UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.17339491A= | CA1691323854 | AHR | c.1666A= (p.Met556=) c.1636A= (p.Met546=) c.1621A= (p.Met541=) n.648A= | |
| 7 | g.17339491A>C | CA154120752 | AHR | c.1666A>C (p.Met556Leu) c.1636A>C (p.Met546Leu) c.1621A>C (p.Met541Leu) n.648A>C | dbSNP |
| 7 | g.17339491A>G | CA366894906 | AHR | c.1666A>G (p.Met556Val) c.1636A>G (p.Met546Val) c.1621A>G (p.Met541Val) n.648A>G | dbSNP gnomAD v4 |
| 7 | g.17339491A>T | CA366894908 | AHR | c.1666A>T (p.Met556Leu) c.1636A>T (p.Met546Leu) c.1621A>T (p.Met541Leu) n.648A>T | |
| 7 | g.17339492T>A | CA366894910 | AHR | c.1667T>A (p.Met556Lys) c.1637T>A (p.Met546Lys) c.1622T>A (p.Met541Lys) n.649T>A | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.17339492T>C | CA366894912 | AHR | c.1667T>C (p.Met556Thr) c.1637T>C (p.Met546Thr) c.1622T>C (p.Met541Thr) n.649T>C | gnomAD v4 |
| 7 | g.17339492T>G | CA366894913 | AHR | c.1667T>G (p.Met556Arg) c.1637T>G (p.Met546Arg) c.1622T>G (p.Met541Arg) n.649T>G | |
| 7 | g.17339492T= | CA1691323855 | AHR | c.1667T= (p.Met556=) c.1637T= (p.Met546=) c.1622T= (p.Met541=) n.649T= | |
| 7 | g.17339493G>A | CA366894914 | AHR | c.1668G>A (p.Met556Ile) c.1638G>A (p.Met546Ile) c.1623G>A (p.Met541Ile) n.650G>A | |
| 7 | g.17339493G>C | CA366894915 | AHR | c.1668G>C (p.Met556Ile) c.1638G>C (p.Met546Ile) c.1623G>C (p.Met541Ile) n.650G>C | |
| 7 | g.17339493G>T | CA366894916 | AHR | c.1668G>T (p.Met556Ile) c.1638G>T (p.Met546Ile) c.1623G>T (p.Met541Ile) n.650G>T | gnomAD v4 COSMIC |
| 7 | g.17339494C>A | CA366894917 | AHR | c.1669C>A (p.Gln557Lys) c.1639C>A (p.Gln547Lys) c.1624C>A (p.Gln542Lys) n.651C>A | |
| 7 | g.17339494C>G | CA366894918 | AHR | c.1669C>G (p.Gln557Glu) c.1639C>G (p.Gln547Glu) c.1624C>G (p.Gln542Glu) n.651C>G | |
| 7 | g.17339494C>T | CA366894919 | AHR | c.1669C>T (p.Gln557Ter) c.1639C>T (p.Gln547Ter) c.1624C>T (p.Gln542Ter) n.651C>T | |
| 7 | g.17339495A>C | CA366894921 | AHR | c.1670A>C (p.Gln557Pro) c.1640A>C (p.Gln547Pro) c.1625A>C (p.Gln542Pro) n.652A>C | |
| 7 | g.17339495A>G | CA366894922 | AHR | c.1670A>G (p.Gln557Arg) c.1640A>G (p.Gln547Arg) c.1625A>G (p.Gln542Arg) n.652A>G | |
| 7 | g.17339495A>T | CA366894920 | AHR | c.1670A>T (p.Gln557Leu) c.1640A>T (p.Gln547Leu) c.1625A>T (p.Gln542Leu) n.652A>T | |
| 7 | g.17339496G>A | CA454134115 | AHR | c.1671G>A (p.Gln557=) c.1641G>A (p.Gln547=) c.1626G>A (p.Gln542=) n.653G>A | |
| 7 | g.17339496G>C | CA366894923 | AHR | c.1671G>C (p.Gln557His) c.1641G>C (p.Gln547His) c.1626G>C (p.Gln542His) n.653G>C | gnomAD v4 |
| 7 | g.17339496G>T | CA366894924 | AHR | c.1671G>T (p.Gln557His) c.1641G>T (p.Gln547His) c.1626G>T (p.Gln542His) n.653G>T | |
