 | NEXN | c.1929A>T (p.Glu643Asp) c.1737A>T (p.Glu579Asp) c.1628A>T n.768A>T n.1503A>T c.1887A>T (p.Glu629Asp) c.1707A>T (p.Glu569Asp) c.1695A>T (p.Glu565Asp) c.1512A>T (p.Glu504Asp) | |
| 1 | g.77942731A>C | CA340883214 | NEXN | c.1930A>C (p.Thr644Pro) c.1738A>C (p.Thr580Pro) c.1629A>C n.769A>C n.1504A>C c.1888A>C (p.Thr630Pro) c.1708A>C (p.Thr570Pro) c.1696A>C (p.Thr566Pro) c.1513A>C (p.Thr505Pro) | |
| 1 | g.77942731A>G | CA340883216 | NEXN | c.1930A>G (p.Thr644Ala) c.1738A>G (p.Thr580Ala) c.1629A>G n.769A>G n.1504A>G c.1888A>G (p.Thr630Ala) c.1708A>G (p.Thr570Ala) c.1696A>G (p.Thr566Ala) c.1513A>G (p.Thr505Ala) | gnomAD v4 |
| 1 | g.77942731A>T | CA340883215 | NEXN | c.1930A>T (p.Thr644Ser) c.1738A>T (p.Thr580Ser) c.1629A>T n.769A>T n.1504A>T c.1888A>T (p.Thr630Ser) c.1708A>T (p.Thr570Ser) c.1696A>T (p.Thr566Ser) c.1513A>T (p.Thr505Ser) | |
| 1 | g.77942732C>A | CA340883217 | NEXN | c.1931C>A (p.Thr644Asn) c.1739C>A (p.Thr580Asn) c.1630C>A n.770C>A n.1505C>A c.1889C>A (p.Thr630Asn) c.1709C>A (p.Thr570Asn) c.1697C>A (p.Thr566Asn) c.1514C>A (p.Thr505Asn) | |
| 1 | g.77942732C>G | CA340883218 | NEXN | c.1931C>G (p.Thr644Ser) c.1739C>G (p.Thr580Ser) c.1630C>G n.770C>G n.1505C>G c.1889C>G (p.Thr630Ser) c.1709C>G (p.Thr570Ser) c.1697C>G (p.Thr566Ser) c.1514C>G (p.Thr505Ser) | |
| 1 | g.77942732C>T | CA340883219 | NEXN | c.1931C>T (p.Thr644Ile) c.1739C>T (p.Thr580Ile) c.1630C>T n.770C>T n.1505C>T c.1889C>T (p.Thr630Ile) c.1709C>T (p.Thr570Ile) c.1697C>T (p.Thr566Ile) c.1514C>T (p.Thr505Ile) | |
| 1 | g.77942733T>A | CA418709786 | NEXN | c.1932T>A (p.Thr644=) c.1740T>A (p.Thr580=) c.1631T>A n.771T>A n.1506T>A c.1890T>A (p.Thr630=) c.1710T>A (p.Thr570=) c.1698T>A (p.Thr566=) c.1515T>A (p.Thr505=) | |
| 1 | g.77942733T>C | CA418709787 | NEXN | c.1932T>C (p.Thr644=) c.1740T>C (p.Thr580=) c.1631T>C n.771T>C n.1506T>C c.1890T>C (p.Thr630=) c.1710T>C (p.Thr570=) c.1698T>C (p.Thr566=) c.1515T>C (p.Thr505=) | dbSNP gnomAD v4 |
| 1 | g.77942733T>G | CA418709788 | NEXN | c.1932T>G (p.Thr644=) c.1740T>G (p.Thr580=) c.1631T>G n.771T>G n.1506T>G c.1890T>G (p.Thr630=) c.1710T>G (p.Thr570=) c.1698T>G (p.Thr566=) c.1515T>G (p.Thr505=) | |
| 1 | g.77942733T= | CA1177631455 | NEXN | c.1932T= (p.Thr644=) c.1740T= (p.Thr580=) c.1631T= n.771T= n.1506T= c.1890T= (p.Thr630=) c.1710T= (p.Thr570=) c.1698T= (p.Thr566=) c.1515T= (p.Thr505=) | |
| 1 | g.77942734T>A | CA340883220 | NEXN | c.1933T>A (p.Phe645Ile) c.1741T>A (p.Phe581Ile) c.1632T>A n.772T>A n.1507T>A c.1891T>A (p.Phe631Ile) c.1711T>A (p.Phe571Ile) c.1699T>A (p.Phe567Ile) c.1516T>A (p.Phe506Ile) | |
| 1 | g.77942734T>C | CA340883221 | NEXN | c.1933T>C (p.Phe645Leu) c.1741T>C (p.Phe581Leu) c.1632T>C n.772T>C n.1507T>C c.1891T>C (p.Phe631Leu) c.1711T>C (p.Phe571Leu) c.1699T>C (p.Phe567Leu) c.1516T>C (p.Phe506Leu) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 1 | g.77942734T>G | CA340883222 | NEXN | c.1933T>G (p.Phe645Val) c.1741T>G (p.Phe581Val) c.1632T>G n.772T>G n.1507T>G c.1891T>G (p.Phe631Val) c.1711T>G (p.Phe571Val) c.1699T>G (p.Phe567Val) c.1516T>G (p.Phe506Val) | |
| 1 | g.77942734T= | CA1177631456 | NEXN | c.1933T= (p.Phe645=) c.1741T= (p.Phe581=) c.1632T= n.772T= n.1507T= c.1891T= (p.Phe631=) c.1711T= (p.Phe571=) c.1699T= (p.Phe567=) c.1516T= (p.Phe506=) | |
| 1 | g.77942735T>A | CA340883223 | NEXN | c.1934T>A (p.Phe645Tyr) c.1742T>A (p.Phe581Tyr) c.1633T>A n.773T>A n.1508T>A c.1892T>A (p.Phe631Tyr) c.1712T>A (p.Phe571Tyr) c.1700T>A (p.Phe567Tyr) c.1517T>A (p.Phe506Tyr) | |
| 1 | g.77942735T>C | CA340883224 | NEXN | c.1934T>C (p.Phe645Ser) c.1742T>C (p.Phe581Ser) c.1633T>C n.773T>C n.1508T>C c.1892T>C (p.Phe631Ser) c.1712T>C (p.Phe571Ser) c.1700T>C (p.Phe567Ser) c.1517T>C (p.Phe506Ser) | |
| 1 | g.77942735T>G | CA340883225 | NEXN | c.1934T>G (p.Phe645Cys) c.1742T>G (p.Phe581Cys) c.1633T>G n.773T>G n.1508T>G c.1892T>G (p.Phe631Cys) c.1712T>G (p.Phe571Cys) c.1700T>G (p.Phe567Cys) c.1517T>G (p.Phe506Cys) | |
| 1 | g.77942736C>A | CA340883226 | NEXN | c.1935C>A (p.Phe645Leu) c.1743C>A (p.Phe581Leu) c.1634C>A n.774C>A n.1509C>A c.1893C>A (p.Phe631Leu) c.1713C>A (p.Phe571Leu) c.1701C>A (p.Phe567Leu) c.1518C>A (p.Phe506Leu) | |
| 1 | g.77942736C= | CA1177631457 | NEXN | c.1935C= (p.Phe645=) c.1743C= (p.Phe581=) c.1634C= n.774C= n.1509C= c.1893C= (p.Phe631=) c.1713C= (p.Phe571=) c.1701C= (p.Phe567=) c.1518C= (p.Phe506=) | |
| 1 | g.77942736C>G | CA335445 | NEXN | c.1935C>G (p.Phe645Leu) c.1743C>G (p.Phe581Leu) c.1634C>G n.774C>G n.1509C>G c.1893C>G (p.Phe631Leu) c.1713C>G (p.Phe571Leu) c.1701C>G (p.Phe567Leu) c.1518C>G (p.Phe506Leu) | ClinVar dbSNP gnomAD v4 |
| 1 | g.77942736C>T | CA418709792 | NEXN | c.1935C>T (p.Phe645=) c.1743C>T (p.Phe581=) c.1634C>T n.774C>T n.1509C>T c.1893C>T (p.Phe631=) c.1713C>T (p.Phe571=) c.1701C>T (p.Phe567=) c.1518C>T (p.Phe506=) | gnomAD v4 |
| 1 | g.77942737C>A | CA340883228 | NEXN | c.1936C>A (p.Pro646Thr) c.1744C>A (p.Pro582Thr) c.1635C>A n.775C>A n.1510C>A c.1894C>A (p.Pro632Thr) c.1714C>A (p.Pro572Thr) c.1702C>A (p.Pro568Thr) c.1519C>A (p.Pro507Thr) | |
| 1 | g.77942737C= | CA1177631458 | NEXN | c.1936C= (p.Pro646=) c.1744C= (p.Pro582=) c.1635C= n.775C= n.1510C= c.1894C= (p.Pro632=) c.1714C= (p.Pro572=) c.1702C= (p.Pro568=) c.1519C= (p.Pro507=) | |
| 1 | g.77942737C>G | CA919009 | NEXN | c.1936C>G (p.Pro646Ala) c.1744C>G (p.Pro582Ala) c.1635C>G n.775C>G n.1510C>G c.1894C>G (p.Pro632Ala) c.1714C>G (p.Pro572Ala) c.1702C>G (p.Pro568Ala) c.1519C>G (p.Pro507Ala) | dbSNP ExAC gnomAD v2 |
| 1 | g.77942737C>T | CA340883227 | NEXN | c.1936C>T (p.Pro646Ser) c.1744C>T (p.Pro582Ser) c.1635C>T n.775C>T n.1510C>T c.1894C>T (p.Pro632Ser) c.1714C>T (p.Pro572Ser) c.1702C>T (p.Pro568Ser) c.1519C>T (p.Pro507Ser) | |
| 1 | g.77942738C>A | CA142137 | NEXN | c.1937C>A (p.Pro646Gln) c.1745C>A (p.Pro582Gln) c.1636C>A n.776C>A n.1511C>A c.1895C>A (p.Pro632Gln) c.1715C>A (p.Pro572Gln) c.1703C>A (p.Pro568Gln) c.1520C>A (p.Pro507Gln) | ClinVar dbSNP |
| 1 | g.77942738C= | CA1144228879 | NEXN | c.1937C= (p.Pro646=) c.1745C= (p.Pro582=) c.1636C= n.776C= n.1511C= c.1895C= (p.Pro632=) c.1715C= (p.Pro572=) c.1703C= (p.Pro568=) c.1520C= (p.Pro507=) | |
| 1 | g.77942738C>G | CA340883229 | NEXN | c.1937C>G (p.Pro646Arg) c.1745C>G (p.Pro582Arg) c.1636C>G n.776C>G n.1511C>G c.1895C>G (p.Pro632Arg) c.1715C>G (p.Pro572Arg) c.1703C>G (p.Pro568Arg) c.1520C>G (p.Pro507Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77942738C>T | CA340883230 | NEXN | c.1937C>T (p.Pro646Leu) c.1745C>T (p.Pro582Leu) c.1636C>T n.776C>T n.1511C>T c.1895C>T (p.Pro632Leu) c.1715C>T (p.Pro572Leu) c.1703C>T (p.Pro568Leu) c.1520C>T (p.Pro507Leu) | |
