Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.17339528G>A | CA366895004 | AHR | c.1703G>A (p.Gly568Asp) c.1673G>A (p.Gly558Asp) c.1658G>A (p.Gly553Asp) | gnomAD v4 |
7 | g.17339528G>C | CA366895005 | AHR | c.1703G>C (p.Gly568Ala) c.1673G>C (p.Gly558Ala) c.1658G>C (p.Gly553Ala) | |
7 | g.17339528G= | CA1691323864 | AHR | c.1703G= (p.Gly568=) c.1673G= (p.Gly558=) c.1658G= (p.Gly553=) | |
7 | g.17339528G>T | CA366895006 | AHR | c.1703G>T (p.Gly568Val) c.1673G>T (p.Gly558Val) c.1658G>T (p.Gly553Val) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.17339529T>A | CA454134129 | AHR | c.1704T>A (p.Gly568=) c.1674T>A (p.Gly558=) c.1659T>A (p.Gly553=) | |
7 | g.17339529T>C | CA454134130 | AHR | c.1704T>C (p.Gly568=) c.1674T>C (p.Gly558=) c.1659T>C (p.Gly553=) | |
7 | g.17339529T>G | CA454134131 | AHR | c.1704T>G (p.Gly568=) c.1674T>G (p.Gly558=) c.1659T>G (p.Gly553=) | |
7 | g.17339530G>A | CA366895007 | AHR | c.1705G>A (p.Glu569Lys) c.1675G>A (p.Glu559Lys) c.1660G>A (p.Glu554Lys) | COSMIC |
7 | g.17339530G>C | CA366895008 | AHR | c.1705G>C (p.Glu569Gln) c.1675G>C (p.Glu559Gln) c.1660G>C (p.Glu554Gln) | |
7 | g.17339530G>T | CA366895009 | AHR | c.1705G>T (p.Glu569Ter) c.1675G>T (p.Glu559Ter) c.1660G>T (p.Glu554Ter) | |
7 | g.17339531A= | CA1691323865 | AHR | c.1706A= (p.Glu569=) c.1676A= (p.Glu559=) c.1661A= (p.Glu554=) | |
7 | g.17339531A>C | CA366895010 | AHR | c.1706A>C (p.Glu569Ala) c.1676A>C (p.Glu559Ala) c.1661A>C (p.Glu554Ala) | dbSNP |
7 | g.17339531A>G | CA366895011 | AHR | c.1706A>G (p.Glu569Gly) c.1676A>G (p.Glu559Gly) c.1661A>G (p.Glu554Gly) | |
7 | g.17339531A>T | CA366895012 | AHR | c.1706A>T (p.Glu569Val) c.1676A>T (p.Glu559Val) c.1661A>T (p.Glu554Val) | |
7 | g.17339532G>A | CA454134132 | AHR | c.1707G>A (p.Glu569=) c.1677G>A (p.Glu559=) c.1662G>A (p.Glu554=) | gnomAD v4 |
7 | g.17339532G>C | CA366895013 | AHR | c.1707G>C (p.Glu569Asp) c.1677G>C (p.Glu559Asp) c.1662G>C (p.Glu554Asp) | |
7 | g.17339532G>T | CA366895014 | AHR | c.1707G>T (p.Glu569Asp) c.1677G>T (p.Glu559Asp) c.1662G>T (p.Glu554Asp) | |
7 | g.17339533G>A | CA4172168 | AHR | c.1708G>A (p.Val570Ile) c.1678G>A (p.Val560Ile) c.1663G>A (p.Val555Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.17339533G>C | CA366895016 | AHR | c.1708G>C (p.Val570Leu) c.1678G>C (p.Val560Leu) c.1663G>C (p.Val555Leu) | |
7 | g.17339533G= | CA1691323866 | AHR | c.1708G= (p.Val570=) c.1678G= (p.Val560=) c.1663G= (p.Val555=) | |
7 | g.17339533G>T | CA366895015 | AHR | c.1708G>T (p.Val570Phe) c.1678G>T (p.Val560Phe) c.1663G>T (p.Val555Phe) | |
7 | g.17339534T>A | CA366895017 | AHR | c.1709T>A (p.Val570Asp) c.1679T>A (p.Val560Asp) c.1664T>A (p.Val555Asp) | |
7 | g.17339534T>C | CA4172169 | AHR | c.1709T>C (p.Val570Ala) c.1679T>C (p.Val560Ala) c.1664T>C (p.Val555Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.17339534T>G | CA366895018 | AHR | c.1709T>G (p.Val570Gly) c.1679T>G (p.Val560Gly) c.1664T>G (p.Val555Gly) | |
7 | g.17339534T= | CA1691323867 | AHR | c.1709T= (p.Val570=) c.1679T= (p.Val560=) c.1664T= (p.Val555=) | |
7 | g.17339535T>A | CA454134135 | AHR | c.1710T>A (p.Val570=) c.1680T>A (p.Val560=) c.1665T>A (p.Val555=) | |
7 | g.17339535T>C | CA454134134 | AHR | c.1710T>C (p.Val570=) c.1680T>C (p.Val560=) c.1665T>C (p.Val555=) | |
7 | g.17339535T>G | CA454134133 | AHR | c.1710T>G (p.Val570=) c.1680T>G (p.Val560=) c.1665T>G (p.Val555=) | COSMIC |
7 | g.17339536G>A | CA154120771 | AHR | c.1711G>A (p.Asp571Asn) c.1681G>A (p.Asp561Asn) c.1666G>A (p.Asp556Asn) | ClinVar dbSNP |
7 | g.17339536G>C | CA366895019 | AHR | c.1711G>C (p.Asp571His) c.1681G>C (p.Asp561His) c.1666G>C (p.Asp556His) | |
7 | g.17339536G= | CA1691323868 | AHR | c.1711G= (p.Asp571=) c.1681G= (p.Asp561=) c.1666G= (p.Asp556=) | |
7 | g.17339536G>T | CA366895020 | AHR | c.1711G>T (p.Asp571Tyr) c.1681G>T (p.Asp561Tyr) c.1666G>T (p.Asp556Tyr) | gnomAD v4 |
7 | g.17339537A>C | CA366895021 | AHR | c.1712A>C (p.Asp571Ala) c.1682A>C (p.Asp561Ala) c.1667A>C (p.Asp556Ala) | |
7 | g.17339537A>G | CA366895022 | AHR | c.1712A>G (p.Asp571Gly) c.1682A>G (p.Asp561Gly) c.1667A>G (p.Asp556Gly) | |
7 | g.17339537A>T | CA366895023 | AHR | c.1712A>T (p.Asp571Val) c.1682A>T (p.Asp561Val) c.1667A>T (p.Asp556Val) | |
7 | g.17339538C>A | CA366895024 | AHR | c.1713C>A (p.Asp571Glu) c.1683C>A (p.Asp561Glu) c.1668C>A (p.Asp556Glu) | gnomAD v4 |
7 | g.17339538C= | CA1691323869 | AHR | c.1713C= (p.Asp571=) c.1683C= (p.Asp561=) c.1668C= (p.Asp556=) | |
7 | g.17339538C>G | CA4172170 | AHR | c.1713C>G (p.Asp571Glu) c.1683C>G (p.Asp561Glu) c.1668C>G (p.Asp556Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.17339538C>T | CA454134136 | AHR | c.1713C>T (p.Asp571=) c.1683C>T (p.Asp561=) c.1668C>T (p.Asp556=) | |
7 | g.17339539T>A | CA366895025 | AHR | c.1714T>A (p.Phe572Ile) c.1684T>A (p.Phe562Ile) c.1669T>A (p.Phe557Ile) | |
7 | g.17339539T>C | CA366895026 | AHR | c.1714T>C (p.Phe572Leu) c.1684T>C (p.Phe562Leu) c.1669T>C (p.Phe557Leu) | ClinVar dbSNP |
7 | g.17339539T>G | CA366895027 | AHR | c.1714T>G (p.Phe572Val) c.1684T>G (p.Phe562Val) c.1669T>G (p.Phe557Val) | gnomAD v4 |
7 | g.17339539T= | CA1691323870 | AHR | c.1714T= (p.Phe572=) c.1684T= (p.Phe562=) c.1669T= (p.Phe557=) | |
7 | g.17339540T>A | CA366895029 | AHR | c.1715T>A (p.Phe572Tyr) c.1685T>A (p.Phe562Tyr) c.1670T>A (p.Phe557Tyr) | |
