Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.28208069A>GCA15857491HERC2c.7070-1687T>C (p.=)
c.6956-1687T>C (p.=)
c.7055-1687T>C (p.=)
c.6812-1687T>C (p.=)
c.6587-1687T>C (p.=)
c.4586-1687T>C (p.=)
c.3815-1687T>C (p.=)
c.1187-1687T>C (p.=)
n.7199-1687T>C
c.236-1687T>C (p.=)
n.7200-1687T>C
dbSNP gnomAD
15g.28208072C>ACA968037923HERC2c.7070-1690G>T (p.=)
c.6956-1690G>T (p.=)
c.7055-1690G>T (p.=)
c.6812-1690G>T (p.=)
c.6587-1690G>T (p.=)
c.4586-1690G>T (p.=)
c.3815-1690G>T (p.=)
c.1187-1690G>T (p.=)
n.7199-1690G>T
c.236-1690G>T (p.=)
n.7200-1690G>T
15g.28208072C>TCA711740169HERC2c.7070-1690G>A (p.=)
c.6956-1690G>A (p.=)
c.7055-1690G>A (p.=)
c.6812-1690G>A (p.=)
c.6587-1690G>A (p.=)
c.4586-1690G>A (p.=)
c.3815-1690G>A (p.=)
c.1187-1690G>A (p.=)
n.7199-1690G>A
c.236-1690G>A (p.=)
n.7200-1690G>A
15g.28208072_28208073insGCA968037924HERC2c.7070-1691_7070-1690insC (p.=)
c.6956-1691_6956-1690insC (p.=)
c.7055-1691_7055-1690insC (p.=)
c.6812-1691_6812-1690insC (p.=)
c.6587-1691_6587-1690insC (p.=)
c.4586-1691_4586-1690insC (p.=)
c.3815-1691_3815-1690insC (p.=)
c.1187-1691_1187-1690insC (p.=)
n.7199-1691_7199-1690insC
c.236-1691_236-1690insC (p.=)
n.7200-1691_7200-1690insC
15g.28208081T>CCA267947563HERC2c.7070-1699A>G (p.=)
c.6956-1699A>G (p.=)
c.7055-1699A>G (p.=)
c.6812-1699A>G (p.=)
c.6587-1699A>G (p.=)
c.4586-1699A>G (p.=)
c.3815-1699A>G (p.=)
c.1187-1699A>G (p.=)
n.7199-1699A>G
c.236-1699A>G (p.=)
n.7200-1699A>G
dbSNP gnomAD
15g.28208084A>CCA616718312HERC2c.7070-1702T>G (p.=)
c.6956-1702T>G (p.=)
c.7055-1702T>G (p.=)
c.6812-1702T>G (p.=)
c.6587-1702T>G (p.=)
c.4586-1702T>G (p.=)
c.3815-1702T>G (p.=)
c.1187-1702T>G (p.=)
n.7199-1702T>G
c.236-1702T>G (p.=)
n.7200-1702T>G
gnomAD
15g.28208084A>GCA968037926HERC2c.7070-1702T>C (p.=)
c.6956-1702T>C (p.=)
c.7055-1702T>C (p.=)
c.6812-1702T>C (p.=)
c.6587-1702T>C (p.=)
c.4586-1702T>C (p.=)
c.3815-1702T>C (p.=)
c.1187-1702T>C (p.=)
n.7199-1702T>C
c.236-1702T>C (p.=)
n.7200-1702T>C
15g.28208086T>CCA711740178HERC2c.7070-1704A>G (p.=)
c.6956-1704A>G (p.=)
c.7055-1704A>G (p.=)
c.6812-1704A>G (p.=)
c.6587-1704A>G (p.=)
c.4586-1704A>G (p.=)
c.3815-1704A>G (p.=)
c.1187-1704A>G (p.=)
n.7199-1704A>G
c.236-1704A>G (p.=)
n.7200-1704A>G
15g.28208086T>GCA968037933HERC2c.7070-1704A>C (p.=)
c.6956-1704A>C (p.=)
c.7055-1704A>C (p.=)
c.6812-1704A>C (p.=)
c.6587-1704A>C (p.=)
c.4586-1704A>C (p.=)
c.3815-1704A>C (p.=)
c.1187-1704A>C (p.=)
n.7199-1704A>C
c.236-1704A>C (p.=)
n.7200-1704A>C
15g.28208087C>ACA968037936HERC2c.7070-1705G>T (p.=)
c.6956-1705G>T (p.=)
c.7055-1705G>T (p.=)
c.6812-1705G>T (p.=)
c.6587-1705G>T (p.=)
c.4586-1705G>T (p.=)
c.3815-1705G>T (p.=)