| 1 | g.77942739A= | CA1177631459 | NEXN | c.1938A= (p.Pro646=) c.1746A= (p.Pro582=) c.1637A= n.777A= n.1512A= c.1896A= (p.Pro632=) c.1716A= (p.Pro572=) c.1704A= (p.Pro568=) c.1521A= (p.Pro507=) | |
| 1 | g.77942739A>C | CA418709794 | NEXN | c.1938A>C (p.Pro646=) c.1746A>C (p.Pro582=) c.1637A>C n.777A>C n.1512A>C c.1896A>C (p.Pro632=) c.1716A>C (p.Pro572=) c.1704A>C (p.Pro568=) c.1521A>C (p.Pro507=) | ClinVar dbSNP gnomAD v4 |
| 1 | g.77942739A>G | CA418709796 | NEXN | c.1938A>G (p.Pro646=) c.1746A>G (p.Pro582=) c.1637A>G n.777A>G n.1512A>G c.1896A>G (p.Pro632=) c.1716A>G (p.Pro572=) c.1704A>G (p.Pro568=) c.1521A>G (p.Pro507=) | |
| 1 | g.77942739A>T | CA418709797 | NEXN | c.1938A>T (p.Pro646=) c.1746A>T (p.Pro582=) c.1637A>T n.777A>T n.1512A>T c.1896A>T (p.Pro632=) c.1716A>T (p.Pro572=) c.1704A>T (p.Pro568=) c.1521A>T (p.Pro507=) | |
| 1 | g.77942740G>A | CA340883231 | NEXN | c.1939G>A (p.Glu647Lys) c.1747G>A (p.Glu583Lys) c.1638G>A n.778G>A n.1513G>A c.1897G>A (p.Glu633Lys) c.1717G>A (p.Glu573Lys) c.1705G>A (p.Glu569Lys) c.1522G>A (p.Glu508Lys) | |
| 1 | g.77942740G>C | CA340883232 | NEXN | c.1939G>C (p.Glu647Gln) c.1747G>C (p.Glu583Gln) c.1638G>C n.778G>C n.1513G>C c.1897G>C (p.Glu633Gln) c.1717G>C (p.Glu573Gln) c.1705G>C (p.Glu569Gln) c.1522G>C (p.Glu508Gln) | |
| 1 | g.77942740G>T | CA340883233 | NEXN | c.1939G>T (p.Glu647Ter) c.1747G>T (p.Glu583Ter) c.1638G>T n.778G>T n.1513G>T c.1897G>T (p.Glu633Ter) c.1717G>T (p.Glu573Ter) c.1705G>T (p.Glu569Ter) c.1522G>T (p.Glu508Ter) | |
| 1 | g.77942741A>C | CA340883236 | NEXN | c.1940A>C (p.Glu647Ala) c.1748A>C (p.Glu583Ala) c.1639A>C n.779A>C n.1514A>C c.1898A>C (p.Glu633Ala) c.1718A>C (p.Glu573Ala) c.1706A>C (p.Glu569Ala) c.1523A>C (p.Glu508Ala) | |
| 1 | g.77942741A>G | CA340883234 | NEXN | c.1940A>G (p.Glu647Gly) c.1748A>G (p.Glu583Gly) c.1639A>G n.779A>G n.1514A>G c.1898A>G (p.Glu633Gly) c.1718A>G (p.Glu573Gly) c.1706A>G (p.Glu569Gly) c.1523A>G (p.Glu508Gly) | |
| 1 | g.77942741A>T | CA340883235 | NEXN | c.1940A>T (p.Glu647Val) c.1748A>T (p.Glu583Val) c.1639A>T n.779A>T n.1514A>T c.1898A>T (p.Glu633Val) c.1718A>T (p.Glu573Val) c.1706A>T (p.Glu569Val) c.1523A>T (p.Glu508Val) | |
| 1 | g.77942742A>C | CA340883237 | NEXN | c.1941A>C (p.Glu647Asp) c.1749A>C (p.Glu583Asp) c.1640A>C n.780A>C n.1515A>C c.1899A>C (p.Glu633Asp) c.1719A>C (p.Glu573Asp) c.1707A>C (p.Glu569Asp) c.1524A>C (p.Glu508Asp) | |
| 1 | g.77942742A>G | CA418709801 | NEXN | c.1941A>G (p.Glu647=) c.1749A>G (p.Glu583=) c.1640A>G n.780A>G n.1515A>G c.1899A>G (p.Glu633=) c.1719A>G (p.Glu573=) c.1707A>G (p.Glu569=) c.1524A>G (p.Glu508=) | |
| 1 | g.77942742A>T | CA340883238 | NEXN | c.1941A>T (p.Glu647Asp) c.1749A>T (p.Glu583Asp) c.1640A>T n.780A>T n.1515A>T c.1899A>T (p.Glu633Asp) c.1719A>T (p.Glu573Asp) c.1707A>T (p.Glu569Asp) c.1524A>T (p.Glu508Asp) | |
| 1 | g.77942743G>A | CA340883239 | NEXN | c.1942G>A (p.Asp648Asn) c.1750G>A (p.Asp584Asn) c.1641G>A n.781G>A n.1516G>A c.1900G>A (p.Asp634Asn) c.1720G>A (p.Asp574Asn) c.1708G>A (p.Asp570Asn) c.1525G>A (p.Asp509Asn) | gnomAD v4 |
| 1 | g.77942743G>C | CA340883240 | NEXN | c.1942G>C (p.Asp648His) c.1750G>C (p.Asp584His) c.1641G>C n.781G>C n.1516G>C c.1900G>C (p.Asp634His) c.1720G>C (p.Asp574His) c.1708G>C (p.Asp570His) c.1525G>C (p.Asp509His) | |
| 1 | g.77942743G>T | CA340883241 | NEXN | c.1942G>T (p.Asp648Tyr) c.1750G>T (p.Asp584Tyr) c.1641G>T n.781G>T n.1516G>T c.1900G>T (p.Asp634Tyr) c.1720G>T (p.Asp574Tyr) c.1708G>T (p.Asp570Tyr) c.1525G>T (p.Asp509Tyr) | |
| 1 | g.77942744A= | CA1177631460 | NEXN | c.1943A= (p.Asp648=) c.1751A= (p.Asp584=) c.1642A= n.782A= n.1517A= c.1901A= (p.Asp634=) c.1721A= (p.Asp574=) c.1709A= (p.Asp570=) c.1526A= (p.Asp509=) | |
| 1 | g.77942744A>C | CA340883243 | NEXN | c.1943A>C (p.Asp648Ala) c.1751A>C (p.Asp584Ala) c.1642A>C n.782A>C n.1517A>C c.1901A>C (p.Asp634Ala) c.1721A>C (p.Asp574Ala) c.1709A>C (p.Asp570Ala) c.1526A>C (p.Asp509Ala) | |
| 1 | g.77942744A>G | CA919010 | NEXN | c.1943A>G (p.Asp648Gly) c.1751A>G (p.Asp584Gly) c.1642A>G n.782A>G n.1517A>G c.1901A>G (p.Asp634Gly) c.1721A>G (p.Asp574Gly) c.1709A>G (p.Asp570Gly) c.1526A>G (p.Asp509Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.77942744A>T | CA340883242 | NEXN | c.1943A>T (p.Asp648Val) c.1751A>T (p.Asp584Val) c.1642A>T n.782A>T n.1517A>T c.1901A>T (p.Asp634Val) c.1721A>T (p.Asp574Val) c.1709A>T (p.Asp570Val) c.1526A>T (p.Asp509Val) | dbSNP gnomAD v2 |
| 1 | g.77942745T>A | CA340883244 | NEXN | c.1944T>A (p.Asp648Glu) c.1752T>A (p.Asp584Glu) c.1643T>A n.783T>A n.1518T>A c.1902T>A (p.Asp634Glu) c.1722T>A (p.Asp574Glu) c.1710T>A (p.Asp570Glu) c.1527T>A (p.Asp509Glu) | |
| 1 | g.77942745T>C | CA418709807 | NEXN | c.1944T>C (p.Asp648=) c.1752T>C (p.Asp584=) c.1643T>C n.783T>C n.1518T>C c.1902T>C (p.Asp634=) c.1722T>C (p.Asp574=) c.1710T>C (p.Asp570=) c.1527T>C (p.Asp509=) | gnomAD v4 |
| 1 | g.77942745T>G | CA340883245 | NEXN | c.1944T>G (p.Asp648Glu) c.1752T>G (p.Asp584Glu) c.1643T>G n.783T>G n.1518T>G c.1902T>G (p.Asp634Glu) c.1722T>G (p.Asp574Glu) c.1710T>G (p.Asp570Glu) c.1527T>G (p.Asp509Glu) | |
| 1 | g.77942745_77942748delinsTGGA | CA1177631461 | NEXN | c.1944_1947delinsTGGA (p.Asp648=) c.1752_1755delinsTGGA (p.Asp584=) c.1643_1646delinsTGGA n.783_786delinsTGGA n.1518_1521delinsTGGA c.1902_1905delinsTGGA (p.Asp634=) c.1722_1725delinsTGGA (p.Asp574=) c.1710_1713delinsTGGA (p.Asp570=) c.1527_1530delinsTGGA (p.Asp509=) | |
| 1 | g.77942746G>A | CA340883246 | NEXN | c.1945G>A (p.Gly649Arg) c.1753G>A (p.Gly585Arg) c.1644G>A n.784G>A n.1519G>A c.1903G>A (p.Gly635Arg) c.1723G>A (p.Gly575Arg) c.1711G>A (p.Gly571Arg) c.1528G>A (p.Gly510Arg) | |
| 1 | g.77942746G>C | CA340883247 | NEXN | c.1945G>C (p.Gly649Arg) c.1753G>C (p.Gly585Arg) c.1644G>C n.784G>C n.1519G>C c.1903G>C (p.Gly635Arg) c.1723G>C (p.Gly575Arg) c.1711G>C (p.Gly571Arg) c.1528G>C (p.Gly510Arg) | |
| 1 | g.77942746G>T | CA340883248 | NEXN | c.1945G>T (p.Gly649Ter) c.1753G>T (p.Gly585Ter) c.1644G>T n.784G>T n.1519G>T c.1903G>T (p.Gly635Ter) c.1723G>T (p.Gly575Ter) c.1711G>T (p.Gly571Ter) c.1528G>T (p.Gly510Ter) | |
| 1 | g.77942746_77942752delinsGGAGGAG | CA1144228880 | NEXN | c.1945_1951delinsGGAGGAG (p.Gly649=) c.1753_1759delinsGGAGGAG (p.Gly585=) c.1644_1650delinsGGAGGAG n.784_790delinsGGAGGAG n.1519_1525delinsGGAGGAG c.1903_1909delinsGGAGGAG (p.Gly635=) c.1723_1729delinsGGAGGAG (p.Gly575=) c.1711_1717delinsGGAGGAG (p.Gly571=) c.1528_1534delinsGGAGGAG (p.Gly510=) | |
| 1 | g.77942750_77942752del | CA142140 | NEXN | c.1949_1951del (p.Gly650del) c.1757_1759del (p.Gly586del) c.1648_1650del n.788_790del n.1523_1525del c.1907_1909del (p.Gly636del) c.1727_1729del (p.Gly576del) c.1715_1717del (p.Gly572del) c.1532_1534del (p.Gly511del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77942747G>A | CA340883249 | NEXN | c.1946G>A (p.Gly649Glu) c.1754G>A (p.Gly585Glu) c.1645G>A n.785G>A n.1520G>A c.1904G>A (p.Gly635Glu) c.1724G>A (p.Gly575Glu) c.1712G>A (p.Gly571Glu) c.1529G>A (p.Gly510Glu) | |