7 | g.17339540T>C | CA366895030 | AHR | c.1715T>C (p.Phe572Ser) c.1685T>C (p.Phe562Ser) c.1670T>C (p.Phe557Ser) | |
7 | g.17339540T>G | CA366895028 | AHR | c.1715T>G (p.Phe572Cys) c.1685T>G (p.Phe562Cys) c.1670T>G (p.Phe557Cys) | |
7 | g.17339541C>A | CA366895031 | AHR | c.1716C>A (p.Phe572Leu) c.1686C>A (p.Phe562Leu) c.1671C>A (p.Phe557Leu) | |
7 | g.17339541C>G | CA366895032 | AHR | c.1716C>G (p.Phe572Leu) c.1686C>G (p.Phe562Leu) c.1671C>G (p.Phe557Leu) | |
7 | g.17339541C>T | CA454134137 | AHR | c.1716C>T (p.Phe572=) c.1686C>T (p.Phe562=) c.1671C>T (p.Phe557=) | |
7 | g.17339542A>C | CA454134138 | AHR | c.1717A>C (p.Arg573=) c.1687A>C (p.Arg563=) c.1672A>C (p.Arg558=) | |
7 | g.17339542A>G | CA366895033 | AHR | c.1717A>G (p.Arg573Gly) c.1687A>G (p.Arg563Gly) c.1672A>G (p.Arg558Gly) | gnomAD v4 |
7 | g.17339542A>T | CA366895034 | AHR | c.1717A>T (p.Arg573Ter) c.1687A>T (p.Arg563Ter) c.1672A>T (p.Arg558Ter) | |
7 | g.17339543G>A | CA366895035 | AHR | c.1718G>A (p.Arg573Lys) c.1688G>A (p.Arg563Lys) c.1673G>A (p.Arg558Lys) | |
7 | g.17339543G>C | CA366895036 | AHR | c.1718G>C (p.Arg573Thr) c.1688G>C (p.Arg563Thr) c.1673G>C (p.Arg558Thr) | gnomAD v4 |
7 | g.17339543G>T | CA366895037 | AHR | c.1718G>T (p.Arg573Ile) c.1688G>T (p.Arg563Ile) c.1673G>T (p.Arg558Ile) | |
7 | g.17339544A>C | CA366895038 | AHR | c.1719A>C (p.Arg573Ser) c.1689A>C (p.Arg563Ser) c.1674A>C (p.Arg558Ser) | |
7 | g.17339544A>G | CA454134139 | AHR | c.1719A>G (p.Arg573=) c.1689A>G (p.Arg563=) c.1674A>G (p.Arg558=) | |
7 | g.17339544A>T | CA366895039 | AHR | c.1719A>T (p.Arg573Ser) c.1689A>T (p.Arg563Ser) c.1674A>T (p.Arg558Ser) | |
7 | g.17339545G>A | CA366895040 | AHR | c.1720G>A (p.Asp574Asn) c.1690G>A (p.Asp564Asn) c.1675G>A (p.Asp559Asn) | COSMIC |
7 | g.17339545G>C | CA366895041 | AHR | c.1720G>C (p.Asp574His) c.1690G>C (p.Asp564His) c.1675G>C (p.Asp559His) | gnomAD v4 |
7 | g.17339545G>T | CA366895042 | AHR | c.1720G>T (p.Asp574Tyr) c.1690G>T (p.Asp564Tyr) c.1675G>T (p.Asp559Tyr) | gnomAD v4 |
7 | g.17339546A>C | CA366895045 | AHR | c.1721A>C (p.Asp574Ala) c.1691A>C (p.Asp564Ala) c.1676A>C (p.Asp559Ala) | |
7 | g.17339546A>G | CA366895043 | AHR | c.1721A>G (p.Asp574Gly) c.1691A>G (p.Asp564Gly) c.1676A>G (p.Asp559Gly) | |
7 | g.17339546A>T | CA366895044 | AHR | c.1721A>T (p.Asp574Val) c.1691A>T (p.Asp564Val) c.1676A>T (p.Asp559Val) | |
7 | g.17339547C>A | CA366895046 | AHR | c.1722C>A (p.Asp574Glu) c.1692C>A (p.Asp564Glu) c.1677C>A (p.Asp559Glu) | |
7 | g.17339547C>G | CA366895047 | AHR | c.1722C>G (p.Asp574Glu) c.1692C>G (p.Asp564Glu) c.1677C>G (p.Asp559Glu) | |
7 | g.17339547C>T | CA454134140 | AHR | c.1722C>T (p.Asp574=) c.1692C>T (p.Asp564=) c.1677C>T (p.Asp559=) | |
7 | g.17339548A>C | CA366895048 | AHR | c.1723A>C (p.Ile575Leu) c.1693A>C (p.Ile565Leu) c.1678A>C (p.Ile560Leu) | |
7 | g.17339548A>G | CA366895049 | AHR | c.1723A>G (p.Ile575Val) c.1693A>G (p.Ile565Val) c.1678A>G (p.Ile560Val) | gnomAD v4 |
7 | g.17339548A>T | CA366895050 | AHR | c.1723A>T (p.Ile575Phe) c.1693A>T (p.Ile565Phe) c.1678A>T (p.Ile560Phe) | |
7 | g.17339549T>A | CA366895051 | AHR | c.1724T>A (p.Ile575Asn) c.1694T>A (p.Ile565Asn) c.1679T>A (p.Ile560Asn) | |
7 | g.17339549T>C | CA4172171 | AHR | c.1724T>C (p.Ile575Thr) c.1694T>C (p.Ile565Thr) c.1679T>C (p.Ile560Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.17339549T>G | CA366895052 | AHR | c.1724T>G (p.Ile575Ser) c.1694T>G (p.Ile565Ser) c.1679T>G (p.Ile560Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.17339549T= | CA1691323871 | AHR | c.1724T= (p.Ile575=) c.1694T= (p.Ile565=) c.1679T= (p.Ile560=) | |
7 | g.17339550T>A | CA454134141 | AHR | c.1725T>A (p.Ile575=) c.1695T>A (p.Ile565=) c.1680T>A (p.Ile560=) | |
7 | g.17339550T>C | CA454134142 | AHR | c.1725T>C (p.Ile575=) c.1695T>C (p.Ile565=) c.1680T>C (p.Ile560=) | |
7 | g.17339550T>G | CA366895053 | AHR | c.1725T>G (p.Ile575Met) c.1695T>G (p.Ile565Met) c.1680T>G (p.Ile560Met) | |
7 | g.17339551G>A | CA366895054 | AHR | c.1726G>A (p.Asp576Asn) c.1696G>A (p.Asp566Asn) c.1681G>A (p.Asp561Asn) | |
7 | g.17339551G>C | CA154120797 | AHR | c.1726G>C (p.Asp576His) c.1696G>C (p.Asp566His) c.1681G>C (p.Asp561His) | dbSNP |
7 | g.17339551G= | CA1691323872 | AHR | c.1726G= (p.Asp576=) c.1696G= (p.Asp566=) c.1681G= (p.Asp561=) | |
7 | g.17339551G>T | CA366895055 | AHR | c.1726G>T (p.Asp576Tyr) c.1696G>T (p.Asp566Tyr) c.1681G>T (p.Asp561Tyr) | gnomAD v4 |
7 | g.17339552A>C | CA366895057 | AHR | c.1727A>C (p.Asp576Ala) c.1697A>C (p.Asp566Ala) c.1682A>C (p.Asp561Ala) | |
7 | g.17339552A>G | CA366895058 | AHR | c.1727A>G (p.Asp576Gly) c.1697A>G (p.Asp566Gly) c.1682A>G (p.Asp561Gly) | |
7 | g.17339552A>T | CA366895056 | AHR | c.1727A>T (p.Asp576Val) c.1697A>T (p.Asp566Val) c.1682A>T (p.Asp561Val) | |
7 | g.17339553C>A | CA366895059 | AHR | c.1728C>A (p.Asp576Glu) c.1698C>A (p.Asp566Glu) c.1683C>A (p.Asp561Glu) | |
7 | g.17339553C= | CA1691323873 | AHR | c.1728C= (p.Asp576=) c.1698C= (p.Asp566=) c.1683C= (p.Asp561=) | |
7 | g.17339553C>G | CA366895060 | AHR | c.1728C>G (p.Asp576Glu) c.1698C>G (p.Asp566Glu) c.1683C>G (p.Asp561Glu) | gnomAD v4 |
7 | g.17339553C>T | CA154120807 | AHR | c.1728C>T (p.Asp576=) c.1698C>T (p.Asp566=) c.1683C>T (p.Asp561=) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.17339554T>A | CA366895061 | AHR | c.1729T>A (p.Leu577Ile) c.1699T>A (p.Leu567Ile) c.1684T>A (p.Leu562Ile) | |