| 7 | g.17339497A>C | CA366894925 | AHR | c.1672A>C (p.Asn558His) c.1642A>C (p.Asn548His) c.1627A>C (p.Asn543His) n.654A>C | |
| 7 | g.17339497A>G | CA366894926 | AHR | c.1672A>G (p.Asn558Asp) c.1642A>G (p.Asn548Asp) c.1627A>G (p.Asn543Asp) n.654A>G | |
| 7 | g.17339497A>T | CA366894927 | AHR | c.1672A>T (p.Asn558Tyr) c.1642A>T (p.Asn548Tyr) c.1627A>T (p.Asn543Tyr) n.654A>T | |
| 7 | g.17339498A= | CA1691323856 | AHR | c.1673A= (p.Asn558=) c.1643A= (p.Asn548=) c.1628A= (p.Asn543=) n.655A= | |
| 7 | g.17339498A>C | CA154120753 | AHR | c.1673A>C (p.Asn558Thr) c.1643A>C (p.Asn548Thr) c.1628A>C (p.Asn543Thr) n.655A>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.17339498A>G | CA366894928 | AHR | c.1673A>G (p.Asn558Ser) c.1643A>G (p.Asn548Ser) c.1628A>G (p.Asn543Ser) n.655A>G | |
| 7 | g.17339498A>T | CA366894929 | AHR | c.1673A>T (p.Asn558Ile) c.1643A>T (p.Asn548Ile) c.1628A>T (p.Asn543Ile) n.655A>T | |
| 7 | g.17339499T>A | CA366894930 | AHR | c.1674T>A (p.Asn558Lys) c.1644T>A (p.Asn548Lys) c.1629T>A (p.Asn543Lys) n.656T>A | |
| 7 | g.17339499T>C | CA454134116 | AHR | c.1674T>C (p.Asn558=) c.1644T>C (p.Asn548=) c.1629T>C (p.Asn543=) n.656T>C | |
| 7 | g.17339499T>G | CA366894931 | AHR | c.1674T>G (p.Asn558Lys) c.1644T>G (p.Asn548Lys) c.1629T>G (p.Asn543Lys) n.656T>G | gnomAD v4 |
| 7 | g.17339500G>A | CA366894932 | AHR | c.1675G>A (p.Glu559Lys) c.1645G>A (p.Glu549Lys) c.1630G>A (p.Glu544Lys) n.657G>A | |
| 7 | g.17339500G>C | CA366894933 | AHR | c.1675G>C (p.Glu559Gln) c.1645G>C (p.Glu549Gln) c.1630G>C (p.Glu544Gln) n.657G>C | |
| 7 | g.17339500G>T | CA366894934 | AHR | c.1675G>T (p.Glu559Ter) c.1645G>T (p.Glu549Ter) c.1630G>T (p.Glu544Ter) n.657G>T | |
| 7 | g.17339501A>C | CA366894937 | AHR | c.1676A>C (p.Glu559Ala) c.1646A>C (p.Glu549Ala) c.1631A>C (p.Glu544Ala) n.658A>C | |
| 7 | g.17339501A>G | CA366894935 | AHR | c.1676A>G (p.Glu559Gly) c.1646A>G (p.Glu549Gly) c.1631A>G (p.Glu544Gly) n.658A>G | |
| 7 | g.17339501A>T | CA366894936 | AHR | c.1676A>T (p.Glu559Val) c.1646A>T (p.Glu549Val) c.1631A>T (p.Glu544Val) n.658A>T | |
| 7 | g.17339502A>C | CA366894938 | AHR | c.1677A>C (p.Glu559Asp) c.1647A>C (p.Glu549Asp) c.1632A>C (p.Glu544Asp) n.659A>C | |
| 7 | g.17339502A>G | CA454134117 | AHR | c.1677A>G (p.Glu559=) c.1647A>G (p.Glu549=) c.1632A>G (p.Glu544=) n.659A>G | gnomAD v4 |
| 7 | g.17339502A>T | CA366894939 | AHR | c.1677A>T (p.Glu559Asp) c.1647A>T (p.Glu549Asp) c.1632A>T (p.Glu544Asp) n.659A>T | |
| 7 | g.17339503A>C | CA366894940 | AHR | c.1678A>C (p.Lys560Gln) c.1648A>C (p.Lys550Gln) c.1633A>C (p.Lys545Gln) n.660A>C | |
| 7 | g.17339503A>G | CA366894942 | AHR | c.1678A>G (p.Lys560Glu) c.1648A>G (p.Lys550Glu) c.1633A>G (p.Lys545Glu) n.660A>G | |