| 1 | g.77942747G>C | CA340883250 | NEXN | c.1946G>C (p.Gly649Ala) c.1754G>C (p.Gly585Ala) c.1645G>C n.785G>C n.1520G>C c.1904G>C (p.Gly635Ala) c.1724G>C (p.Gly575Ala) c.1712G>C (p.Gly571Ala) c.1529G>C (p.Gly510Ala) | |
| 1 | g.77942747G>T | CA340883251 | NEXN | c.1946G>T (p.Gly649Val) c.1754G>T (p.Gly585Val) c.1645G>T n.785G>T n.1520G>T c.1904G>T (p.Gly635Val) c.1724G>T (p.Gly575Val) c.1712G>T (p.Gly571Val) c.1529G>T (p.Gly510Val) | |
| 1 | g.77942748A>C | CA418709813 | NEXN | c.1947A>C (p.Gly649=) c.1755A>C (p.Gly585=) c.1646A>C n.786A>C n.1521A>C c.1905A>C (p.Gly635=) c.1725A>C (p.Gly575=) c.1713A>C (p.Gly571=) c.1530A>C (p.Gly510=) | |
| 1 | g.77942748A>G | CA418709811 | NEXN | c.1947A>G (p.Gly649=) c.1755A>G (p.Gly585=) c.1646A>G n.786A>G n.1521A>G c.1905A>G (p.Gly635=) c.1725A>G (p.Gly575=) c.1713A>G (p.Gly571=) c.1530A>G (p.Gly510=) | |
| 1 | g.77942748A>T | CA418709812 | NEXN | c.1947A>T (p.Gly649=) c.1755A>T (p.Gly585=) c.1646A>T n.786A>T n.1521A>T c.1905A>T (p.Gly635=) c.1725A>T (p.Gly575=) c.1713A>T (p.Gly571=) c.1530A>T (p.Gly510=) | |
| 1 | g.77942749G>A | CA340883252 | NEXN | c.1948G>A (p.Gly650Arg) c.1756G>A (p.Gly586Arg) c.1647G>A n.787G>A n.1522G>A c.1906G>A (p.Gly636Arg) c.1726G>A (p.Gly576Arg) c.1714G>A (p.Gly572Arg) c.1531G>A (p.Gly511Arg) | ClinVar gnomAD v4 |
| 1 | g.77942749G>C | CA340883253 | NEXN | c.1948G>C (p.Gly650Arg) c.1756G>C (p.Gly586Arg) c.1647G>C n.787G>C n.1522G>C c.1906G>C (p.Gly636Arg) c.1726G>C (p.Gly576Arg) c.1714G>C (p.Gly572Arg) c.1531G>C (p.Gly511Arg) | |
| 1 | g.77942749G>T | CA340883254 | NEXN | c.1948G>T (p.Gly650Ter) c.1756G>T (p.Gly586Ter) c.1647G>T n.787G>T n.1522G>T c.1906G>T (p.Gly636Ter) c.1726G>T (p.Gly576Ter) c.1714G>T (p.Gly572Ter) c.1531G>T (p.Gly511Ter) | |
| 1 | g.77942749_77942751delinsGGA | CA1177631462 | NEXN | c.1948_1950delinsGGA (p.Gly650=) c.1756_1758delinsGGA (p.Gly586=) c.1647_1649delinsGGA n.787_789delinsGGA n.1522_1524delinsGGA c.1906_1908delinsGGA (p.Gly636=) c.1726_1728delinsGGA (p.Gly576=) c.1714_1716delinsGGA (p.Gly572=) c.1531_1533delinsGGA (p.Gly511=) | |
| 1 | g.77942750G>A | CA340883257 | NEXN | c.1949G>A (p.Gly650Glu) c.1757G>A (p.Gly586Glu) c.1648G>A n.788G>A n.1523G>A c.1907G>A (p.Gly636Glu) c.1727G>A (p.Gly576Glu) c.1715G>A (p.Gly572Glu) c.1532G>A (p.Gly511Glu) | |
| 1 | g.77942750G>C | CA340883255 | NEXN | c.1949G>C (p.Gly650Ala) c.1757G>C (p.Gly586Ala) c.1648G>C n.788G>C n.1523G>C c.1907G>C (p.Gly636Ala) c.1727G>C (p.Gly576Ala) c.1715G>C (p.Gly572Ala) c.1532G>C (p.Gly511Ala) | |
| 1 | g.77942750G>T | CA340883256 | NEXN | c.1949G>T (p.Gly650Val) c.1757G>T (p.Gly586Val) c.1648G>T n.788G>T n.1523G>T c.1907G>T (p.Gly636Val) c.1727G>T (p.Gly576Val) c.1715G>T (p.Gly572Val) c.1532G>T (p.Gly511Val) | gnomAD v4 |
| 1 | g.77942753_77942754del | CA658795481 | NEXN | c.1952_1953del (p.Glu651ValfsTer4) c.1760_1761del (p.Glu587ValfsTer4) c.1651_1652del n.1526_1527del c.1910_1911del (p.Glu637ValfsTer4) c.1730_1731del (p.Glu577ValfsTer4) c.1718_1719del (p.Glu573ValfsTer4) c.1535_1536del (p.Glu512ValfsTer4) | ClinVar dbSNP gnomAD v4 |
| 1 | g.77942751A>C | CA418709815 | NEXN | c.1950A>C (p.Gly650=) c.1758A>C (p.Gly586=) c.1649A>C n.789A>C n.1524A>C c.1908A>C (p.Gly636=) c.1728A>C (p.Gly576=) c.1716A>C (p.Gly572=) c.1533A>C (p.Gly511=) | gnomAD v4 |
| 1 | g.77942751A>G | CA418709817 | NEXN | c.1950A>G (p.Gly650=) c.1758A>G (p.Gly586=) c.1649A>G n.789A>G n.1524A>G c.1908A>G (p.Gly636=) c.1728A>G (p.Gly576=) c.1716A>G (p.Gly572=) c.1533A>G (p.Gly511=) | ClinVar dbSNP |
| 1 | g.77942751A>T | CA418709818 | NEXN | c.1950A>T (p.Gly650=) c.1758A>T (p.Gly586=) c.1649A>T n.789A>T n.1524A>T c.1908A>T (p.Gly636=) c.1728A>T (p.Gly576=) c.1716A>T (p.Gly572=) c.1533A>T (p.Gly511=) | |
| 1 | g.77942752G>A | CA340883260 | NEXN | c.1951G>A (p.Glu651Lys) c.1759G>A (p.Glu587Lys) c.1650G>A n.790G>A n.1525G>A c.1909G>A (p.Glu637Lys) c.1729G>A (p.Glu577Lys) c.1717G>A (p.Glu573Lys) c.1534G>A (p.Glu512Lys) | ClinVar dbSNP gnomAD v4 |
| 1 | g.77942752G>C | CA340883258 | NEXN | c.1951G>C (p.Glu651Gln) c.1759G>C (p.Glu587Gln) c.1650G>C n.790G>C n.1525G>C c.1909G>C (p.Glu637Gln) c.1729G>C (p.Glu577Gln) c.1717G>C (p.Glu573Gln) c.1534G>C (p.Glu512Gln) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 1 | g.77942752G= | CA1177631463 | NEXN | c.1951G= (p.Glu651=) c.1759G= (p.Glu587=) c.1650G= n.790G= n.1525G= c.1909G= (p.Glu637=) c.1729G= (p.Glu577=) c.1717G= (p.Glu573=) c.1534G= (p.Glu512=) | |
| 1 | g.77942752G>T | CA340883259 | NEXN | c.1951G>T (p.Glu651Ter) c.1759G>T (p.Glu587Ter) c.1650G>T n.790G>T n.1525G>T c.1909G>T (p.Glu637Ter) c.1729G>T (p.Glu577Ter) c.1717G>T (p.Glu573Ter) c.1534G>T (p.Glu512Ter) | |
| 1 | g.77942753A>C | CA340883261 | NEXN | c.1952A>C (p.Glu651Ala) c.1760A>C (p.Glu587Ala) c.1651A>C n.791A>C n.1526A>C c.1910A>C (p.Glu637Ala) c.1730A>C (p.Glu577Ala) c.1718A>C (p.Glu573Ala) c.1535A>C (p.Glu512Ala) | |
| 1 | g.77942753A>G | CA340883262 | NEXN | c.1952A>G (p.Glu651Gly) c.1760A>G (p.Glu587Gly) c.1651A>G n.791A>G n.1526A>G c.1910A>G (p.Glu637Gly) c.1730A>G (p.Glu577Gly) c.1718A>G (p.Glu573Gly) c.1535A>G (p.Glu512Gly) | |
| 1 | g.77942753A>T | CA340883263 | NEXN | c.1952A>T (p.Glu651Val) c.1760A>T (p.Glu587Val) c.1651A>T n.791A>T n.1526A>T c.1910A>T (p.Glu637Val) c.1730A>T (p.Glu577Val) c.1718A>T (p.Glu573Val) c.1535A>T (p.Glu512Val) | |
| 1 | g.77942754G>A | CA418709819 | NEXN | c.1953G>A (p.Glu651=) c.1761G>A (p.Glu587=) c.1652G>A n.1527G>A c.1911G>A (p.Glu637=) c.1731G>A (p.Glu577=) c.1719G>A (p.Glu573=) c.1536G>A (p.Glu512=) | |
| 1 | g.77942754G>C | CA340883264 | NEXN | c.1953G>C (p.Glu651Asp) c.1761G>C (p.Glu587Asp) c.1652G>C n.1527G>C c.1911G>C (p.Glu637Asp) c.1731G>C (p.Glu577Asp) c.1719G>C (p.Glu573Asp) c.1536G>C (p.Glu512Asp) | |
| 1 | g.77942754G>T | CA340883265 | NEXN | c.1953G>T (p.Glu651Asp) c.1761G>T (p.Glu587Asp) c.1652G>T n.1527G>T c.1911G>T (p.Glu637Asp) c.1731G>T (p.Glu577Asp) c.1719G>T (p.Glu573Asp) c.1536G>T (p.Glu512Asp) | |
| 1 | g.77942755T>A | CA340883266 | NEXN | c.1954T>A (p.Tyr652Asn) c.1762T>A (p.Tyr588Asn) c.1653T>A n.1528T>A c.1912T>A (p.Tyr638Asn) c.1732T>A (p.Tyr578Asn) c.1720T>A (p.Tyr574Asn) c.1537T>A (p.Tyr513Asn) | gnomAD v4 |
| 1 | g.77942755T>C | CA340883267 | NEXN | c.1954T>C (p.Tyr652His) c.1762T>C (p.Tyr588His) c.1653T>C n.1528T>C c.1912T>C (p.Tyr638His) c.1732T>C (p.Tyr578His) c.1720T>C (p.Tyr574His) c.1537T>C (p.Tyr513His) | |
| 1 | g.77942755T>G | CA340883268 | NEXN | c.1954T>G (p.Tyr652Asp) c.1762T>G (p.Tyr588Asp) c.1653T>G n.1528T>G c.1912T>G (p.Tyr638Asp) c.1732T>G (p.Tyr578Asp) c.1720T>G (p.Tyr574Asp) c.1537T>G (p.Tyr513Asp) | |