7 | g.17339554T>C | CA454134143 | AHR | c.1729T>C (p.Leu577=) c.1699T>C (p.Leu567=) c.1684T>C (p.Leu562=) | |
7 | g.17339554T>G | CA366895062 | AHR | c.1729T>G (p.Leu577Val) c.1699T>G (p.Leu567Val) c.1684T>G (p.Leu562Val) | |
7 | g.17339555T>A | CA366895063 | AHR | c.1730T>A (p.Leu577Ter) c.1700T>A (p.Leu567Ter) c.1685T>A (p.Leu562Ter) | |
7 | g.17339555T>C | CA366895065 | AHR | c.1730T>C (p.Leu577Ser) c.1700T>C (p.Leu567Ser) c.1685T>C (p.Leu562Ser) | |
7 | g.17339555T>G | CA366895064 | AHR | c.1730T>G (p.Leu577Ter) c.1700T>G (p.Leu567Ter) c.1685T>G (p.Leu562Ter) | |
7 | g.17339556A>C | CA366895066 | AHR | c.1731A>C (p.Leu577Phe) c.1701A>C (p.Leu567Phe) c.1686A>C (p.Leu562Phe) | |
7 | g.17339556A>G | CA454134144 | AHR | c.1731A>G (p.Leu577=) c.1701A>G (p.Leu567=) c.1686A>G (p.Leu562=) | |
7 | g.17339556A>T | CA366895067 | AHR | c.1731A>T (p.Leu577Phe) c.1701A>T (p.Leu567Phe) c.1686A>T (p.Leu562Phe) | |
7 | g.17339557A= | CA1691323874 | AHR | c.1732A= (p.Thr578=) c.1702A= (p.Thr568=) c.1687A= (p.Thr563=) | |
7 | g.17339557A>C | CA366895068 | AHR | c.1732A>C (p.Thr578Pro) c.1702A>C (p.Thr568Pro) c.1687A>C (p.Thr563Pro) | |
7 | g.17339557A>G | CA366895069 | AHR | c.1732A>G (p.Thr578Ala) c.1702A>G (p.Thr568Ala) c.1687A>G (p.Thr563Ala) | |
7 | g.17339557A>T | CA4172172 | AHR | c.1732A>T (p.Thr578Ser) c.1702A>T (p.Thr568Ser) c.1687A>T (p.Thr563Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.17339558C>A | CA366895070 | AHR | c.1733C>A (p.Thr578Lys) c.1703C>A (p.Thr568Lys) c.1688C>A (p.Thr563Lys) | |
7 | g.17339558C= | CA1691323875 | AHR | c.1733C= (p.Thr578=) c.1703C= (p.Thr568=) c.1688C= (p.Thr563=) | |
7 | g.17339558C>G | CA366895071 | AHR | c.1733C>G (p.Thr578Arg) c.1703C>G (p.Thr568Arg) c.1688C>G (p.Thr563Arg) | |
7 | g.17339558C>T | CA4172173 | AHR | c.1733C>T (p.Thr578Met) c.1703C>T (p.Thr568Met) c.1688C>T (p.Thr563Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
7 | g.17339559G>A | CA4172174 | AHR | c.1734G>A (p.Thr578=) c.1704G>A (p.Thr568=) c.1689G>A (p.Thr563=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.17339559G>C | CA454134145 | AHR | c.1734G>C (p.Thr578=) c.1704G>C (p.Thr568=) c.1689G>C (p.Thr563=) | |
7 | g.17339559G= | CA1691323876 | AHR | c.1734G= (p.Thr578=) c.1704G= (p.Thr568=) c.1689G= (p.Thr563=) | |
7 | g.17339559G>T | CA454134146 | AHR | c.1734G>T (p.Thr578=) c.1704G>T (p.Thr568=) c.1689G>T (p.Thr563=) | |
7 | g.17339560G>A | CA366895072 | AHR | c.1735G>A (p.Asp579Asn) c.1705G>A (p.Asp569Asn) c.1690G>A (p.Asp564Asn) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.17339560G>C | CA366895073 | AHR | c.1735G>C (p.Asp579His) c.1705G>C (p.Asp569His) c.1690G>C (p.Asp564His) | |
7 | g.17339560G= | CA1691323877 | AHR | c.1735G= (p.Asp579=) c.1705G= (p.Asp569=) c.1690G= (p.Asp564=) | |
7 | g.17339560G>T | CA366895074 | AHR | c.1735G>T (p.Asp579Tyr) c.1705G>T (p.Asp569Tyr) c.1690G>T (p.Asp564Tyr) | |
7 | g.17339561A>C | CA366895077 | AHR | c.1736A>C (p.Asp579Ala) c.1706A>C (p.Asp569Ala) c.1691A>C (p.Asp564Ala) | |
7 | g.17339561A>G | CA366895075 | AHR | c.1736A>G (p.Asp579Gly) c.1706A>G (p.Asp569Gly) c.1691A>G (p.Asp564Gly) | |
7 | g.17339561A>T | CA366895076 | AHR | c.1736A>T (p.Asp579Val) c.1706A>T (p.Asp569Val) c.1691A>T (p.Asp564Val) | |
7 | g.17339562T>A | CA366895078 | AHR | c.1737T>A (p.Asp579Glu) c.1707T>A (p.Asp569Glu) c.1692T>A (p.Asp564Glu) | |
7 | g.17339562T>C | CA154120821 | AHR | c.1737T>C (p.Asp579=) c.1707T>C (p.Asp569=) c.1692T>C (p.Asp564=) | dbSNP gnomAD v4 |
7 | g.17339562T>G | CA366895079 | AHR | c.1737T>G (p.Asp579Glu) c.1707T>G (p.Asp569Glu) c.1692T>G (p.Asp564Glu) | |
7 | g.17339562T= | CA1691323878 | AHR | c.1737T= (p.Asp579=) c.1707T= (p.Asp569=) c.1692T= (p.Asp564=) | |
7 | g.17339563G>A | CA366895080 | AHR | c.1738G>A (p.Glu580Lys) c.1708G>A (p.Glu570Lys) c.1693G>A (p.Glu565Lys) | |
7 | g.17339563G>C | CA366895081 | AHR | c.1738G>C (p.Glu580Gln) c.1708G>C (p.Glu570Gln) c.1693G>C (p.Glu565Gln) | |
7 | g.17339563G>T | CA366895082 | AHR | c.1738G>T (p.Glu580Ter) c.1708G>T (p.Glu570Ter) c.1693G>T (p.Glu565Ter) | gnomAD v4 COSMIC |
7 | g.17339564A>C | CA366895083 | AHR | c.1739A>C (p.Glu580Ala) c.1709A>C (p.Glu570Ala) c.1694A>C (p.Glu565Ala) | |
7 | g.17339564A>G | CA366895084 | AHR | c.1739A>G (p.Glu580Gly) c.1709A>G (p.Glu570Gly) c.1694A>G (p.Glu565Gly) | |
7 | g.17339564A>T | CA366895085 | AHR | c.1739A>T (p.Glu580Val) c.1709A>T (p.Glu570Val) c.1694A>T (p.Glu565Val) | |
7 | g.17339566del | CA2681909911 | AHR | c.1741del (p.Ile581SerfsTer2) c.1711del (p.Ile571SerfsTer2) c.1696del (p.Ile566SerfsTer2) | gnomAD v4 |
7 | g.17339565A= | CA1691323879 | AHR | c.1740A= (p.Glu580=) c.1710A= (p.Glu570=) c.1695A= (p.Glu565=) | |
7 | g.17339565A>C | CA366895086 | AHR | c.1740A>C (p.Glu580Asp) c.1710A>C (p.Glu570Asp) c.1695A>C (p.Glu565Asp) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.17339565A>G | CA454134147 | AHR | c.1740A>G (p.Glu580=) c.1710A>G (p.Glu570=) c.1695A>G (p.Glu565=) | |
7 | g.17339565A>T | CA366895087 | AHR | c.1740A>T (p.Glu580Asp) c.1710A>T (p.Glu570Asp) c.1695A>T (p.Glu565Asp) | |
7 | g.17339566A>C | CA366895090 | AHR | c.1741A>C (p.Ile581Leu) c.1711A>C (p.Ile571Leu) c.1696A>C (p.Ile566Leu) | |