| 7 | g.17339503A>T | CA366894941 | AHR | c.1678A>T (p.Lys560Ter) c.1648A>T (p.Lys550Ter) c.1633A>T (p.Lys545Ter) n.660A>T | |
| 7 | g.17339504A= | CA1691323857 | AHR | c.1679A= (p.Lys560=) c.1649A= (p.Lys550=) c.1634A= (p.Lys545=) n.661A= | |
| 7 | g.17339504A>C | CA366894943 | AHR | c.1679A>C (p.Lys560Thr) c.1649A>C (p.Lys550Thr) c.1634A>C (p.Lys545Thr) n.661A>C | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.17339504A>G | CA366894944 | AHR | c.1679A>G (p.Lys560Arg) c.1649A>G (p.Lys550Arg) c.1634A>G (p.Lys545Arg) n.661A>G | gnomAD v4 |
| 7 | g.17339504A>T | CA366894945 | AHR | c.1679A>T (p.Lys560Ile) c.1649A>T (p.Lys550Ile) c.1634A>T (p.Lys545Ile) n.661A>T | |
| 7 | g.17339505A>C | CA366894946 | AHR | c.1680A>C (p.Lys560Asn) c.1650A>C (p.Lys550Asn) c.1635A>C (p.Lys545Asn) n.662A>C | gnomAD v4 |
| 7 | g.17339505A>G | CA454134118 | AHR | c.1680A>G (p.Lys560=) c.1650A>G (p.Lys550=) c.1635A>G (p.Lys545=) n.662A>G | |
| 7 | g.17339505A>T | CA366894947 | AHR | c.1680A>T (p.Lys560Asn) c.1650A>T (p.Lys550Asn) c.1635A>T (p.Lys545Asn) n.662A>T | |
| 7 | g.17339506T>A | CA366894948 | AHR | c.1681T>A (p.Phe561Ile) c.1651T>A (p.Phe551Ile) c.1636T>A (p.Phe546Ile) n.663T>A | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.17339506T>C | CA366894949 | AHR | c.1681T>C (p.Phe561Leu) c.1651T>C (p.Phe551Leu) c.1636T>C (p.Phe546Leu) n.663T>C | |
| 7 | g.17339506T>G | CA366894950 | AHR | c.1681T>G (p.Phe561Val) c.1651T>G (p.Phe551Val) c.1636T>G (p.Phe546Val) n.663T>G | |
| 7 | g.17339506T= | CA1691323858 | AHR | c.1681T= (p.Phe561=) c.1651T= (p.Phe551=) c.1636T= (p.Phe546=) n.663T= | |
| 7 | g.17339510del | CA645548963 | AHR | c.1685del (p.Phe562SerfsTer16) c.1655del (p.Phe552SerfsTer16) c.1640del (p.Phe547SerfsTer16) n.667del | COSMIC |
| 7 | g.17339507T>A | CA366894951 | AHR | c.1682T>A (p.Phe561Tyr) c.1652T>A (p.Phe551Tyr) c.1637T>A (p.Phe546Tyr) n.664T>A | |
| 7 | g.17339507T>C | CA366894952 | AHR | c.1682T>C (p.Phe561Ser) c.1652T>C (p.Phe551Ser) c.1637T>C (p.Phe546Ser) n.664T>C | |
| 7 | g.17339507T>G | CA366894953 | AHR | c.1682T>G (p.Phe561Cys) c.1652T>G (p.Phe551Cys) c.1637T>G (p.Phe546Cys) n.664T>G | |
| 7 | g.17339508T>A | CA366894954 | AHR | c.1683T>A (p.Phe561Leu) c.1653T>A (p.Phe551Leu) c.1638T>A (p.Phe546Leu) n.665T>A | |
| 7 | g.17339508T>C | CA454134119 | AHR | c.1683T>C (p.Phe561=) c.1653T>C (p.Phe551=) c.1638T>C (p.Phe546=) n.665T>C | gnomAD v4 |
| 7 | g.17339508T>G | CA366894955 | AHR | c.1683T>G (p.Phe561Leu) c.1653T>G (p.Phe551Leu) c.1638T>G (p.Phe546Leu) n.665T>G | |
| 7 | g.17339509T>A | CA366894956 | AHR | c.1684T>A (p.Phe562Ile) c.1654T>A (p.Phe552Ile) c.1639T>A (p.Phe547Ile) n.666T>A | |