| 1 | g.77942758_77942759del | CA2740152414 | NEXN | c.1957_1958del (p.Met653ValfsTer2) c.1765_1766del (p.Met589ValfsTer2) c.1656_1657del n.1531_1532del c.1915_1916del (p.Met639ValfsTer2) c.1735_1736del (p.Met579ValfsTer2) c.1723_1724del (p.Met575ValfsTer2) c.1540_1541del (p.Met514ValfsTer2) | |
| 1 | g.77942756A= | CA1141580867 | NEXN | c.1955A= (p.Tyr652=) c.1763A= (p.Tyr588=) c.1654A= n.1529A= c.1913A= (p.Tyr638=) c.1733A= (p.Tyr578=) c.1721A= (p.Tyr574=) c.1538A= (p.Tyr513=) | |
| 1 | g.77942756A>C | CA340883269 | NEXN | c.1955A>C (p.Tyr652Ser) c.1763A>C (p.Tyr588Ser) c.1654A>C n.1529A>C c.1913A>C (p.Tyr638Ser) c.1733A>C (p.Tyr578Ser) c.1721A>C (p.Tyr574Ser) c.1538A>C (p.Tyr513Ser) | |
| 1 | g.77942756A>G | CA142143 | NEXN | c.1955A>G (p.Tyr652Cys) c.1763A>G (p.Tyr588Cys) c.1654A>G n.1529A>G c.1913A>G (p.Tyr638Cys) c.1733A>G (p.Tyr578Cys) c.1721A>G (p.Tyr574Cys) c.1538A>G (p.Tyr513Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77942756A>T | CA340883270 | NEXN | c.1955A>T (p.Tyr652Phe) c.1763A>T (p.Tyr588Phe) c.1654A>T n.1529A>T c.1913A>T (p.Tyr638Phe) c.1733A>T (p.Tyr578Phe) c.1721A>T (p.Tyr574Phe) c.1538A>T (p.Tyr513Phe) | |
| 1 | g.77942757T>A | CA340883271 | NEXN | c.1956T>A (p.Tyr652Ter) c.1764T>A (p.Tyr588Ter) c.1655T>A n.1530T>A c.1914T>A (p.Tyr638Ter) c.1734T>A (p.Tyr578Ter) c.1722T>A (p.Tyr574Ter) c.1539T>A (p.Tyr513Ter) | |
| 1 | g.77942757T>C | CA418709824 | NEXN | c.1956T>C (p.Tyr652=) c.1764T>C (p.Tyr588=) c.1655T>C n.1530T>C c.1914T>C (p.Tyr638=) c.1734T>C (p.Tyr578=) c.1722T>C (p.Tyr574=) c.1539T>C (p.Tyr513=) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77942757T>G | CA340883272 | NEXN | c.1956T>G (p.Tyr652Ter) c.1764T>G (p.Tyr588Ter) c.1655T>G n.1530T>G c.1914T>G (p.Tyr638Ter) c.1734T>G (p.Tyr578Ter) c.1722T>G (p.Tyr574Ter) c.1539T>G (p.Tyr513Ter) | |
| 1 | g.77942757T= | CA1177631464 | NEXN | c.1956T= (p.Tyr652=) c.1764T= (p.Tyr588=) c.1655T= n.1530T= c.1914T= (p.Tyr638=) c.1734T= (p.Tyr578=) c.1722T= (p.Tyr574=) c.1539T= (p.Tyr513=) | |
| 1 | g.77942758A= | CA1177631465 | NEXN | c.1957A= (p.Met653=) c.1765A= (p.Met589=) c.1656A= n.1531A= c.1915A= (p.Met639=) c.1735A= (p.Met579=) c.1723A= (p.Met575=) c.1540A= (p.Met514=) | |
| 1 | g.77942758A>C | CA340883273 | NEXN | c.1957A>C (p.Met653Leu) c.1765A>C (p.Met589Leu) c.1656A>C n.1531A>C c.1915A>C (p.Met639Leu) c.1735A>C (p.Met579Leu) c.1723A>C (p.Met575Leu) c.1540A>C (p.Met514Leu) | |
| 1 | g.77942758A>G | CA919011 | NEXN | c.1957A>G (p.Met653Val) c.1765A>G (p.Met589Val) c.1656A>G n.1531A>G c.1915A>G (p.Met639Val) c.1735A>G (p.Met579Val) c.1723A>G (p.Met575Val) c.1540A>G (p.Met514Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77942758A>T | CA340883274 | NEXN | c.1957A>T (p.Met653Leu) c.1765A>T (p.Met589Leu) c.1656A>T n.1531A>T c.1915A>T (p.Met639Leu) c.1735A>T (p.Met579Leu) c.1723A>T (p.Met575Leu) c.1540A>T (p.Met514Leu) | |
| 1 | g.77942759T>A | CA340883275 | NEXN | c.1958T>A (p.Met653Lys) c.1766T>A (p.Met589Lys) c.1657T>A n.1532T>A c.1916T>A (p.Met639Lys) c.1736T>A (p.Met579Lys) c.1724T>A (p.Met575Lys) c.1541T>A (p.Met514Lys) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.77942759T>C | CA919012 | NEXN | c.1958T>C (p.Met653Thr) c.1766T>C (p.Met589Thr) c.1657T>C n.1532T>C c.1916T>C (p.Met639Thr) c.1736T>C (p.Met579Thr) c.1724T>C (p.Met575Thr) c.1541T>C (p.Met514Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77942759T>G | CA340883276 | NEXN | c.1958T>G (p.Met653Arg) c.1766T>G (p.Met589Arg) c.1657T>G n.1532T>G c.1916T>G (p.Met639Arg) c.1736T>G (p.Met579Arg) c.1724T>G (p.Met575Arg) c.1541T>G (p.Met514Arg) | |
| 1 | g.77942759T= | CA1177631466 | NEXN | c.1958T= (p.Met653=) c.1766T= (p.Met589=) c.1657T= n.1532T= c.1916T= (p.Met639=) c.1736T= (p.Met579=) c.1724T= (p.Met575=) c.1541T= (p.Met514=) | |
| 1 | g.77942760G>A | CA340883277 | NEXN | c.1959G>A (p.Met653Ile) c.1767G>A (p.Met589Ile) c.1658G>A n.1533G>A c.1917G>A (p.Met639Ile) c.1737G>A (p.Met579Ile) c.1725G>A (p.Met575Ile) c.1542G>A (p.Met514Ile) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.77942760G>C | CA340883278 | NEXN | c.1959G>C (p.Met653Ile) c.1767G>C (p.Met589Ile) c.1658G>C n.1533G>C c.1917G>C (p.Met639Ile) c.1737G>C (p.Met579Ile) c.1725G>C (p.Met575Ile) c.1542G>C (p.Met514Ile) | |
| 1 | g.77942760G= | CA1177631467 | NEXN | c.1959G= (p.Met653=) c.1767G= (p.Met589=) c.1658G= n.1533G= c.1917G= (p.Met639=) c.1737G= (p.Met579=) c.1725G= (p.Met575=) c.1542G= (p.Met514=) | |
| 1 | g.77942760G>T | CA340883279 | NEXN | c.1959G>T (p.Met653Ile) c.1767G>T (p.Met589Ile) c.1658G>T n.1533G>T c.1917G>T (p.Met639Ile) c.1737G>T (p.Met579Ile) c.1725G>T (p.Met575Ile) c.1542G>T (p.Met514Ile) | |
| 1 | g.77942761T>A | CA340883281 | NEXN | c.1960T>A (p.Cys654Ser) c.1768T>A (p.Cys590Ser) c.1659T>A n.1534T>A c.1918T>A (p.Cys640Ser) c.1738T>A (p.Cys580Ser) c.1726T>A (p.Cys576Ser) c.1543T>A (p.Cys515Ser) | |
| 1 | g.77942761T>C | CA340883282 | NEXN | c.1960T>C (p.Cys654Arg) c.1768T>C (p.Cys590Arg) c.1659T>C n.1534T>C c.1918T>C (p.Cys640Arg) c.1738T>C (p.Cys580Arg) c.1726T>C (p.Cys576Arg) c.1543T>C (p.Cys515Arg) | |
| 1 | g.77942761T>G | CA340883283 | NEXN | c.1960T>G (p.Cys654Gly) c.1768T>G (p.Cys590Gly) c.1659T>G n.1534T>G c.1918T>G (p.Cys640Gly) c.1738T>G (p.Cys580Gly) c.1726T>G (p.Cys576Gly) c.1543T>G (p.Cys515Gly) | |
| 1 | g.77942762G>A | CA340883285 | NEXN | c.1961G>A (p.Cys654Tyr) c.1769G>A (p.Cys590Tyr) c.1660G>A n.1535G>A c.1919G>A (p.Cys640Tyr) c.1739G>A (p.Cys580Tyr) c.1727G>A (p.Cys576Tyr) c.1544G>A (p.Cys515Tyr) | |
| 1 | g.77942762G>C | CA340883286 | NEXN | c.1961G>C (p.Cys654Ser) c.1769G>C (p.Cys590Ser) c.1660G>C n.1535G>C c.1919G>C (p.Cys640Ser) c.1739G>C (p.Cys580Ser) c.1727G>C (p.Cys576Ser) c.1544G>C (p.Cys515Ser) | |
| 1 | g.77942762G>T | CA340883284 | NEXN | c.1961G>T (p.Cys654Phe) c.1769G>T (p.Cys590Phe) c.1660G>T n.1535G>T c.1919G>T (p.Cys640Phe) c.1739G>T (p.Cys580Phe) c.1727G>T (p.Cys576Phe) c.1544G>T (p.Cys515Phe) | |
| 1 | g.77942763T>A | CA340883287 | NEXN | c.1962T>A (p.Cys654Ter) c.1770T>A (p.Cys590Ter) c.1661T>A n.1536T>A c.1920T>A (p.Cys640Ter) c.1740T>A (p.Cys580Ter) c.1728T>A (p.Cys576Ter) c.1545T>A (p.Cys515Ter) | |
| 1 | g.77942763T>C | CA24692011 | NEXN | c.1962T>C (p.Cys654=) c.1770T>C (p.Cys590=) c.1661T>C n.1536T>C c.1920T>C (p.Cys640=) c.1740T>C (p.Cys580=) c.1728T>C (p.Cys576=) c.1545T>C (p.Cys515=) | dbSNP gnomAD v4 |
| 1 | g.77942763T>G | CA340883288 | NEXN | c.1962T>G (p.Cys654Trp) c.1770T>G (p.Cys590Trp) c.1661T>G n.1536T>G c.1920T>G (p.Cys640Trp) c.1740T>G (p.Cys580Trp) c.1728T>G (p.Cys576Trp) c.1545T>G (p.Cys515Trp) | |