7 | g.17339566A>G | CA366895089 | AHR | c.1741A>G (p.Ile581Val) c.1711A>G (p.Ile571Val) c.1696A>G (p.Ile566Val) | |
7 | g.17339566A>T | CA366895088 | AHR | c.1741A>T (p.Ile581Phe) c.1711A>T (p.Ile571Phe) c.1696A>T (p.Ile566Phe) | |
7 | g.17339567T>A | CA366895091 | AHR | c.1742T>A (p.Ile581Asn) c.1712T>A (p.Ile571Asn) c.1697T>A (p.Ile566Asn) | gnomAD v4 |
7 | g.17339567T>C | CA366895092 | AHR | c.1742T>C (p.Ile581Thr) c.1712T>C (p.Ile571Thr) c.1697T>C (p.Ile566Thr) | |
7 | g.17339567T>G | CA366895093 | AHR | c.1742T>G (p.Ile581Ser) c.1712T>G (p.Ile571Ser) c.1697T>G (p.Ile566Ser) | |
7 | g.17339567_17339568delinsAT | CA2580076907 | AHR | c.1742_1743delinsAT (p.Ile581Asn) c.1712_1713delinsAT (p.Ile571Asn) c.1697_1698delinsAT (p.Ile566Asn) | ClinVar |
7 | g.17339568C>A | CA154120829 | AHR | c.1743C>A (p.Ile581=) c.1713C>A (p.Ile571=) c.1698C>A (p.Ile566=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.17339568C= | CA1691323880 | AHR | c.1743C= (p.Ile581=) c.1713C= (p.Ile571=) c.1698C= (p.Ile566=) | |
7 | g.17339568C>G | CA366895094 | AHR | c.1743C>G (p.Ile581Met) c.1713C>G (p.Ile571Met) c.1698C>G (p.Ile566Met) | |
7 | g.17339568C>T | CA454134148 | AHR | c.1743C>T (p.Ile581=) c.1713C>T (p.Ile571=) c.1698C>T (p.Ile566=) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.17339569C>A | CA366895095 | AHR | c.1744C>A (p.Leu582Met) c.1714C>A (p.Leu572Met) c.1699C>A (p.Leu567Met) | ClinVar dbSNP gnomAD v4 |
7 | g.17339569C= | CA1691323881 | AHR | c.1744C= (p.Leu582=) c.1714C= (p.Leu572=) c.1699C= (p.Leu567=) | |
7 | g.17339569C>G | CA366895096 | AHR | c.1744C>G (p.Leu582Val) c.1714C>G (p.Leu572Val) c.1699C>G (p.Leu567Val) | dbSNP |
7 | g.17339569C>T | CA454134149 | AHR | c.1744C>T (p.Leu582=) c.1714C>T (p.Leu572=) c.1699C>T (p.Leu567=) | |
7 | g.17339570T>A | CA366895097 | AHR | c.1745T>A (p.Leu582Gln) c.1715T>A (p.Leu572Gln) c.1700T>A (p.Leu567Gln) | |
7 | g.17339570T>C | CA366895098 | AHR | c.1745T>C (p.Leu582Pro) c.1715T>C (p.Leu572Pro) c.1700T>C (p.Leu567Pro) | |
7 | g.17339570T>G | CA366895099 | AHR | c.1745T>G (p.Leu582Arg) c.1715T>G (p.Leu572Arg) c.1700T>G (p.Leu567Arg) | |
7 | g.17339571G>A | CA454134152 | AHR | c.1746G>A (p.Leu582=) c.1716G>A (p.Leu572=) c.1701G>A (p.Leu567=) | |
7 | g.17339571G>C | CA454134151 | AHR | c.1746G>C (p.Leu582=) c.1716G>C (p.Leu572=) c.1701G>C (p.Leu567=) | |
7 | g.17339571G>T | CA454134150 | AHR | c.1746G>T (p.Leu582=) c.1716G>T (p.Leu572=) c.1701G>T (p.Leu567=) | |
7 | g.17339572A>C | CA366895100 | AHR | c.1747A>C (p.Thr583Pro) c.1717A>C (p.Thr573Pro) c.1702A>C (p.Thr568Pro) | |
7 | g.17339572A>G | CA366895101 | AHR | c.1747A>G (p.Thr583Ala) c.1717A>G (p.Thr573Ala) c.1702A>G (p.Thr568Ala) | gnomAD v4 |
7 | g.17339572A>T | CA366895102 | AHR | c.1747A>T (p.Thr583Ser) c.1717A>T (p.Thr573Ser) c.1702A>T (p.Thr568Ser) | |
7 | g.17339573C>A | CA366895104 | AHR | c.1748C>A (p.Thr583Lys) c.1718C>A (p.Thr573Lys) c.1703C>A (p.Thr568Lys) | |
7 | g.17339573C= | CA1691323882 | AHR | c.1748C= (p.Thr583=) c.1718C= (p.Thr573=) c.1703C= (p.Thr568=) | |
7 | g.17339573C>G | CA366895103 | AHR | c.1748C>G (p.Thr583Arg) c.1718C>G (p.Thr573Arg) c.1703C>G (p.Thr568Arg) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.17339573C>T | CA4172175 | AHR | c.1748C>T (p.Thr583Met) c.1718C>T (p.Thr573Met) c.1703C>T (p.Thr568Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.17339574G>A | CA4172176 | AHR | c.1749G>A (p.Thr583=) c.1719G>A (p.Thr573=) c.1704G>A (p.Thr568=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.17339574G>C | CA154120837 | AHR | c.1749G>C (p.Thr583=) c.1719G>C (p.Thr573=) c.1704G>C (p.Thr568=) | dbSNP gnomAD v4 |
7 | g.17339574G= | CA1691323883 | AHR | c.1749G= (p.Thr583=) c.1719G= (p.Thr573=) c.1704G= (p.Thr568=) | |
7 | g.17339574G>T | CA454134153 | AHR | c.1749G>T (p.Thr583=) c.1719G>T (p.Thr573=) c.1704G>T (p.Thr568=) | |
7 | g.17339575T>A | CA366895105 | AHR | c.1750T>A (p.Tyr584Asn) c.1720T>A (p.Tyr574Asn) c.1705T>A (p.Tyr569Asn) | |
7 | g.17339575T>C | CA366895106 | AHR | c.1750T>C (p.Tyr584His) c.1720T>C (p.Tyr574His) c.1705T>C (p.Tyr569His) | |
7 | g.17339575T>G | CA366895107 | AHR | c.1750T>G (p.Tyr584Asp) c.1720T>G (p.Tyr574Asp) c.1705T>G (p.Tyr569Asp) | dbSNP |
7 | g.17339575T= | CA1691323884 | AHR | c.1750T= (p.Tyr584=) c.1720T= (p.Tyr574=) c.1705T= (p.Tyr569=) | |
7 | g.17339576A>C | CA366895108 | AHR | c.1751A>C (p.Tyr584Ser) c.1721A>C (p.Tyr574Ser) c.1706A>C (p.Tyr569Ser) | |
7 | g.17339576A>G | CA366895109 | AHR | c.1751A>G (p.Tyr584Cys) c.1721A>G (p.Tyr574Cys) c.1706A>G (p.Tyr569Cys) | gnomAD v4 |
7 | g.17339576A>T | CA366895110 | AHR | c.1751A>T (p.Tyr584Phe) c.1721A>T (p.Tyr574Phe) c.1706A>T (p.Tyr569Phe) | gnomAD v4 |
7 | g.17339577T>A | CA366895111 | AHR | c.1752T>A (p.Tyr584Ter) c.1722T>A (p.Tyr574Ter) c.1707T>A (p.Tyr569Ter) | |
7 | g.17339577T>C | CA454134154 | AHR | c.1752T>C (p.Tyr584=) c.1722T>C (p.Tyr574=) c.1707T>C (p.Tyr569=) | |
7 | g.17339577T>G | CA366895112 | AHR | c.1752T>G (p.Tyr584Ter) c.1722T>G (p.Tyr574Ter) c.1707T>G (p.Tyr569Ter) | |
7 | g.17339578G>A | CA366895113 | AHR | c.1753G>A (p.Val585Ile) c.1723G>A (p.Val575Ile) c.1708G>A (p.Val570Ile) | dbSNP gnomAD v4 |
7 | g.17339578G>C | CA366895114 | AHR | c.1753G>C (p.Val585Leu) c.1723G>C (p.Val575Leu) c.1708G>C (p.Val570Leu) | gnomAD v4 |