| 7 | g.17339509T>C | CA366894958 | AHR | c.1684T>C (p.Phe562Leu) c.1654T>C (p.Phe552Leu) c.1639T>C (p.Phe547Leu) n.666T>C | |
| 7 | g.17339509T>G | CA366894957 | AHR | c.1684T>G (p.Phe562Val) c.1654T>G (p.Phe552Val) c.1639T>G (p.Phe547Val) n.666T>G | gnomAD v4 |
| 7 | g.17339510T>A | CA366894959 | AHR | c.1685T>A (p.Phe562Tyr) c.1655T>A (p.Phe552Tyr) c.1640T>A (p.Phe547Tyr) n.667T>A | |
| 7 | g.17339510T>C | CA366894960 | AHR | c.1685T>C (p.Phe562Ser) c.1655T>C (p.Phe552Ser) c.1640T>C (p.Phe547Ser) n.667T>C | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.17339510T>G | CA366894961 | AHR | c.1685T>G (p.Phe562Cys) c.1655T>G (p.Phe552Cys) c.1640T>G (p.Phe547Cys) n.667T>G | |
| 7 | g.17339510T= | CA1691323859 | AHR | c.1685T= (p.Phe562=) c.1655T= (p.Phe552=) c.1640T= (p.Phe547=) n.667T= | |
| 7 | g.17339511C>A | CA366894962 | AHR | c.1686C>A (p.Phe562Leu) c.1656C>A (p.Phe552Leu) c.1641C>A (p.Phe547Leu) n.668C>A | |
| 7 | g.17339511C>G | CA366894963 | AHR | c.1686C>G (p.Phe562Leu) c.1656C>G (p.Phe552Leu) c.1641C>G (p.Phe547Leu) n.668C>G | |
| 7 | g.17339511C>T | CA454134120 | AHR | c.1686C>T (p.Phe562=) c.1656C>T (p.Phe552=) c.1641C>T (p.Phe547=) n.668C>T | |
| 7 | g.17339512A>C | CA454134121 | AHR | c.1687A>C (p.Arg563=) c.1657A>C (p.Arg553=) c.1642A>C (p.Arg548=) n.669A>C | |
| 7 | g.17339512A>G | CA366894964 | AHR | c.1687A>G (p.Arg563Gly) c.1657A>G (p.Arg553Gly) c.1642A>G (p.Arg548Gly) n.669A>G | |
| 7 | g.17339512A>T | CA366894965 | AHR | c.1687A>T (p.Arg563Ter) c.1657A>T (p.Arg553Ter) c.1642A>T (p.Arg548Ter) n.669A>T | |
| 7 | g.17339513G>A | CA366894966 | AHR | c.1688G>A (p.Arg563Lys) c.1658G>A (p.Arg553Lys) c.1643G>A (p.Arg548Lys) n.670G>A | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.17339513G>C | CA366894967 | AHR | c.1688G>C (p.Arg563Thr) c.1658G>C (p.Arg553Thr) c.1643G>C (p.Arg548Thr) n.670G>C | |
| 7 | g.17339513G= | CA1691323860 | AHR | c.1688G= (p.Arg563=) c.1658G= (p.Arg553=) c.1643G= (p.Arg548=) n.670G= | |
| 7 | g.17339513G>T | CA366894968 | AHR | c.1688G>T (p.Arg563Ile) c.1658G>T (p.Arg553Ile) c.1643G>T (p.Arg548Ile) n.670G>T | |
| 7 | g.17339514A= | CA1691323861 | AHR | c.1689A= (p.Arg563=) c.1659A= (p.Arg553=) c.1644A= (p.Arg548=) n.671A= | |
| 7 | g.17339514A>C | CA366894969 | AHR | c.1689A>C (p.Arg563Ser) c.1659A>C (p.Arg553Ser) c.1644A>C (p.Arg548Ser) n.671A>C | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.17339514A>G | CA454134122 | AHR | c.1689A>G (p.Arg563=) c.1659A>G (p.Arg553=) c.1644A>G (p.Arg548=) n.671A>G | |
| 7 | g.17339514A>T | CA366894970 | AHR | c.1689A>T (p.Arg563Ser) c.1659A>T (p.Arg553Ser) c.1644A>T (p.Arg548Ser) n.671A>T | |