| 1 | g.77942763T= | CA1177631468 | NEXN | c.1962T= (p.Cys654=) c.1770T= (p.Cys590=) c.1661T= n.1536T= c.1920T= (p.Cys640=) c.1740T= (p.Cys580=) c.1728T= (p.Cys576=) c.1545T= (p.Cys515=) | |
| 1 | g.77942764A>C | CA340883289 | NEXN | c.1963A>C (p.Lys655Gln) c.1771A>C (p.Lys591Gln) c.1662A>C n.1537A>C c.1921A>C (p.Lys641Gln) c.1741A>C (p.Lys581Gln) c.1729A>C (p.Lys577Gln) c.1546A>C (p.Lys516Gln) | |
| 1 | g.77942764A>G | CA340883290 | NEXN | c.1963A>G (p.Lys655Glu) c.1771A>G (p.Lys591Glu) c.1662A>G n.1537A>G c.1921A>G (p.Lys641Glu) c.1741A>G (p.Lys581Glu) c.1729A>G (p.Lys577Glu) c.1546A>G (p.Lys516Glu) | gnomAD v4 |
| 1 | g.77942764A>T | CA340883291 | NEXN | c.1963A>T (p.Lys655Ter) c.1771A>T (p.Lys591Ter) c.1662A>T n.1537A>T c.1921A>T (p.Lys641Ter) c.1741A>T (p.Lys581Ter) c.1729A>T (p.Lys577Ter) c.1546A>T (p.Lys516Ter) | |
| 1 | g.77942765A>C | CA340883292 | NEXN | c.1964A>C (p.Lys655Thr) c.1772A>C (p.Lys591Thr) c.1663A>C n.1538A>C c.1922A>C (p.Lys641Thr) c.1742A>C (p.Lys581Thr) c.1730A>C (p.Lys577Thr) c.1547A>C (p.Lys516Thr) | |
| 1 | g.77942765A>G | CA340883293 | NEXN | c.1964A>G (p.Lys655Arg) c.1772A>G (p.Lys591Arg) c.1663A>G n.1538A>G c.1922A>G (p.Lys641Arg) c.1742A>G (p.Lys581Arg) c.1730A>G (p.Lys577Arg) c.1547A>G (p.Lys516Arg) | |
| 1 | g.77942765A>T | CA340883294 | NEXN | c.1964A>T (p.Lys655Ile) c.1772A>T (p.Lys591Ile) c.1663A>T n.1538A>T c.1922A>T (p.Lys641Ile) c.1742A>T (p.Lys581Ile) c.1730A>T (p.Lys577Ile) c.1547A>T (p.Lys516Ile) | |
| 1 | g.77942766A= | CA1177631469 | NEXN | c.1965A= (p.Lys655=) c.1773A= (p.Lys591=) c.1664A= n.1539A= c.1923A= (p.Lys641=) c.1743A= (p.Lys581=) c.1731A= (p.Lys577=) c.1548A= (p.Lys516=) | |
| 1 | g.77942766A>C | CA340883295 | NEXN | c.1965A>C (p.Lys655Asn) c.1773A>C (p.Lys591Asn) c.1664A>C n.1539A>C c.1923A>C (p.Lys641Asn) c.1743A>C (p.Lys581Asn) c.1731A>C (p.Lys577Asn) c.1548A>C (p.Lys516Asn) | |
| 1 | g.77942766A>G | CA919013 | NEXN | c.1965A>G (p.Lys655=) c.1773A>G (p.Lys591=) c.1664A>G n.1539A>G c.1923A>G (p.Lys641=) c.1743A>G (p.Lys581=) c.1731A>G (p.Lys577=) c.1548A>G (p.Lys516=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77942766A>T | CA340883296 | NEXN | c.1965A>T (p.Lys655Asn) c.1773A>T (p.Lys591Asn) c.1664A>T n.1539A>T c.1923A>T (p.Lys641Asn) c.1743A>T (p.Lys581Asn) c.1731A>T (p.Lys577Asn) c.1548A>T (p.Lys516Asn) | dbSNP |
| 1 | g.77942767G>A | CA340883297 | NEXN | c.1966G>A (p.Ala656Thr) c.1774G>A (p.Ala592Thr) c.1665G>A n.1540G>A c.1924G>A (p.Ala642Thr) c.1744G>A (p.Ala582Thr) c.1732G>A (p.Ala578Thr) c.1549G>A (p.Ala517Thr) | |
| 1 | g.77942767G>C | CA340883298 | NEXN | c.1966G>C (p.Ala656Pro) c.1774G>C (p.Ala592Pro) c.1665G>C n.1540G>C c.1924G>C (p.Ala642Pro) c.1744G>C (p.Ala582Pro) c.1732G>C (p.Ala578Pro) c.1549G>C (p.Ala517Pro) | |
| 1 | g.77942767G>T | CA340883299 | NEXN | c.1966G>T (p.Ala656Ser) c.1774G>T (p.Ala592Ser) c.1665G>T n.1540G>T c.1924G>T (p.Ala642Ser) c.1744G>T (p.Ala582Ser) c.1732G>T (p.Ala578Ser) c.1549G>T (p.Ala517Ser) | |
| 1 | g.77942768C>A | CA340883302 | NEXN | c.1967C>A (p.Ala656Glu) c.1775C>A (p.Ala592Glu) c.1666C>A n.1541C>A c.1925C>A (p.Ala642Glu) c.1745C>A (p.Ala582Glu) c.1733C>A (p.Ala578Glu) c.1550C>A (p.Ala517Glu) | gnomAD v4 |
| 1 | g.77942768C>G | CA340883300 | NEXN | c.1967C>G (p.Ala656Gly) c.1775C>G (p.Ala592Gly) c.1666C>G n.1541C>G c.1925C>G (p.Ala642Gly) c.1745C>G (p.Ala582Gly) c.1733C>G (p.Ala578Gly) c.1550C>G (p.Ala517Gly) | |
| 1 | g.77942768C>T | CA340883301 | NEXN | c.1967C>T (p.Ala656Val) c.1775C>T (p.Ala592Val) c.1666C>T n.1541C>T c.1925C>T (p.Ala642Val) c.1745C>T (p.Ala582Val) c.1733C>T (p.Ala578Val) c.1550C>T (p.Ala517Val) | |
| 1 | g.77942769A>C | CA418709835 | NEXN | c.1968A>C (p.Ala656=) c.1776A>C (p.Ala592=) c.1667A>C n.1542A>C c.1926A>C (p.Ala642=) c.1746A>C (p.Ala582=) c.1734A>C (p.Ala578=) c.1551A>C (p.Ala517=) | |
| 1 | g.77942769A>G | CA418709836 | NEXN | c.1968A>G (p.Ala656=) c.1776A>G (p.Ala592=) c.1667A>G n.1542A>G c.1926A>G (p.Ala642=) c.1746A>G (p.Ala582=) c.1734A>G (p.Ala578=) c.1551A>G (p.Ala517=) | |
| 1 | g.77942769A>T | CA418709837 | NEXN | c.1968A>T (p.Ala656=) c.1776A>T (p.Ala592=) c.1667A>T n.1542A>T c.1926A>T (p.Ala642=) c.1746A>T (p.Ala582=) c.1734A>T (p.Ala578=) c.1551A>T (p.Ala517=) | gnomAD v4 |
| 1 | g.77942770G>A | CA340883303 | NEXN | c.1969G>A (p.Val657Ile) c.1777G>A (p.Val593Ile) c.1668G>A n.1543G>A c.1927G>A (p.Val643Ile) c.1747G>A (p.Val583Ile) c.1735G>A (p.Val579Ile) c.1552G>A (p.Val518Ile) | |
| 1 | g.77942770G>C | CA340883304 | NEXN | c.1969G>C (p.Val657Leu) c.1777G>C (p.Val593Leu) c.1668G>C n.1543G>C c.1927G>C (p.Val643Leu) c.1747G>C (p.Val583Leu) c.1735G>C (p.Val579Leu) c.1552G>C (p.Val518Leu) | gnomAD v4 |
| 1 | g.77942770G>T | CA340883305 | NEXN | c.1969G>T (p.Val657Phe) c.1777G>T (p.Val593Phe) c.1668G>T n.1543G>T c.1927G>T (p.Val643Phe) c.1747G>T (p.Val583Phe) c.1735G>T (p.Val579Phe) c.1552G>T (p.Val518Phe) | |
| 1 | g.77942771T>A | CA340883306 | NEXN | c.1970T>A (p.Val657Asp) c.1778T>A (p.Val593Asp) c.1669T>A n.1544T>A c.1928T>A (p.Val643Asp) c.1748T>A (p.Val583Asp) c.1736T>A (p.Val579Asp) c.1553T>A (p.Val518Asp) | |
| 1 | g.77942771T>C | CA340883307 | NEXN | c.1970T>C (p.Val657Ala) c.1778T>C (p.Val593Ala) c.1669T>C n.1544T>C c.1928T>C (p.Val643Ala) c.1748T>C (p.Val583Ala) c.1736T>C (p.Val579Ala) c.1553T>C (p.Val518Ala) | gnomAD v4 |
| 1 | g.77942771T>G | CA340883308 | NEXN | c.1970T>G (p.Val657Gly) c.1778T>G (p.Val593Gly) c.1669T>G n.1544T>G c.1928T>G (p.Val643Gly) c.1748T>G (p.Val583Gly) c.1736T>G (p.Val579Gly) c.1553T>G (p.Val518Gly) | |
| 1 | g.77942772C>A | CA418709840 | NEXN | c.1971C>A (p.Val657=) c.1779C>A (p.Val593=) c.1670C>A n.1545C>A c.1929C>A (p.Val643=) c.1749C>A (p.Val583=) c.1737C>A (p.Val579=) c.1554C>A (p.Val518=) | gnomAD v4 |
| 1 | g.77942772C>G | CA418709841 | NEXN | c.1971C>G (p.Val657=) c.1779C>G (p.Val593=) c.1670C>G n.1545C>G c.1929C>G (p.Val643=) c.1749C>G (p.Val583=) c.1737C>G (p.Val579=) c.1554C>G (p.Val518=) | |
| 1 | g.77942772C>T | CA418709842 | NEXN | c.1971C>T (p.Val657=) c.1779C>T (p.Val593=) c.1670C>T n.1545C>T c.1929C>T (p.Val643=) c.1749C>T (p.Val583=) c.1737C>T (p.Val579=) c.1554C>T (p.Val518=) | |
| 1 | g.77942773A>C | CA340883309 | NEXN | c.1972A>C (p.Asn658His) c.1780A>C (p.Asn594His) c.1671A>C n.1546A>C c.1930A>C (p.Asn644His) c.1750A>C (p.Asn584His) c.1738A>C (p.Asn580His) c.1555A>C (p.Asn519His) | |
| 1 | g.77942773A>G | CA340883310 | NEXN | c.1972A>G (p.Asn658Asp) c.1780A>G (p.Asn594Asp) c.1671A>G n.1546A>G c.1930A>G (p.Asn644Asp) c.1750A>G (p.Asn584Asp) c.1738A>G (p.Asn580Asp) c.1555A>G (p.Asn519Asp) | |
| 1 | g.77942773A>T | CA340883311 | NEXN | c.1972A>T (p.Asn658Tyr) c.1780A>T (p.Asn594Tyr) c.1671A>T n.1546A>T c.1930A>T (p.Asn644Tyr) c.1750A>T (p.Asn584Tyr) c.1738A>T (p.Asn580Tyr) c.1555A>T (p.Asn519Tyr) | |