7 | g.17339578G= | CA1691323885 | AHR | c.1753G= (p.Val585=) c.1723G= (p.Val575=) c.1708G= (p.Val570=) | |
7 | g.17339578G>T | CA366895115 | AHR | c.1753G>T (p.Val585Phe) c.1723G>T (p.Val575Phe) c.1708G>T (p.Val570Phe) | |
7 | g.17339579T>A | CA366895118 | AHR | c.1754T>A (p.Val585Asp) c.1724T>A (p.Val575Asp) c.1709T>A (p.Val570Asp) | |
7 | g.17339579T>C | CA366895117 | AHR | c.1754T>C (p.Val585Ala) c.1724T>C (p.Val575Ala) c.1709T>C (p.Val570Ala) | gnomAD v4 |
7 | g.17339579T>G | CA366895116 | AHR | c.1754T>G (p.Val585Gly) c.1724T>G (p.Val575Gly) c.1709T>G (p.Val570Gly) | |
7 | g.17339580C>A | CA454134155 | AHR | c.1755C>A (p.Val585=) c.1725C>A (p.Val575=) c.1710C>A (p.Val570=) | gnomAD v4 |
7 | g.17339580C= | CA1691323886 | AHR | c.1755C= (p.Val585=) c.1725C= (p.Val575=) c.1710C= (p.Val570=) | |
7 | g.17339580C>G | CA454134156 | AHR | c.1755C>G (p.Val585=) c.1725C>G (p.Val575=) c.1710C>G (p.Val570=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.17339580C>T | CA4172177 | AHR | c.1755C>T (p.Val585=) c.1725C>T (p.Val575=) c.1710C>T (p.Val570=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.17339581C>A | CA366895119 | AHR | c.1756C>A (p.Gln586Lys) c.1726C>A (p.Gln576Lys) c.1711C>A (p.Gln571Lys) | |
7 | g.17339581C>G | CA366895121 | AHR | c.1756C>G (p.Gln586Glu) c.1726C>G (p.Gln576Glu) c.1711C>G (p.Gln571Glu) | |
7 | g.17339581C>T | CA366895120 | AHR | c.1756C>T (p.Gln586Ter) c.1726C>T (p.Gln576Ter) c.1711C>T (p.Gln571Ter) | |
7 | g.17339582A>C | CA366895122 | AHR | c.1757A>C (p.Gln586Pro) c.1727A>C (p.Gln576Pro) c.1712A>C (p.Gln571Pro) | |
7 | g.17339582A>G | CA366895123 | AHR | c.1757A>G (p.Gln586Arg) c.1727A>G (p.Gln576Arg) c.1712A>G (p.Gln571Arg) | |
7 | g.17339582A>T | CA366895124 | AHR | c.1757A>T (p.Gln586Leu) c.1727A>T (p.Gln576Leu) c.1712A>T (p.Gln571Leu) | |
7 | g.17339583A= | CA1691323887 | AHR | c.1758A= (p.Gln586=) c.1728A= (p.Gln576=) c.1713A= (p.Gln571=) | |
7 | g.17339583A>C | CA4172178 | AHR | c.1758A>C (p.Gln586His) c.1728A>C (p.Gln576His) c.1713A>C (p.Gln571His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.17339583A>G | CA454134157 | AHR | c.1758A>G (p.Gln586=) c.1728A>G (p.Gln576=) c.1713A>G (p.Gln571=) | gnomAD v4 |
7 | g.17339583A>T | CA366895125 | AHR | c.1758A>T (p.Gln586His) c.1728A>T (p.Gln576His) c.1713A>T (p.Gln571His) | |
7 | g.17339584G>A | CA366895126 | AHR | c.1759G>A (p.Asp587Asn) c.1729G>A (p.Asp577Asn) c.1714G>A (p.Asp572Asn) | |
7 | g.17339584G>C | CA366895127 | AHR | c.1759G>C (p.Asp587His) c.1729G>C (p.Asp577His) c.1714G>C (p.Asp572His) | |
7 | g.17339584G>T | CA366895128 | AHR | c.1759G>T (p.Asp587Tyr) c.1729G>T (p.Asp577Tyr) c.1714G>T (p.Asp572Tyr) | |
7 | g.17339585A>C | CA366895129 | AHR | c.1760A>C (p.Asp587Ala) c.1730A>C (p.Asp577Ala) c.1715A>C (p.Asp572Ala) | |
7 | g.17339585A>G | CA366895130 | AHR | c.1760A>G (p.Asp587Gly) c.1730A>G (p.Asp577Gly) c.1715A>G (p.Asp572Gly) | |
7 | g.17339585A>T | CA366895131 | AHR | c.1760A>T (p.Asp587Val) c.1730A>T (p.Asp577Val) c.1715A>T (p.Asp572Val) | |
7 | g.17339586T>A | CA366895132 | AHR | c.1761T>A (p.Asp587Glu) c.1731T>A (p.Asp577Glu) c.1716T>A (p.Asp572Glu) | |
7 | g.17339586T>C | CA454134158 | AHR | c.1761T>C (p.Asp587=) c.1731T>C (p.Asp577=) c.1716T>C (p.Asp572=) | dbSNP |
7 | g.17339586T>G | CA366895133 | AHR | c.1761T>G (p.Asp587Glu) c.1731T>G (p.Asp577Glu) c.1716T>G (p.Asp572Glu) | |
7 | g.17339586T= | CA1691323888 | AHR | c.1761T= (p.Asp587=) c.1731T= (p.Asp577=) c.1716T= (p.Asp572=) | |
7 | g.17339587T>A | CA366895134 | AHR | c.1762T>A (p.Ser588Thr) c.1732T>A (p.Ser578Thr) c.1717T>A (p.Ser573Thr) | |
7 | g.17339587T>C | CA366895136 | AHR | c.1762T>C (p.Ser588Pro) c.1732T>C (p.Ser578Pro) c.1717T>C (p.Ser573Pro) | |
7 | g.17339587T>G | CA366895135 | AHR | c.1762T>G (p.Ser588Ala) c.1732T>G (p.Ser578Ala) c.1717T>G (p.Ser573Ala) | |
7 | g.17339588C>A | CA366895137 | AHR | c.1763C>A (p.Ser588Tyr) c.1733C>A (p.Ser578Tyr) c.1718C>A (p.Ser573Tyr) | gnomAD v4 |
7 | g.17339588C= | CA1691323889 | AHR | c.1763C= (p.Ser588=) c.1733C= (p.Ser578=) c.1718C= (p.Ser573=) | |
7 | g.17339588C>G | CA4172179 | AHR | c.1763C>G (p.Ser588Cys) c.1733C>G (p.Ser578Cys) c.1718C>G (p.Ser573Cys) | dbSNP ExAC gnomAD v2 |
7 | g.17339588C>T | CA366895138 | AHR | c.1763C>T (p.Ser588Phe) c.1733C>T (p.Ser578Phe) c.1718C>T (p.Ser573Phe) | |
7 | g.17339589T>A | CA454134159 | AHR | c.1764T>A (p.Ser588=) c.1734T>A (p.Ser578=) c.1719T>A (p.Ser573=) | |
7 | g.17339589T>C | CA454134161 | AHR | c.1764T>C (p.Ser588=) c.1734T>C (p.Ser578=) c.1719T>C (p.Ser573=) | |
7 | g.17339589T>G | CA454134160 | AHR | c.1764T>G (p.Ser588=) c.1734T>G (p.Ser578=) c.1719T>G (p.Ser573=) | |
7 | g.17339590T>A | CA366895139 | AHR | c.1765T>A (p.Leu589Ile) c.1735T>A (p.Leu579Ile) c.1720T>A (p.Leu574Ile) | |
7 | g.17339590T>C | CA454134162 | AHR | c.1765T>C (p.Leu589=) c.1735T>C (p.Leu579=) c.1720T>C (p.Leu574=) | |
7 | g.17339590T>G | CA366895140 | AHR | c.1765T>G (p.Leu589Val) c.1735T>G (p.Leu579Val) c.1720T>G (p.Leu574Val) | gnomAD v4 |
7 | g.17339590_17339594delinsTTAAG | CA1691323890 | AHR | c.1765_1769delinsTTAAG (p.Leu589=) c.1735_1739delinsTTAAG (p.Leu579=) c.1720_1724delinsTTAAG (p.Leu574=) | |
7 | g.17339591T>A | CA366895141 | AHR | c.1766T>A (p.Leu589Ter) c.1736T>A (p.Leu579Ter) c.1721T>A (p.Leu574Ter) | |