| 7 | g.17339515A>C | CA366894972 | AHR | c.1690A>C (p.Asn564His) c.1660A>C (p.Asn554His) c.1645A>C (p.Asn549His) n.672A>C | |
| 7 | g.17339515A>G | CA366894973 | AHR | c.1690A>G (p.Asn564Asp) c.1660A>G (p.Asn554Asp) c.1645A>G (p.Asn549Asp) n.672A>G | |
| 7 | g.17339515A>T | CA366894974 | AHR | c.1690A>T (p.Asn564Tyr) c.1660A>T (p.Asn554Tyr) c.1645A>T (p.Asn549Tyr) n.672A>T | COSMIC |
| 7 | g.17339516A>C | CA366894975 | AHR | c.1691A>C (p.Asn564Thr) c.1661A>C (p.Asn554Thr) c.1646A>C (p.Asn549Thr) n.673A>C | |
| 7 | g.17339516A>G | CA366894976 | AHR | c.1691A>G (p.Asn564Ser) c.1661A>G (p.Asn554Ser) c.1646A>G (p.Asn549Ser) n.673A>G | |
| 7 | g.17339516A>T | CA366894977 | AHR | c.1691A>T (p.Asn564Ile) c.1661A>T (p.Asn554Ile) c.1646A>T (p.Asn549Ile) n.673A>T | |
| 7 | g.17339517T>A | CA366894978 | AHR | c.1692T>A (p.Asn564Lys) c.1662T>A (p.Asn554Lys) c.1647T>A (p.Asn549Lys) n.674T>A | |
| 7 | g.17339517T>C | CA454134123 | AHR | c.1692T>C (p.Asn564=) c.1662T>C (p.Asn554=) c.1647T>C (p.Asn549=) n.674T>C | gnomAD v4 |
| 7 | g.17339517T>G | CA366894979 | AHR | c.1692T>G (p.Asn564Lys) c.1662T>G (p.Asn554Lys) c.1647T>G (p.Asn549Lys) n.674T>G | |
| 7 | g.17339518G>A | CA366894980 | AHR | c.1693G>A (p.Asp565Asn) c.1663G>A (p.Asp555Asn) c.1648G>A (p.Asp550Asn) n.675G>A | |
| 7 | g.17339518G>C | CA366894981 | AHR | c.1693G>C (p.Asp565His) c.1663G>C (p.Asp555His) c.1648G>C (p.Asp550His) n.675G>C | |
| 7 | g.17339518G>T | CA366894982 | AHR | c.1693G>T (p.Asp565Tyr) c.1663G>T (p.Asp555Tyr) c.1648G>T (p.Asp550Tyr) n.675G>T | gnomAD v4 |
| 7 | g.17339519A= | CA1691323862 | AHR | c.1694A= (p.Asp565=) c.1664A= (p.Asp555=) c.1649A= (p.Asp550=) n.676A= | |
| 7 | g.17339519A>C | CA366894985 | AHR | c.1694A>C (p.Asp565Ala) c.1664A>C (p.Asp555Ala) c.1649A>C (p.Asp550Ala) n.676A>C | |
| 7 | g.17339519A>G | CA366894984 | AHR | c.1694A>G (p.Asp565Gly) c.1664A>G (p.Asp555Gly) c.1649A>G (p.Asp550Gly) n.676A>G | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.17339519A>T | CA366894983 | AHR | c.1694A>T (p.Asp565Val) c.1664A>T (p.Asp555Val) c.1649A>T (p.Asp550Val) n.676A>T | |
| 7 | g.17339520T>A | CA366894986 | AHR | c.1695T>A (p.Asp565Glu) c.1665T>A (p.Asp555Glu) c.1650T>A (p.Asp550Glu) n.677T>A | |
| 7 | g.17339520T>C | CA454134124 | AHR | c.1695T>C (p.Asp565=) c.1665T>C (p.Asp555=) c.1650T>C (p.Asp550=) n.677T>C | |
| 7 | g.17339520T>G | CA366894987 | AHR | c.1695T>G (p.Asp565Glu) c.1665T>G (p.Asp555Glu) c.1650T>G (p.Asp550Glu) n.677T>G | |
| 7 | g.17339521T>A | CA366894988 | AHR | c.1696T>A (p.Phe566Ile) c.1666T>A (p.Phe556Ile) c.1651T>A (p.Phe551Ile) n.678T>A | gnomAD v4 |
| 7 | g.17339521T>C | CA366894989 | AHR | c.1696T>C (p.Phe566Leu) c.1666T>C (p.Phe556Leu) c.1651T>C (p.Phe551Leu) n.678T>C | |