| 1 | g.77942774A>C | CA340883312 | NEXN | c.1973A>C (p.Asn658Thr) c.1781A>C (p.Asn594Thr) c.1672A>C n.1547A>C c.1931A>C (p.Asn644Thr) c.1751A>C (p.Asn584Thr) c.1739A>C (p.Asn580Thr) c.1556A>C (p.Asn519Thr) | |
| 1 | g.77942774A>G | CA340883313 | NEXN | c.1973A>G (p.Asn658Ser) c.1781A>G (p.Asn594Ser) c.1672A>G n.1547A>G c.1931A>G (p.Asn644Ser) c.1751A>G (p.Asn584Ser) c.1739A>G (p.Asn580Ser) c.1556A>G (p.Asn519Ser) | ClinVar |
| 1 | g.77942774A>T | CA340883314 | NEXN | c.1973A>T (p.Asn658Ile) c.1781A>T (p.Asn594Ile) c.1672A>T n.1547A>T c.1931A>T (p.Asn644Ile) c.1751A>T (p.Asn584Ile) c.1739A>T (p.Asn580Ile) c.1556A>T (p.Asn519Ile) | |
| 1 | g.77942775C>A | CA340883317 | NEXN | c.1974C>A (p.Asn658Lys) c.1782C>A (p.Asn594Lys) c.1673C>A n.1548C>A c.1932C>A (p.Asn644Lys) c.1752C>A (p.Asn584Lys) c.1740C>A (p.Asn580Lys) c.1557C>A (p.Asn519Lys) | |
| 1 | g.77942775C>G | CA340883315 | NEXN | c.1974C>G (p.Asn658Lys) c.1782C>G (p.Asn594Lys) c.1673C>G n.1548C>G c.1932C>G (p.Asn644Lys) c.1752C>G (p.Asn584Lys) c.1740C>G (p.Asn580Lys) c.1557C>G (p.Asn519Lys) | |
| 1 | g.77942775C>T | CA418709847 | NEXN | c.1974C>T (p.Asn658=) c.1782C>T (p.Asn594=) c.1673C>T n.1548C>T c.1932C>T (p.Asn644=) c.1752C>T (p.Asn584=) c.1740C>T (p.Asn580=) c.1557C>T (p.Asn519=) | dbSNP |
| 1 | g.77942776A>C | CA340883319 | NEXN | c.1975A>C (p.Asn659His) c.1783A>C (p.Asn595His) c.1674A>C n.1549A>C c.1933A>C (p.Asn645His) c.1753A>C (p.Asn585His) c.1741A>C (p.Asn581His) c.1558A>C (p.Asn520His) | |
| 1 | g.77942776A>G | CA340883321 | NEXN | c.1975A>G (p.Asn659Asp) c.1783A>G (p.Asn595Asp) c.1674A>G n.1549A>G c.1933A>G (p.Asn645Asp) c.1753A>G (p.Asn585Asp) c.1741A>G (p.Asn581Asp) c.1558A>G (p.Asn520Asp) | |
| 1 | g.77942776A>T | CA340883322 | NEXN | c.1975A>T (p.Asn659Tyr) c.1783A>T (p.Asn595Tyr) c.1674A>T n.1549A>T c.1933A>T (p.Asn645Tyr) c.1753A>T (p.Asn585Tyr) c.1741A>T (p.Asn581Tyr) c.1558A>T (p.Asn520Tyr) | |
| 1 | g.77942777A= | CA1143720788 | NEXN | c.1976A= (p.Asn659=) c.1784A= (p.Asn595=) c.1675A= n.1550A= c.1934A= (p.Asn645=) c.1754A= (p.Asn585=) c.1742A= (p.Asn581=) c.1559A= (p.Asn520=) | |
| 1 | g.77942777A>C | CA340883324 | NEXN | c.1976A>C (p.Asn659Thr) c.1784A>C (p.Asn595Thr) c.1675A>C n.1550A>C c.1934A>C (p.Asn645Thr) c.1754A>C (p.Asn585Thr) c.1742A>C (p.Asn581Thr) c.1559A>C (p.Asn520Thr) | |
| 1 | g.77942777A>G | CA24692031 | NEXN | c.1976A>G (p.Asn659Ser) c.1784A>G (p.Asn595Ser) c.1675A>G n.1550A>G c.1934A>G (p.Asn645Ser) c.1754A>G (p.Asn585Ser) c.1742A>G (p.Asn581Ser) c.1559A>G (p.Asn520Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77942777A>T | CA340883327 | NEXN | c.1976A>T (p.Asn659Ile) c.1784A>T (p.Asn595Ile) c.1675A>T n.1550A>T c.1934A>T (p.Asn645Ile) c.1754A>T (p.Asn585Ile) c.1742A>T (p.Asn581Ile) c.1559A>T (p.Asn520Ile) | |
| 1 | g.77942778T>A | CA340883329 | NEXN | c.1977T>A (p.Asn659Lys) c.1785T>A (p.Asn595Lys) c.1676T>A n.1551T>A c.1935T>A (p.Asn645Lys) c.1755T>A (p.Asn585Lys) c.1743T>A (p.Asn581Lys) c.1560T>A (p.Asn520Lys) | |
| 1 | g.77942778T>C | CA418709851 | NEXN | c.1977T>C (p.Asn659=) c.1785T>C (p.Asn595=) c.1676T>C n.1551T>C c.1935T>C (p.Asn645=) c.1755T>C (p.Asn585=) c.1743T>C (p.Asn581=) c.1560T>C (p.Asn520=) | |
| 1 | g.77942778T>G | CA340883331 | NEXN | c.1977T>G (p.Asn659Lys) c.1785T>G (p.Asn595Lys) c.1676T>G n.1551T>G c.1935T>G (p.Asn645Lys) c.1755T>G (p.Asn585Lys) c.1743T>G (p.Asn581Lys) c.1560T>G (p.Asn520Lys) | |
| 1 | g.77942779A>C | CA340883333 | NEXN | c.1978A>C (p.Lys660Gln) c.1786A>C (p.Lys596Gln) c.1677A>C n.1552A>C c.1936A>C (p.Lys646Gln) c.1756A>C (p.Lys586Gln) c.1744A>C (p.Lys582Gln) c.1561A>C (p.Lys521Gln) | |
| 1 | g.77942779A>G | CA340883335 | NEXN | c.1978A>G (p.Lys660Glu) c.1786A>G (p.Lys596Glu) c.1677A>G n.1552A>G c.1936A>G (p.Lys646Glu) c.1756A>G (p.Lys586Glu) c.1744A>G (p.Lys582Glu) c.1561A>G (p.Lys521Glu) | |
| 1 | g.77942779A>T | CA340883336 | NEXN | c.1978A>T (p.Lys660Ter) c.1786A>T (p.Lys596Ter) c.1677A>T n.1552A>T c.1936A>T (p.Lys646Ter) c.1756A>T (p.Lys586Ter) c.1744A>T (p.Lys582Ter) c.1561A>T (p.Lys521Ter) | |
| 1 | g.77942780A>C | CA340883338 | NEXN | c.1979A>C (p.Lys660Thr) c.1787A>C (p.Lys596Thr) c.1678A>C n.1553A>C c.1937A>C (p.Lys646Thr) c.1757A>C (p.Lys586Thr) c.1745A>C (p.Lys582Thr) c.1562A>C (p.Lys521Thr) | |
| 1 | g.77942780A>G | CA340883340 | NEXN | c.1979A>G (p.Lys660Arg) c.1787A>G (p.Lys596Arg) c.1678A>G n.1553A>G c.1937A>G (p.Lys646Arg) c.1757A>G (p.Lys586Arg) c.1745A>G (p.Lys582Arg) c.1562A>G (p.Lys521Arg) | |
| 1 | g.77942780A>T | CA340883342 | NEXN | c.1979A>T (p.Lys660Ile) c.1787A>T (p.Lys596Ile) c.1678A>T n.1553A>T c.1937A>T (p.Lys646Ile) c.1757A>T (p.Lys586Ile) c.1745A>T (p.Lys582Ile) c.1562A>T (p.Lys521Ile) | |
| 1 | g.77942781A>C | CA340883344 | NEXN | c.1980A>C (p.Lys660Asn) c.1788A>C (p.Lys596Asn) c.1679A>C n.1554A>C c.1938A>C (p.Lys646Asn) c.1758A>C (p.Lys586Asn) c.1746A>C (p.Lys582Asn) c.1563A>C (p.Lys521Asn) | |
| 1 | g.77942781A>G | CA418709863 | NEXN | c.1980A>G (p.Lys660=) c.1788A>G (p.Lys596=) c.1679A>G n.1554A>G c.1938A>G (p.Lys646=) c.1758A>G (p.Lys586=) c.1746A>G (p.Lys582=) c.1563A>G (p.Lys521=) | |
| 1 | g.77942781A>T | CA340883345 | NEXN | c.1980A>T (p.Lys660Asn) c.1788A>T (p.Lys596Asn) c.1679A>T n.1554A>T c.1938A>T (p.Lys646Asn) c.1758A>T (p.Lys586Asn) c.1746A>T (p.Lys582Asn) c.1563A>T (p.Lys521Asn) | |
| 1 | g.77942782G>A | CA10576435 | NEXN | c.1981G>A (p.Gly661Arg) c.1789G>A (p.Gly597Arg) c.1680G>A n.1555G>A c.1939G>A (p.Gly647Arg) c.1759G>A (p.Gly587Arg) c.1747G>A (p.Gly583Arg) c.1564G>A (p.Gly522Arg) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.77942782G>C | CA340883349 | NEXN | c.1981G>C (p.Gly661Arg) c.1789G>C (p.Gly597Arg) c.1680G>C n.1555G>C c.1939G>C (p.Gly647Arg) c.1759G>C (p.Gly587Arg) c.1747G>C (p.Gly583Arg) c.1564G>C (p.Gly522Arg) | |
| 1 | g.77942782G= | CA1177631470 | NEXN | c.1981G= (p.Gly661=) c.1789G= (p.Gly597=) c.1680G= n.1555G= c.1939G= (p.Gly647=) c.1759G= (p.Gly587=) c.1747G= (p.Gly583=) c.1564G= (p.Gly522=) | |
| 1 | g.77942782G>T | CA340883351 | NEXN | c.1981G>T (p.Gly661Ter) c.1789G>T (p.Gly597Ter) c.1680G>T n.1555G>T c.1939G>T (p.Gly647Ter) c.1759G>T (p.Gly587Ter) c.1747G>T (p.Gly583Ter) c.1564G>T (p.Gly522Ter) | |
| 1 | g.77942783G>A | CA340883353 | NEXN | c.1982G>A (p.Gly661Glu) c.1790G>A (p.Gly597Glu) c.1681G>A n.1556G>A c.1940G>A (p.Gly647Glu) c.1760G>A (p.Gly587Glu) c.1748G>A (p.Gly583Glu) c.1565G>A (p.Gly522Glu) | |
| 1 | g.77942783G>C | CA340883355 | NEXN | c.1982G>C (p.Gly661Ala) c.1790G>C (p.Gly597Ala) c.1681G>C n.1556G>C c.1940G>C (p.Gly647Ala) c.1760G>C (p.Gly587Ala) c.1748G>C (p.Gly583Ala) c.1565G>C (p.Gly522Ala) | |
| 1 | g.77942783G>T | CA340883356 | NEXN | c.1982G>T (p.Gly661Val) c.1790G>T (p.Gly597Val) c.1681G>T n.1556G>T c.1940G>T (p.Gly647Val) c.1760G>T (p.Gly587Val) c.1748G>T (p.Gly583Val) c.1565G>T (p.Gly522Val) | |
