| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.17339486G>A | CA4172163 | AHR | c.1661G>A (p.Arg554Lys) c.1631G>A (p.Arg544Lys) c.1616G>A (p.Arg539Lys) n.643G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.17339486G>C | CA366894884 | AHR | c.1661G>C (p.Arg554Thr) c.1631G>C (p.Arg544Thr) c.1616G>C (p.Arg539Thr) n.643G>C | |
| 7 | g.17339486G= | CA1691323850 | AHR | c.1661G= (p.Arg554=) c.1631G= (p.Arg544=) c.1616G= (p.Arg539=) n.643G= | |
| 7 | g.17339486G>T | CA366894885 | AHR | c.1661G>T (p.Arg554Ile) c.1631G>T (p.Arg544Ile) c.1616G>T (p.Arg539Ile) n.643G>T | gnomAD v4 |
| 7 | g.17339487A= | CA1691323851 | AHR | c.1662A= (p.Arg554=) c.1632A= (p.Arg544=) c.1617A= (p.Arg539=) n.644A= | |
| 7 | g.17339487A>C | CA4172164 | AHR | c.1662A>C (p.Arg554Ser) c.1632A>C (p.Arg544Ser) c.1617A>C (p.Arg539Ser) n.644A>C | dbSNP ExAC gnomAD v2 |
| 7 | g.17339487A>G | CA4172165 | AHR | c.1662A>G (p.Arg554=) c.1632A>G (p.Arg544=) c.1617A>G (p.Arg539=) n.644A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.17339487A>T | CA366894889 | AHR | c.1662A>T (p.Arg554Ser) c.1632A>T (p.Arg544Ser) c.1617A>T (p.Arg539Ser) n.644A>T | dbSNP |
| 7 | g.17339488C>A | CA366894891 | AHR | c.1663C>A (p.His555Asn) c.1633C>A (p.His545Asn) c.1618C>A (p.His540Asn) n.645C>A | |
| 7 | g.17339488C= | CA1691323852 | AHR | c.1663C= (p.His555=) c.1633C= (p.His545=) c.1618C= (p.His540=) n.645C= | |
| 7 | g.17339488C>G | CA366894893 | AHR | c.1663C>G (p.His555Asp) c.1633C>G (p.His545Asp) c.1618C>G (p.His540Asp) n.645C>G | |
| 7 | g.17339488C>T | CA4172166 | AHR | c.1663C>T (p.His555Tyr) c.1633C>T (p.His545Tyr) c.1618C>T (p.His540Tyr) n.645C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.17339489A>C | CA366894896 | AHR | c.1664A>C (p.His555Pro) c.1634A>C (p.His545Pro) c.1619A>C (p.His540Pro) n.646A>C | gnomAD v4 |
| 7 | g.17339489A>G | CA366894898 | AHR | c.1664A>G (p.His555Arg) c.1634A>G (p.His545Arg) c.1619A>G (p.His540Arg) n.646A>G | gnomAD v4 |
| 7 | g.17339489A>T | CA366894900 | AHR | c.1664A>T (p.His555Leu) c.1634A>T (p.His545Leu) c.1619A>T (p.His540Leu) n.646A>T | |
| 7 | g.17339490C>A | CA366894901 | AHR | c.1665C>A (p.His555Gln) c.1635C>A (p.His545Gln) c.1620C>A (p.His540Gln) n.647C>A | |
| 7 | g.17339490C= | CA1691323853 | AHR | c.1665C= (p.His555=) c.1635C= (p.His545=) c.1620C= (p.His540=) n.647C= | |
| 7 | g.17339490C>G | CA366894903 | AHR | c.1665C>G (p.His555Gln) c.1635C>G (p.His545Gln) c.1620C>G (p.His540Gln) n.647C>G | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.17339490C>T | CA454134114 | AHR | c.1665C>T (p.His555=) c.1635C>T (p.His545=) c.1620C>T (p.His540=) n.647C>T | gnomAD v4 |
| 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 |