7 | g.17339591T>C | CA366895142 | AHR | c.1766T>C (p.Leu589Ser) c.1736T>C (p.Leu579Ser) c.1721T>C (p.Leu574Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.17339591T>G | CA366895143 | AHR | c.1766T>G (p.Leu589Ter) c.1736T>G (p.Leu579Ter) c.1721T>G (p.Leu574Ter) | gnomAD v4 |
7 | g.17339591T= | CA1691323891 | AHR | c.1766T= (p.Leu589=) c.1736T= (p.Leu579=) c.1721T= (p.Leu574=) | |
7 | g.17339596_17339599del | CA1098901327 | AHR | c.1771_1774del (p.Lys591LeufsTer16) c.1741_1744del (p.Lys581LeufsTer16) c.1726_1729del (p.Lys576LeufsTer16) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.17339592A>C | CA366895144 | AHR | c.1767A>C (p.Leu589Phe) c.1737A>C (p.Leu579Phe) c.1722A>C (p.Leu574Phe) | |
7 | g.17339592A>G | CA454134163 | AHR | c.1767A>G (p.Leu589=) c.1737A>G (p.Leu579=) c.1722A>G (p.Leu574=) | |
7 | g.17339592A>T | CA366895145 | AHR | c.1767A>T (p.Leu589Phe) c.1737A>T (p.Leu579Phe) c.1722A>T (p.Leu574Phe) | |
7 | g.17339593A= | CA1691323892 | AHR | c.1768A= (p.Ser590=) c.1738A= (p.Ser580=) c.1723A= (p.Ser575=) | |
7 | g.17339593A>C | CA366895148 | AHR | c.1768A>C (p.Ser590Arg) c.1738A>C (p.Ser580Arg) c.1723A>C (p.Ser575Arg) | dbSNP gnomAD v4 |
7 | g.17339593A>G | CA366895147 | AHR | c.1768A>G (p.Ser590Gly) c.1738A>G (p.Ser580Gly) c.1723A>G (p.Ser575Gly) | |
7 | g.17339593A>T | CA366895146 | AHR | c.1768A>T (p.Ser590Cys) c.1738A>T (p.Ser580Cys) c.1723A>T (p.Ser575Cys) | |
7 | g.17339594G>A | CA366895149 | AHR | c.1769G>A (p.Ser590Asn) c.1739G>A (p.Ser580Asn) c.1724G>A (p.Ser575Asn) | dbSNP gnomAD v2 |
7 | g.17339594G>C | CA366895150 | AHR | c.1769G>C (p.Ser590Thr) c.1739G>C (p.Ser580Thr) c.1724G>C (p.Ser575Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.17339594G= | CA1691323893 | AHR | c.1769G= (p.Ser590=) c.1739G= (p.Ser580=) c.1724G= (p.Ser575=) | |
7 | g.17339594G>T | CA366895151 | AHR | c.1769G>T (p.Ser590Ile) c.1739G>T (p.Ser580Ile) c.1724G>T (p.Ser575Ile) | |
7 | g.17339595T>A | CA366895152 | AHR | c.1770T>A (p.Ser590Arg) c.1740T>A (p.Ser580Arg) c.1725T>A (p.Ser575Arg) | |
7 | g.17339595T>C | CA454134164 | AHR | c.1770T>C (p.Ser590=) c.1740T>C (p.Ser580=) c.1725T>C (p.Ser575=) | |
7 | g.17339595T>G | CA366895153 | AHR | c.1770T>G (p.Ser590Arg) c.1740T>G (p.Ser580Arg) c.1725T>G (p.Ser575Arg) | |
7 | g.17339596A>C | CA366895154 | AHR | c.1771A>C (p.Lys591Gln) c.1741A>C (p.Lys581Gln) c.1726A>C (p.Lys576Gln) | |
7 | g.17339596A>G | CA366895155 | AHR | c.1771A>G (p.Lys591Glu) c.1741A>G (p.Lys581Glu) c.1726A>G (p.Lys576Glu) | gnomAD v4 |
7 | g.17339596A>T | CA366895156 | AHR | c.1771A>T (p.Lys591Ter) c.1741A>T (p.Lys581Ter) c.1726A>T (p.Lys576Ter) | |
7 | g.17339597A>C | CA366895157 | AHR | c.1772A>C (p.Lys591Thr) c.1742A>C (p.Lys581Thr) c.1727A>C (p.Lys576Thr) | |
7 | g.17339597A>G | CA366895158 | AHR | c.1772A>G (p.Lys591Arg) c.1742A>G (p.Lys581Arg) c.1727A>G (p.Lys576Arg) | |
7 | g.17339597A>T | CA366895159 | AHR | c.1772A>T (p.Lys591Met) c.1742A>T (p.Lys581Met) c.1727A>T (p.Lys576Met) | gnomAD v4 |
7 | g.17339598G>A | CA454134165 | AHR | c.1773G>A (p.Lys591=) c.1743G>A (p.Lys581=) c.1728G>A (p.Lys576=) | |
7 | g.17339598G>C | CA366895160 | AHR | c.1773G>C (p.Lys591Asn) c.1743G>C (p.Lys581Asn) c.1728G>C (p.Lys576Asn) | gnomAD v4 |
7 | g.17339598G>T | CA366895161 | AHR | c.1773G>T (p.Lys591Asn) c.1743G>T (p.Lys581Asn) c.1728G>T (p.Lys576Asn) | |
7 | g.17339599T>A | CA366895164 | AHR | c.1774T>A (p.Ser592Thr) c.1744T>A (p.Ser582Thr) c.1729T>A (p.Ser577Thr) | |
7 | g.17339599T>C | CA366895162 | AHR | c.1774T>C (p.Ser592Pro) c.1744T>C (p.Ser582Pro) c.1729T>C (p.Ser577Pro) | |
7 | g.17339599T>G | CA366895163 | AHR | c.1774T>G (p.Ser592Ala) c.1744T>G (p.Ser582Ala) c.1729T>G (p.Ser577Ala) | |
7 | g.17339600C>A | CA366895165 | AHR | c.1775C>A (p.Ser592Tyr) c.1745C>A (p.Ser582Tyr) c.1730C>A (p.Ser577Tyr) | |
7 | g.17339600C= | CA1691323894 | AHR | c.1775C= (p.Ser592=) c.1745C= (p.Ser582=) c.1730C= (p.Ser577=) | |
7 | g.17339600C>G | CA4172180 | AHR | c.1775C>G (p.Ser592Cys) c.1745C>G (p.Ser582Cys) c.1730C>G (p.Ser577Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.17339600C>T | CA366895166 | AHR | c.1775C>T (p.Ser592Phe) c.1745C>T (p.Ser582Phe) c.1730C>T (p.Ser577Phe) | gnomAD v4 |
7 | g.17339601T>A | CA454134166 | AHR | c.1776T>A (p.Ser592=) c.1746T>A (p.Ser582=) c.1731T>A (p.Ser577=) | |
7 | g.17339601T>C | CA454134167 | AHR | c.1776T>C (p.Ser592=) c.1746T>C (p.Ser582=) c.1731T>C (p.Ser577=) | |
7 | g.17339601T>G | CA454134168 | AHR | c.1776T>G (p.Ser592=) c.1746T>G (p.Ser582=) c.1731T>G (p.Ser577=) | |
7 | g.17339602C>A | CA366895167 | AHR | c.1777C>A (p.Pro593Thr) c.1747C>A (p.Pro583Thr) c.1732C>A (p.Pro578Thr) | |
7 | g.17339602C= | CA1691323895 | AHR | c.1777C= (p.Pro593=) c.1747C= (p.Pro583=) c.1732C= (p.Pro578=) | |
7 | g.17339602C>G | CA4172181 | AHR | c.1777C>G (p.Pro593Ala) c.1747C>G (p.Pro583Ala) c.1732C>G (p.Pro578Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.17339602C>T | CA366895168 | AHR | c.1777C>T (p.Pro593Ser) c.1747C>T (p.Pro583Ser) c.1732C>T (p.Pro578Ser) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.17339603C>A | CA366895169 | AHR | c.1778C>A (p.Pro593His) c.1748C>A (p.Pro583His) c.1733C>A (p.Pro578His) | |
7 | g.17339603C>G | CA366895170 | AHR | c.1778C>G (p.Pro593Arg) c.1748C>G (p.Pro583Arg) c.1733C>G (p.Pro578Arg) | |