| 1 | g.77942784A>C | CA418709865 | NEXN | c.1983A>C (p.Gly661=) c.1791A>C (p.Gly597=) c.1682A>C n.1557A>C c.1941A>C (p.Gly647=) c.1761A>C (p.Gly587=) c.1749A>C (p.Gly583=) c.1566A>C (p.Gly522=) | |
| 1 | g.77942784A>G | CA418709867 | NEXN | c.1983A>G (p.Gly661=) c.1791A>G (p.Gly597=) c.1682A>G n.1557A>G c.1941A>G (p.Gly647=) c.1761A>G (p.Gly587=) c.1749A>G (p.Gly583=) c.1566A>G (p.Gly522=) | |
| 1 | g.77942784A>T | CA418709866 | NEXN | c.1983A>T (p.Gly661=) c.1791A>T (p.Gly597=) c.1682A>T n.1557A>T c.1941A>T (p.Gly647=) c.1761A>T (p.Gly587=) c.1749A>T (p.Gly583=) c.1566A>T (p.Gly522=) | |
| 1 | g.77942785T>A | CA340883662 | NEXN | c.1984T>A (p.Ser662Thr) c.1792T>A (p.Ser598Thr) c.1683T>A n.1558T>A c.1942T>A (p.Ser648Thr) c.1762T>A (p.Ser588Thr) c.1750T>A (p.Ser584Thr) c.1567T>A (p.Ser523Thr) | |
| 1 | g.77942785T>C | CA340883663 | NEXN | c.1984T>C (p.Ser662Pro) c.1792T>C (p.Ser598Pro) c.1683T>C n.1558T>C c.1942T>C (p.Ser648Pro) c.1762T>C (p.Ser588Pro) c.1750T>C (p.Ser584Pro) c.1567T>C (p.Ser523Pro) | |
| 1 | g.77942785T>G | CA340883664 | NEXN | c.1984T>G (p.Ser662Ala) c.1792T>G (p.Ser598Ala) c.1683T>G n.1558T>G c.1942T>G (p.Ser648Ala) c.1762T>G (p.Ser588Ala) c.1750T>G (p.Ser584Ala) c.1567T>G (p.Ser523Ala) | |
| 1 | g.77942786C>A | CA340883666 | NEXN | c.1985C>A (p.Ser662Tyr) c.1793C>A (p.Ser598Tyr) c.1684C>A n.1559C>A c.1943C>A (p.Ser648Tyr) c.1763C>A (p.Ser588Tyr) c.1751C>A (p.Ser584Tyr) c.1568C>A (p.Ser523Tyr) | |
| 1 | g.77942786C= | CA1177631471 | NEXN | c.1985C= (p.Ser662=) c.1793C= (p.Ser598=) c.1684C= n.1559C= c.1943C= (p.Ser648=) c.1763C= (p.Ser588=) c.1751C= (p.Ser584=) c.1568C= (p.Ser523=) | |
| 1 | g.77942786C>G | CA340883668 | NEXN | c.1985C>G (p.Ser662Cys) c.1793C>G (p.Ser598Cys) c.1684C>G n.1559C>G c.1943C>G (p.Ser648Cys) c.1763C>G (p.Ser588Cys) c.1751C>G (p.Ser584Cys) c.1568C>G (p.Ser523Cys) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.77942786C>T | CA340883669 | NEXN | c.1985C>T (p.Ser662Phe) c.1793C>T (p.Ser598Phe) c.1684C>T n.1559C>T c.1943C>T (p.Ser648Phe) c.1763C>T (p.Ser588Phe) c.1751C>T (p.Ser584Phe) c.1568C>T (p.Ser523Phe) | |
| 1 | g.77942787T>A | CA418574038 | NEXN | c.1986T>A (p.Ser662=) c.1794T>A (p.Ser598=) c.1685T>A n.1560T>A c.1944T>A (p.Ser648=) c.1764T>A (p.Ser588=) c.1752T>A (p.Ser584=) c.1569T>A (p.Ser523=) | |
| 1 | g.77942787T>C | CA418574037 | NEXN | c.1986T>C (p.Ser662=) c.1794T>C (p.Ser598=) c.1685T>C n.1560T>C c.1944T>C (p.Ser648=) c.1764T>C (p.Ser588=) c.1752T>C (p.Ser584=) c.1569T>C (p.Ser523=) | |
| 1 | g.77942787T>G | CA418574036 | NEXN | c.1986T>G (p.Ser662=) c.1794T>G (p.Ser598=) c.1685T>G n.1560T>G c.1944T>G (p.Ser648=) c.1764T>G (p.Ser588=) c.1752T>G (p.Ser584=) c.1569T>G (p.Ser523=) | |
| 1 | g.77942788G>A | CA340883674 | NEXN | c.1987G>A (p.Ala663Thr) c.1795G>A (p.Ala599Thr) c.1686G>A n.1561G>A c.1945G>A (p.Ala649Thr) c.1765G>A (p.Ala589Thr) c.1753G>A (p.Ala585Thr) c.1570G>A (p.Ala524Thr) | |
| 1 | g.77942788G>C | CA340883672 | NEXN | c.1987G>C (p.Ala663Pro) c.1795G>C (p.Ala599Pro) c.1686G>C n.1561G>C c.1945G>C (p.Ala649Pro) c.1765G>C (p.Ala589Pro) c.1753G>C (p.Ala585Pro) c.1570G>C (p.Ala524Pro) | COSMIC COSMIC |
| 1 | g.77942788G>T | CA340883670 | NEXN | c.1987G>T (p.Ala663Ser) c.1795G>T (p.Ala599Ser) c.1686G>T n.1561G>T c.1945G>T (p.Ala649Ser) c.1765G>T (p.Ala589Ser) c.1753G>T (p.Ala585Ser) c.1570G>T (p.Ala524Ser) | |
| 1 | g.77942789C>A | CA340883675 | NEXN | c.1988C>A (p.Ala663Glu) c.1796C>A (p.Ala599Glu) c.1687C>A n.1562C>A c.1946C>A (p.Ala649Glu) c.1766C>A (p.Ala589Glu) c.1754C>A (p.Ala585Glu) c.1571C>A (p.Ala524Glu) | |
| 1 | g.77942789C>G | CA340883677 | NEXN | c.1988C>G (p.Ala663Gly) c.1796C>G (p.Ala599Gly) c.1687C>G n.1562C>G c.1946C>G (p.Ala649Gly) c.1766C>G (p.Ala589Gly) c.1754C>G (p.Ala585Gly) c.1571C>G (p.Ala524Gly) | |
| 1 | g.77942789C>T | CA340883676 | NEXN | c.1988C>T (p.Ala663Val) c.1796C>T (p.Ala599Val) c.1687C>T n.1562C>T c.1946C>T (p.Ala649Val) c.1766C>T (p.Ala589Val) c.1754C>T (p.Ala585Val) c.1571C>T (p.Ala524Val) | |
| 1 | g.77942790A= | CA1177631472 | NEXN | c.1989A= (p.Ala663=) c.1797A= (p.Ala599=) c.1688A= n.1563A= c.1947A= (p.Ala649=) c.1767A= (p.Ala589=) c.1755A= (p.Ala585=) c.1572A= (p.Ala524=) | |
| 1 | g.77942790A>C | CA418574039 | NEXN | c.1989A>C (p.Ala663=) c.1797A>C (p.Ala599=) c.1688A>C n.1563A>C c.1947A>C (p.Ala649=) c.1767A>C (p.Ala589=) c.1755A>C (p.Ala585=) c.1572A>C (p.Ala524=) | |
| 1 | g.77942790A>G | CA418574041 | NEXN | c.1989A>G (p.Ala663=) c.1797A>G (p.Ala599=) c.1688A>G n.1563A>G c.1947A>G (p.Ala649=) c.1767A>G (p.Ala589=) c.1755A>G (p.Ala585=) c.1572A>G (p.Ala524=) | |
| 1 | g.77942790A>T | CA418574040 | NEXN | c.1989A>T (p.Ala663=) c.1797A>T (p.Ala599=) c.1688A>T n.1563A>T c.1947A>T (p.Ala649=) c.1767A>T (p.Ala589=) c.1755A>T (p.Ala585=) c.1572A>T (p.Ala524=) | dbSNP |
| 1 | g.77942791G>A | CA340883678 | NEXN | c.1990G>A (p.Ala664Thr) c.1798G>A (p.Ala600Thr) c.1689G>A n.1564G>A c.1948G>A (p.Ala650Thr) c.1768G>A (p.Ala590Thr) c.1756G>A (p.Ala586Thr) c.1573G>A (p.Ala525Thr) | |
| 1 | g.77942791G>C | CA340883682 | NEXN | c.1990G>C (p.Ala664Pro) c.1798G>C (p.Ala600Pro) c.1689G>C n.1564G>C c.1948G>C (p.Ala650Pro) c.1768G>C (p.Ala590Pro) c.1756G>C (p.Ala586Pro) c.1573G>C (p.Ala525Pro) | |
| 1 | g.77942791G>T | CA340883680 | NEXN | c.1990G>T (p.Ala664Ser) c.1798G>T (p.Ala600Ser) c.1689G>T n.1564G>T c.1948G>T (p.Ala650Ser) c.1768G>T (p.Ala590Ser) c.1756G>T (p.Ala586Ser) c.1573G>T (p.Ala525Ser) | |
| 1 | g.77942792C>A | CA340883683 | NEXN | c.1991C>A (p.Ala664Asp) c.1799C>A (p.Ala600Asp) c.1690C>A n.1565C>A c.1949C>A (p.Ala650Asp) c.1769C>A (p.Ala590Asp) c.1757C>A (p.Ala586Asp) c.1574C>A (p.Ala525Asp) | |
| 1 | g.77942792C= | CA1177631473 | NEXN | c.1991C= (p.Ala664=) c.1799C= (p.Ala600=) c.1690C= n.1565C= c.1949C= (p.Ala650=) c.1769C= (p.Ala590=) c.1757C= (p.Ala586=) c.1574C= (p.Ala525=) | |
| 1 | g.77942792C>G | CA340883685 | NEXN | c.1991C>G (p.Ala664Gly) c.1799C>G (p.Ala600Gly) c.1690C>G n.1565C>G c.1949C>G (p.Ala650Gly) c.1769C>G (p.Ala590Gly) c.1757C>G (p.Ala586Gly) c.1574C>G (p.Ala525Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.77942792C>T | CA340883686 | NEXN | c.1991C>T (p.Ala664Val) c.1799C>T (p.Ala600Val) c.1690C>T n.1565C>T c.1949C>T (p.Ala650Val) c.1769C>T (p.Ala590Val) c.1757C>T (p.Ala586Val) c.1574C>T (p.Ala525Val) | |
| 1 | g.77942793T>A | CA418574042 | NEXN | c.1992T>A (p.Ala664=) c.1800T>A (p.Ala600=) c.1691T>A n.1566T>A c.1950T>A (p.Ala650=) c.1770T>A (p.Ala590=) c.1758T>A (p.Ala586=) c.1575T>A (p.Ala525=) | |
| 1 | g.77942793T>C | CA418574043 | NEXN | c.1992T>C (p.Ala664=) c.1800T>C (p.Ala600=) c.1691T>C n.1566T>C c.1950T>C (p.Ala650=) c.1770T>C (p.Ala590=) c.1758T>C (p.Ala586=) c.1575T>C (p.Ala525=) | |