| 7 | g.17339521T>G | CA366894990 | AHR | c.1696T>G (p.Phe566Val) c.1666T>G (p.Phe556Val) c.1651T>G (p.Phe551Val) n.678T>G | |
| 7 | g.17339522T>A | CA366894991 | AHR | c.1697T>A (p.Phe566Tyr) c.1667T>A (p.Phe556Tyr) c.1652T>A (p.Phe551Tyr) n.679T>A | |
| 7 | g.17339522T>C | CA366894992 | AHR | c.1697T>C (p.Phe566Ser) c.1667T>C (p.Phe556Ser) c.1652T>C (p.Phe551Ser) n.679T>C | |
| 7 | g.17339522T>G | CA366894993 | AHR | c.1697T>G (p.Phe566Cys) c.1667T>G (p.Phe556Cys) c.1652T>G (p.Phe551Cys) n.679T>G | |
| 7 | g.17339523T>A | CA366894994 | AHR | c.1698T>A (p.Phe566Leu) c.1668T>A (p.Phe556Leu) c.1653T>A (p.Phe551Leu) n.680T>A | |
| 7 | g.17339523T>C | CA454134125 | AHR | c.1698T>C (p.Phe566=) c.1668T>C (p.Phe556=) c.1653T>C (p.Phe551=) n.680T>C | |
| 7 | g.17339523T>G | CA366894995 | AHR | c.1698T>G (p.Phe566Leu) c.1668T>G (p.Phe556Leu) c.1653T>G (p.Phe551Leu) n.680T>G | |
| 7 | g.17339524T>A | CA366894996 | AHR | c.1699T>A (p.Ser567Thr) c.1669T>A (p.Ser557Thr) c.1654T>A (p.Ser552Thr) n.681T>A | |
| 7 | g.17339524T>C | CA366894997 | AHR | c.1699T>C (p.Ser567Pro) c.1669T>C (p.Ser557Pro) c.1654T>C (p.Ser552Pro) n.681T>C | |
| 7 | g.17339524T>G | CA366894998 | AHR | c.1699T>G (p.Ser567Ala) c.1669T>G (p.Ser557Ala) c.1654T>G (p.Ser552Ala) n.681T>G | |
| 7 | g.17339525C>A | CA366895000 | AHR | c.1700C>A (p.Ser567Tyr) c.1670C>A (p.Ser557Tyr) c.1655C>A (p.Ser552Tyr) n.682C>A | |
| 7 | g.17339525C= | CA1691323863 | AHR | c.1700C= (p.Ser567=) c.1670C= (p.Ser557=) c.1655C= (p.Ser552=) n.682C= | |
| 7 | g.17339525C>G | CA4172167 | AHR | c.1700C>G (p.Ser567Cys) c.1670C>G (p.Ser557Cys) c.1655C>G (p.Ser552Cys) n.682C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.17339525C>T | CA366894999 | AHR | c.1700C>T (p.Ser567Phe) c.1670C>T (p.Ser557Phe) c.1655C>T (p.Ser552Phe) n.682C>T | |
| 7 | g.17339526T>A | CA454134126 | AHR | c.1701T>A (p.Ser567=) c.1671T>A (p.Ser557=) c.1656T>A (p.Ser552=) n.683T>A | |
| 7 | g.17339526T>C | CA454134128 | AHR | c.1701T>C (p.Ser567=) c.1671T>C (p.Ser557=) c.1656T>C (p.Ser552=) n.683T>C | |
| 7 | g.17339526T>G | CA454134127 | AHR | c.1701T>G (p.Ser567=) c.1671T>G (p.Ser557=) c.1656T>G (p.Ser552=) n.683T>G | |
| 7 | g.17339527G>A | CA366895003 | AHR | c.1702G>A (p.Gly568Ser) c.1672G>A (p.Gly558Ser) c.1657G>A (p.Gly553Ser) n.684G>A | COSMIC |
| 7 | g.17339527G>C | CA366895001 | AHR | c.1702G>C (p.Gly568Arg) c.1672G>C (p.Gly558Arg) c.1657G>C (p.Gly553Arg) n.684G>C | |
| 7 | g.17339527G>T | CA366895002 | AHR | c.1702G>T (p.Gly568Cys) c.1672G>T (p.Gly558Cys) c.1657G>T (p.Gly553Cys) n.684G>T | |
| 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 |