7 | g.17339603C>T | CA366895171 | AHR | c.1778C>T (p.Pro593Leu) c.1748C>T (p.Pro583Leu) c.1733C>T (p.Pro578Leu) | |
7 | g.17339604C>A | CA454134171 | AHR | c.1779C>A (p.Pro593=) c.1749C>A (p.Pro583=) c.1734C>A (p.Pro578=) | |
7 | g.17339604C>G | CA454134169 | AHR | c.1779C>G (p.Pro593=) c.1749C>G (p.Pro583=) c.1734C>G (p.Pro578=) | |
7 | g.17339604C>T | CA454134170 | AHR | c.1779C>T (p.Pro593=) c.1749C>T (p.Pro583=) c.1734C>T (p.Pro578=) | |
7 | g.17339605T>A | CA366895172 | AHR | c.1780T>A (p.Phe594Ile) c.1750T>A (p.Phe584Ile) c.1735T>A (p.Phe579Ile) | |
7 | g.17339605T>C | CA366895173 | AHR | c.1780T>C (p.Phe594Leu) c.1750T>C (p.Phe584Leu) c.1735T>C (p.Phe579Leu) | dbSNP |
7 | g.17339605T>G | CA366895174 | AHR | c.1780T>G (p.Phe594Val) c.1750T>G (p.Phe584Val) c.1735T>G (p.Phe579Val) | |
7 | g.17339605T= | CA1691323896 | AHR | c.1780T= (p.Phe594=) c.1750T= (p.Phe584=) c.1735T= (p.Phe579=) | |
7 | g.17339606del | CA2681909912 | AHR | c.1781del (p.Phe594SerfsTer14) c.1751del (p.Phe584SerfsTer14) c.1736del (p.Phe579SerfsTer14) | gnomAD v4 |
7 | g.17339606T>A | CA366895176 | AHR | c.1781T>A (p.Phe594Tyr) c.1751T>A (p.Phe584Tyr) c.1736T>A (p.Phe579Tyr) | |
7 | g.17339606T>C | CA366895177 | AHR | c.1781T>C (p.Phe594Ser) c.1751T>C (p.Phe584Ser) c.1736T>C (p.Phe579Ser) | |
7 | g.17339606T>G | CA366895175 | AHR | c.1781T>G (p.Phe594Cys) c.1751T>G (p.Phe584Cys) c.1736T>G (p.Phe579Cys) | |
7 | g.17339607C>A | CA366895178 | AHR | c.1782C>A (p.Phe594Leu) c.1752C>A (p.Phe584Leu) c.1737C>A (p.Phe579Leu) | gnomAD v4 |
7 | g.17339607C>G | CA366895179 | AHR | c.1782C>G (p.Phe594Leu) c.1752C>G (p.Phe584Leu) c.1737C>G (p.Phe579Leu) | |
7 | g.17339607C>T | CA454134172 | AHR | c.1782C>T (p.Phe594=) c.1752C>T (p.Phe584=) c.1737C>T (p.Phe579=) | |
7 | g.17339608A= | CA1691323897 | AHR | c.1783A= (p.Ile595=) c.1753A= (p.Ile585=) c.1738A= (p.Ile580=) | |
7 | g.17339608A>C | CA366895180 | AHR | c.1783A>C (p.Ile595Leu) c.1753A>C (p.Ile585Leu) c.1738A>C (p.Ile580Leu) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.17339608A>G | CA366895181 | AHR | c.1783A>G (p.Ile595Val) c.1753A>G (p.Ile585Val) c.1738A>G (p.Ile580Val) | |
7 | g.17339608A>T | CA366895182 | AHR | c.1783A>T (p.Ile595Leu) c.1753A>T (p.Ile585Leu) c.1738A>T (p.Ile580Leu) | |
7 | g.17339609T>A | CA366895183 | AHR | c.1784T>A (p.Ile595Lys) c.1754T>A (p.Ile585Lys) c.1739T>A (p.Ile580Lys) | |
7 | g.17339609T>C | CA366895184 | AHR | c.1784T>C (p.Ile595Thr) c.1754T>C (p.Ile585Thr) c.1739T>C (p.Ile580Thr) | |
7 | g.17339609T>G | CA366895185 | AHR | c.1784T>G (p.Ile595Arg) c.1754T>G (p.Ile585Arg) c.1739T>G (p.Ile580Arg) | |
7 | g.17339610A>C | CA454134173 | AHR | c.1785A>C (p.Ile595=) c.1755A>C (p.Ile585=) c.1740A>C (p.Ile580=) | |
7 | g.17339610A>G | CA366895186 | AHR | c.1785A>G (p.Ile595Met) c.1755A>G (p.Ile585Met) c.1740A>G (p.Ile580Met) | |
7 | g.17339610A>T | CA454134174 | AHR | c.1785A>T (p.Ile595=) c.1755A>T (p.Ile585=) c.1740A>T (p.Ile580=) | |
7 | g.17339611C>A | CA366895187 | AHR | c.1786C>A (p.Pro596Thr) c.1756C>A (p.Pro586Thr) c.1741C>A (p.Pro581Thr) | |
7 | g.17339611C= | CA1691323898 | AHR | c.1786C= (p.Pro596=) c.1756C= (p.Pro586=) c.1741C= (p.Pro581=) | |
7 | g.17339611C>G | CA366895188 | AHR | c.1786C>G (p.Pro596Ala) c.1756C>G (p.Pro586Ala) c.1741C>G (p.Pro581Ala) | |
7 | g.17339611C>T | CA366895189 | AHR | c.1786C>T (p.Pro596Ser) c.1756C>T (p.Pro586Ser) c.1741C>T (p.Pro581Ser) | dbSNP gnomAD v4 |
7 | g.17339612C>A | CA366895190 | AHR | c.1787C>A (p.Pro596His) c.1757C>A (p.Pro586His) c.1742C>A (p.Pro581His) | |
7 | g.17339612C>G | CA366895191 | AHR | c.1787C>G (p.Pro596Arg) c.1757C>G (p.Pro586Arg) c.1742C>G (p.Pro581Arg) | |
7 | g.17339612C>T | CA366895192 | AHR | c.1787C>T (p.Pro596Leu) c.1757C>T (p.Pro586Leu) c.1742C>T (p.Pro581Leu) | |
7 | g.17339613T>A | CA454134175 | AHR | c.1788T>A (p.Pro596=) c.1758T>A (p.Pro586=) c.1743T>A (p.Pro581=) | |
7 | g.17339613T>C | CA454134176 | AHR | c.1788T>C (p.Pro596=) c.1758T>C (p.Pro586=) c.1743T>C (p.Pro581=) | |
7 | g.17339613T>G | CA454134177 | AHR | c.1788T>G (p.Pro596=) c.1758T>G (p.Pro586=) c.1743T>G (p.Pro581=) | |
7 | g.17339614T>A | CA366895195 | AHR | c.1789T>A (p.Ser597Thr) c.1759T>A (p.Ser587Thr) c.1744T>A (p.Ser582Thr) | |
7 | g.17339614T>C | CA366895193 | AHR | c.1789T>C (p.Ser597Pro) c.1759T>C (p.Ser587Pro) c.1744T>C (p.Ser582Pro) | |
7 | g.17339614T>G | CA366895194 | AHR | c.1789T>G (p.Ser597Ala) c.1759T>G (p.Ser587Ala) c.1744T>G (p.Ser582Ala) | gnomAD v4 |
7 | g.17339615C>A | CA366895196 | AHR | c.1790C>A (p.Ser597Ter) c.1760C>A (p.Ser587Ter) c.1745C>A (p.Ser582Ter) | |
7 | g.17339615C= | CA1691323899 | AHR | c.1790C= (p.Ser597=) c.1760C= (p.Ser587=) c.1745C= (p.Ser582=) | |
7 | g.17339615C>G | CA366895197 | AHR | c.1790C>G (p.Ser597Ter) c.1760C>G (p.Ser587Ter) c.1745C>G (p.Ser582Ter) | COSMIC |
7 | g.17339615C>T | CA366895198 | AHR | c.1790C>T (p.Ser597Leu) c.1760C>T (p.Ser587Leu) c.1745C>T (p.Ser582Leu) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.17339616A= | CA1691323900 | AHR | c.1791A= (p.Ser597=) c.1761A= (p.Ser587=) c.1746A= (p.Ser582=) | |