| 1 | g.77942793T>G | CA418574044 | NEXN | c.1992T>G (p.Ala664=) c.1800T>G (p.Ala600=) c.1691T>G n.1566T>G c.1950T>G (p.Ala650=) c.1770T>G (p.Ala590=) c.1758T>G (p.Ala586=) c.1575T>G (p.Ala525=) | |
| 1 | g.77942794A= | CA1177631474 | NEXN | c.1993A= (p.Ser665=) c.1801A= (p.Ser601=) c.1692A= n.1567A= c.1951A= (p.Ser651=) c.1771A= (p.Ser591=) c.1759A= (p.Ser587=) c.1576A= (p.Ser526=) | |
| 1 | g.77942794A>C | CA340883688 | NEXN | c.1993A>C (p.Ser665Arg) c.1801A>C (p.Ser601Arg) c.1692A>C n.1567A>C c.1951A>C (p.Ser651Arg) c.1771A>C (p.Ser591Arg) c.1759A>C (p.Ser587Arg) c.1576A>C (p.Ser526Arg) | |
| 1 | g.77942794A>G | CA340883689 | NEXN | c.1993A>G (p.Ser665Gly) c.1801A>G (p.Ser601Gly) c.1692A>G n.1567A>G c.1951A>G (p.Ser651Gly) c.1771A>G (p.Ser591Gly) c.1759A>G (p.Ser587Gly) c.1576A>G (p.Ser526Gly) | |
| 1 | g.77942794A>T | CA340883691 | NEXN | c.1993A>T (p.Ser665Cys) c.1801A>T (p.Ser601Cys) c.1692A>T n.1567A>T c.1951A>T (p.Ser651Cys) c.1771A>T (p.Ser591Cys) c.1759A>T (p.Ser587Cys) c.1576A>T (p.Ser526Cys) | dbSNP |
| 1 | g.77942795G>A | CA919014 | NEXN | c.1994G>A (p.Ser665Asn) c.1802G>A (p.Ser601Asn) c.1693G>A n.1568G>A c.1952G>A (p.Ser651Asn) c.1772G>A (p.Ser591Asn) c.1760G>A (p.Ser587Asn) c.1577G>A (p.Ser526Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.77942795G>C | CA340883693 | NEXN | c.1994G>C (p.Ser665Thr) c.1802G>C (p.Ser601Thr) c.1693G>C n.1568G>C c.1952G>C (p.Ser651Thr) c.1772G>C (p.Ser591Thr) c.1760G>C (p.Ser587Thr) c.1577G>C (p.Ser526Thr) | |
| 1 | g.77942795G= | CA1177631475 | NEXN | c.1994G= (p.Ser665=) c.1802G= (p.Ser601=) c.1693G= n.1568G= c.1952G= (p.Ser651=) c.1772G= (p.Ser591=) c.1760G= (p.Ser587=) c.1577G= (p.Ser526=) | |
| 1 | g.77942795G>T | CA919015 | NEXN | c.1994G>T (p.Ser665Ile) c.1802G>T (p.Ser601Ile) c.1693G>T n.1568G>T c.1952G>T (p.Ser651Ile) c.1772G>T (p.Ser591Ile) c.1760G>T (p.Ser587Ile) c.1577G>T (p.Ser526Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77942796T>A | CA340883695 | NEXN | c.1995T>A (p.Ser665Arg) c.1803T>A (p.Ser601Arg) c.1694T>A n.1569T>A c.1953T>A (p.Ser651Arg) c.1773T>A (p.Ser591Arg) c.1761T>A (p.Ser587Arg) c.1578T>A (p.Ser526Arg) | |
| 1 | g.77942796T>C | CA919016 | NEXN | c.1995T>C (p.Ser665=) c.1803T>C (p.Ser601=) c.1694T>C n.1569T>C c.1953T>C (p.Ser651=) c.1773T>C (p.Ser591=) c.1761T>C (p.Ser587=) c.1578T>C (p.Ser526=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.77942796T>G | CA340883696 | NEXN | c.1995T>G (p.Ser665Arg) c.1803T>G (p.Ser601Arg) c.1694T>G n.1569T>G c.1953T>G (p.Ser651Arg) c.1773T>G (p.Ser591Arg) c.1761T>G (p.Ser587Arg) c.1578T>G (p.Ser526Arg) | |
| 1 | g.77942796T= | CA1177631476 | NEXN | c.1995T= (p.Ser665=) c.1803T= (p.Ser601=) c.1694T= n.1569T= c.1953T= (p.Ser651=) c.1773T= (p.Ser591=) c.1761T= (p.Ser587=) c.1578T= (p.Ser526=) | |
| 1 | g.77942797A= | CA1143965877 | NEXN | c.1996A= (p.Thr666=) c.1804A= (p.Thr602=) c.1695A= n.1570A= c.1954A= (p.Thr652=) c.1774A= (p.Thr592=) c.1762A= (p.Thr588=) c.1579A= (p.Thr527=) | |
| 1 | g.77942797A>C | CA340883698 | NEXN | c.1996A>C (p.Thr666Pro) c.1804A>C (p.Thr602Pro) c.1695A>C n.1570A>C c.1954A>C (p.Thr652Pro) c.1774A>C (p.Thr592Pro) c.1762A>C (p.Thr588Pro) c.1579A>C (p.Thr527Pro) | |
| 1 | g.77942797A>G | CA142145 | NEXN | c.1996A>G (p.Thr666Ala) c.1804A>G (p.Thr602Ala) c.1695A>G n.1570A>G c.1954A>G (p.Thr652Ala) c.1774A>G (p.Thr592Ala) c.1762A>G (p.Thr588Ala) c.1579A>G (p.Thr527Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77942797A>T | CA340883700 | NEXN | c.1996A>T (p.Thr666Ser) c.1804A>T (p.Thr602Ser) c.1695A>T n.1570A>T c.1954A>T (p.Thr652Ser) c.1774A>T (p.Thr592Ser) c.1762A>T (p.Thr588Ser) c.1579A>T (p.Thr527Ser) | |
| 1 | g.77942798C>A | CA919017 | NEXN | c.1997C>A (p.Thr666Asn) c.1805C>A (p.Thr602Asn) c.1696C>A n.1571C>A c.1955C>A (p.Thr652Asn) c.1775C>A (p.Thr592Asn) c.1763C>A (p.Thr588Asn) c.1580C>A (p.Thr527Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.77942798C= | CA1149104937 | NEXN | c.1997C= (p.Thr666=) c.1805C= (p.Thr602=) c.1696C= n.1571C= c.1955C= (p.Thr652=) c.1775C= (p.Thr592=) c.1763C= (p.Thr588=) c.1580C= (p.Thr527=) | |
| 1 | g.77942798C>G | CA340883703 | NEXN | c.1997C>G (p.Thr666Ser) c.1805C>G (p.Thr602Ser) c.1696C>G n.1571C>G c.1955C>G (p.Thr652Ser) c.1775C>G (p.Thr592Ser) c.1763C>G (p.Thr588Ser) c.1580C>G (p.Thr527Ser) | dbSNP |
| 1 | g.77942798C>T | CA340883702 | NEXN | c.1997C>T (p.Thr666Ile) c.1805C>T (p.Thr602Ile) c.1696C>T n.1571C>T c.1955C>T (p.Thr652Ile) c.1775C>T (p.Thr592Ile) c.1763C>T (p.Thr588Ile) c.1580C>T (p.Thr527Ile) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.77942799C>A | CA418574045 | NEXN | c.1998C>A (p.Thr666=) c.1806C>A (p.Thr602=) c.1697C>A n.1572C>A c.1956C>A (p.Thr652=) c.1776C>A (p.Thr592=) c.1764C>A (p.Thr588=) c.1581C>A (p.Thr527=) | gnomAD v4 |
| 1 | g.77942799C>G | CA418574046 | NEXN | c.1998C>G (p.Thr666=) c.1806C>G (p.Thr602=) c.1697C>G n.1572C>G c.1956C>G (p.Thr652=) c.1776C>G (p.Thr592=) c.1764C>G (p.Thr588=) c.1581C>G (p.Thr527=) | |
| 1 | g.77942799C>T | CA418574047 | NEXN | c.1998C>T (p.Thr666=) c.1806C>T (p.Thr602=) c.1697C>T n.1572C>T c.1956C>T (p.Thr652=) c.1776C>T (p.Thr592=) c.1764C>T (p.Thr588=) c.1581C>T (p.Thr527=) | |
| 1 | g.77942800T>A | CA340883708 | NEXN | c.1999T>A (p.Cys667Ser) c.1807T>A (p.Cys603Ser) c.1698T>A n.1573T>A c.1957T>A (p.Cys653Ser) c.1777T>A (p.Cys593Ser) c.1765T>A (p.Cys589Ser) c.1582T>A (p.Cys528Ser) | |
| 1 | g.77942800T>C | CA340883709 | NEXN | c.1999T>C (p.Cys667Arg) c.1807T>C (p.Cys603Arg) c.1698T>C n.1573T>C c.1957T>C (p.Cys653Arg) c.1777T>C (p.Cys593Arg) c.1765T>C (p.Cys589Arg) c.1582T>C (p.Cys528Arg) | |
| 1 | g.77942800T>G | CA340883710 | NEXN | c.1999T>G (p.Cys667Gly) c.1807T>G (p.Cys603Gly) c.1698T>G n.1573T>G c.1957T>G (p.Cys653Gly) c.1777T>G (p.Cys593Gly) c.1765T>G (p.Cys589Gly) c.1582T>G (p.Cys528Gly) | |
| 1 | g.77942801G>A | CA335448 | NEXN | c.2000G>A (p.Cys667Tyr) c.1808G>A (p.Cys603Tyr) c.1699G>A n.1574G>A c.1958G>A (p.Cys653Tyr) c.1778G>A (p.Cys593Tyr) c.1766G>A (p.Cys589Tyr) c.1583G>A (p.Cys528Tyr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.77942801G>C | CA340883715 | NEXN | c.2000G>C (p.Cys667Ser) c.1808G>C (p.Cys603Ser) c.1699G>C n.1574G>C c.1958G>C (p.Cys653Ser) c.1778G>C (p.Cys593Ser) c.1766G>C (p.Cys589Ser) c.1583G>C (p.Cys528Ser) | |
| 1 | g.77942801G= | CA1177631477 | NEXN | c.2000G= (p.Cys667=) c.1808G= (p.Cys603=) c.1699G= n.1574G= c.1958G= (p.Cys653=) c.1778G= (p.Cys593=) c.1766G= (p.Cys589=) c.1583G= (p.Cys528=) | |
| 1 | g.77942801G>T | CA340883718 | NEXN | c.2000G>T (p.Cys667Phe) c.1808G>T (p.Cys603Phe) c.1699G>T n.1574G>T c.1958G>T (p.Cys653Phe) c.1778G>T (p.Cys593Phe) c.1766G>T (p.Cys589Phe) c.1583G>T (p.Cys528Phe) |