7 | g.17339616A>C | CA454134178 | AHR | c.1791A>C (p.Ser597=) c.1761A>C (p.Ser587=) c.1746A>C (p.Ser582=) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.17339616A>G | CA154120882 | AHR | c.1791A>G (p.Ser597=) c.1761A>G (p.Ser587=) c.1746A>G (p.Ser582=) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.17339616A>T | CA4172182 | AHR | c.1791A>T (p.Ser597=) c.1761A>T (p.Ser587=) c.1746A>T (p.Ser582=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.17339617G>A | CA366895199 | AHR | c.1792G>A (p.Asp598Asn) c.1762G>A (p.Asp588Asn) c.1747G>A (p.Asp583Asn) | |
7 | g.17339617G>C | CA366895200 | AHR | c.1792G>C (p.Asp598His) c.1762G>C (p.Asp588His) c.1747G>C (p.Asp583His) | |
7 | g.17339617G>T | CA366895201 | AHR | c.1792G>T (p.Asp598Tyr) c.1762G>T (p.Asp588Tyr) c.1747G>T (p.Asp583Tyr) | |
7 | g.17339618A= | CA1691323901 | AHR | c.1793A= (p.Asp598=) c.1763A= (p.Asp588=) c.1748A= (p.Asp583=) | |
7 | g.17339618A>C | CA366895202 | AHR | c.1793A>C (p.Asp598Ala) c.1763A>C (p.Asp588Ala) c.1748A>C (p.Asp583Ala) | |
7 | g.17339618A>G | CA4172183 | AHR | c.1793A>G (p.Asp598Gly) c.1763A>G (p.Asp588Gly) c.1748A>G (p.Asp583Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.17339618A>T | CA366895203 | AHR | c.1793A>T (p.Asp598Val) c.1763A>T (p.Asp588Val) c.1748A>T (p.Asp583Val) | |
7 | g.17339619T>A | CA366895204 | AHR | c.1794T>A (p.Asp598Glu) c.1764T>A (p.Asp588Glu) c.1749T>A (p.Asp583Glu) | |
7 | g.17339619T>C | CA454134179 | AHR | c.1794T>C (p.Asp598=) c.1764T>C (p.Asp588=) c.1749T>C (p.Asp583=) | |
7 | g.17339619T>G | CA366895205 | AHR | c.1794T>G (p.Asp598Glu) c.1764T>G (p.Asp588Glu) c.1749T>G (p.Asp583Glu) | |
7 | g.17339620T>A | CA366895206 | AHR | c.1795T>A (p.Tyr599Asn) c.1765T>A (p.Tyr589Asn) c.1750T>A (p.Tyr584Asn) | |
7 | g.17339620T>C | CA366895208 | AHR | c.1795T>C (p.Tyr599His) c.1765T>C (p.Tyr589His) c.1750T>C (p.Tyr584His) | |
7 | g.17339620T>G | CA366895207 | AHR | c.1795T>G (p.Tyr599Asp) c.1765T>G (p.Tyr589Asp) c.1750T>G (p.Tyr584Asp) | |
7 | g.17339621A= | CA1691323902 | AHR | c.1796A= (p.Tyr599=) c.1766A= (p.Tyr589=) c.1751A= (p.Tyr584=) | |
7 | g.17339621A>C | CA366895209 | AHR | c.1796A>C (p.Tyr599Ser) c.1766A>C (p.Tyr589Ser) c.1751A>C (p.Tyr584Ser) | |
7 | g.17339621A>G | CA4172184 | AHR | c.1796A>G (p.Tyr599Cys) c.1766A>G (p.Tyr589Cys) c.1751A>G (p.Tyr584Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.17339621A>T | CA366895210 | AHR | c.1796A>T (p.Tyr599Phe) c.1766A>T (p.Tyr589Phe) c.1751A>T (p.Tyr584Phe) | |
7 | g.17339622T>A | CA366895211 | AHR | c.1797T>A (p.Tyr599Ter) c.1767T>A (p.Tyr589Ter) c.1752T>A (p.Tyr584Ter) | |
7 | g.17339622T>C | CA454134180 | AHR | c.1797T>C (p.Tyr599=) c.1767T>C (p.Tyr589=) c.1752T>C (p.Tyr584=) | |
7 | g.17339622T>G | CA366895212 | AHR | c.1797T>G (p.Tyr599Ter) c.1767T>G (p.Tyr589Ter) c.1752T>G (p.Tyr584Ter) | |
7 | g.17339623C>A | CA366895213 | AHR | c.1798C>A (p.Gln600Lys) c.1768C>A (p.Gln590Lys) c.1753C>A (p.Gln585Lys) | |
7 | g.17339623C>G | CA366895214 | AHR | c.1798C>G (p.Gln600Glu) c.1768C>G (p.Gln590Glu) c.1753C>G (p.Gln585Glu) | |
7 | g.17339623C>T | CA366895215 | AHR | c.1798C>T (p.Gln600Ter) c.1768C>T (p.Gln590Ter) c.1753C>T (p.Gln585Ter) | |
7 | g.17339624A>C | CA366895216 | AHR | c.1799A>C (p.Gln600Pro) c.1769A>C (p.Gln590Pro) c.1754A>C (p.Gln585Pro) | |
7 | g.17339624A>G | CA366895217 | AHR | c.1799A>G (p.Gln600Arg) c.1769A>G (p.Gln590Arg) c.1754A>G (p.Gln585Arg) | |
7 | g.17339624A>T | CA366895218 | AHR | c.1799A>T (p.Gln600Leu) c.1769A>T (p.Gln590Leu) c.1754A>T (p.Gln585Leu) | |
7 | g.17339625A= | CA1691323903 | AHR | c.1800A= (p.Gln600=) c.1770A= (p.Gln590=) c.1755A= (p.Gln585=) | |
7 | g.17339625A>C | CA366895220 | AHR | c.1800A>C (p.Gln600His) c.1770A>C (p.Gln590His) c.1755A>C (p.Gln585His) | gnomAD v4 |
7 | g.17339625A>G | CA4172185 | AHR | c.1800A>G (p.Gln600=) c.1770A>G (p.Gln590=) c.1755A>G (p.Gln585=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.17339625A>T | CA366895219 | AHR | c.1800A>T (p.Gln600His) c.1770A>T (p.Gln590His) c.1755A>T (p.Gln585His) | |
7 | g.17339626C>A | CA366895221 | AHR | c.1801C>A (p.Gln601Lys) c.1771C>A (p.Gln591Lys) c.1756C>A (p.Gln586Lys) | |
7 | g.17339626C= | CA1691323904 | AHR | c.1801C= (p.Gln601=) c.1771C= (p.Gln591=) c.1756C= (p.Gln586=) | |
7 | g.17339626C>G | CA366895222 | AHR | c.1801C>G (p.Gln601Glu) c.1771C>G (p.Gln591Glu) c.1756C>G (p.Gln586Glu) | |
7 | g.17339626C>T | CA154120903 | AHR | c.1801C>T (p.Gln601Ter) c.1771C>T (p.Gln591Ter) c.1756C>T (p.Gln586Ter) | dbSNP |
7 | g.17339627A= | CA1691323905 | AHR | c.1802A= (p.Gln601=) c.1772A= (p.Gln591=) c.1757A= (p.Gln586=) | |
7 | g.17339627A>C | CA366895223 | AHR | c.1802A>C (p.Gln601Pro) c.1772A>C (p.Gln591Pro) c.1757A>C (p.Gln586Pro) | |
7 | g.17339627A>G | CA366895224 | AHR | c.1802A>G (p.Gln601Arg) c.1772A>G (p.Gln591Arg) c.1757A>G (p.Gln586Arg) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.17339627A>T | CA366895225 | AHR | c.1802A>T (p.Gln601Leu) c.1772A>T (p.Gln591Leu) c.1757A>T (p.Gln586Leu) | |
7 | g.17339628G>A | CA154120917 | AHR | c.1803G>A (p.Gln601=) c.1773G>A (p.Gln591=) c.1758G>A (p.Gln586=) | dbSNP |
7 | g.17339628G>C | CA366895226 | AHR | c.1803G>C (p.Gln601His) c.1773G>C (p.Gln591His) c.1758G>C (p.Gln586His) | |
7 | g.17339628G= | CA1691323906 | AHR | c.1803G= (p.Gln601=) c.1773G= (p.Gln591=) c.1758G= (p.Gln586=) | |
7 | g.17339628G>T | CA366895227 | AHR | c.1803G>T (p.Gln601His) c.1773G>T (p.Gln591His) c.1758G>T (p.Gln586His) |