c.1187-1705G>T (p.=)
n.7199-1705G>T
c.236-1705G>T (p.=)
n.7200-1705G>T
15g.28208089C>TCA711740181HERC2c.7070-1707G>A (p.=)
c.6956-1707G>A (p.=)
c.7055-1707G>A (p.=)
c.6812-1707G>A (p.=)
c.6587-1707G>A (p.=)
c.4586-1707G>A (p.=)
c.3815-1707G>A (p.=)
c.1187-1707G>A (p.=)
n.7199-1707G>A
c.236-1707G>A (p.=)
n.7200-1707G>A
15g.28208091A>GCA267947565HERC2c.7070-1709T>C (p.=)
c.6956-1709T>C (p.=)
c.7055-1709T>C (p.=)
c.6812-1709T>C (p.=)
c.6587-1709T>C (p.=)
c.4586-1709T>C (p.=)
c.3815-1709T>C (p.=)
c.1187-1709T>C (p.=)
n.7199-1709T>C
c.236-1709T>C (p.=)
n.7200-1709T>C
dbSNP
15g.28208094A>CCA968037943HERC2c.7070-1712T>G (p.=)
c.6956-1712T>G (p.=)
c.7055-1712T>G (p.=)
c.6812-1712T>G (p.=)
c.6587-1712T>G (p.=)
c.4586-1712T>G (p.=)
c.3815-1712T>G (p.=)
c.1187-1712T>G (p.=)
n.7199-1712T>G
c.236-1712T>G (p.=)
n.7200-1712T>G
15g.28208098G>ACA267947579HERC2c.7070-1716C>T (p.=)
c.6956-1716C>T (p.=)
c.7055-1716C>T (p.=)
c.6812-1716C>T (p.=)
c.6587-1716C>T (p.=)
c.4586-1716C>T (p.=)
c.3815-1716C>T (p.=)
c.1187-1716C>T (p.=)
n.7199-1716C>T
c.236-1716C>T (p.=)
n.7200-1716C>T
dbSNP gnomAD
15g.28208101A>GCA711740185HERC2c.7070-1719T>C (p.=)
c.6956-1719T>C (p.=)
c.7055-1719T>C (p.=)
c.6812-1719T>C (p.=)
c.6587-1719T>C (p.=)
c.4586-1719T>C (p.=)
c.3815-1719T>C (p.=)
c.1187-1719T>C (p.=)
n.7199-1719T>C
c.236-1719T>C (p.=)
n.7200-1719T>C
15g.28208103T>CCA616718315HERC2c.7070-1721A>G (p.=)
c.6956-1721A>G (p.=)
c.7055-1721A>G (p.=)
c.6812-1721A>G (p.=)
c.6587-1721A>G (p.=)
c.4586-1721A>G (p.=)
c.3815-1721A>G (p.=)
c.1187-1721A>G (p.=)
n.7199-1721A>G
c.236-1721A>G (p.=)
n.7200-1721A>G
gnomAD
15g.28208106T>CCA711740188HERC2c.7070-1724A>G (p.=)
c.6956-1724A>G (p.=)
c.7055-1724A>G (p.=)
c.6812-1724A>G (p.=)
c.6587-1724A>G (p.=)
c.4586-1724A>G (p.=)
c.3815-1724A>G (p.=)
c.1187-1724A>G (p.=)
n.7199-1724A>G
c.236-1724A>G (p.=)
n.7200-1724A>G
15g.28208107C>TCA267947585HERC2c.7070-1725G>A (p.=)
c.6956-1725G>A (p.=)
c.7055-1725G>A (p.=)
c.6812-1725G>A (p.=)
c.6587-1725G>A (p.=)
c.4586-1725G>A (p.=)
c.3815-1725G>A (p.=)
c.1187-1725G>A (p.=)
n.7199-1725G>A
c.236-1725G>A (p.=)
n.7200-1725G>A
dbSNP
15g.28208112T>ACA616718316HERC2c.7070-1730A>T (p.=)
c.6956-1730A>T (p.=)
c.7055-1730A>T (p.=)
c.6812-1730A>T (p.=)
c.6587-1730A>T (p.=)
c.4586-1730A>T (p.=)
c.3815-1730A>T (p.=)
c.1187-1730A>T (p.=)
n.7199-1730A>T
c.236-1730A>T (p.=)
n.7200-1730A>T
gnomAD
15g.28208117A>CCA711740210HERC2c.7070-1735T>G (p.=)
c.6956-1735T>G (p.=)
c.7055-1735T>G (p.=)
c.6812-1735T>G (p.=)
c.6587-1735T>G (p.=)
c.4586-1735T>G (p.=)
c.3815-1735T>G (p.=)
c.1187-1735T>G (p.=)
n.7199-1735T>G
c.236-1735T>G (p.=)
n.7200-1735T>G
15g.28208118T>ACA711740216HERC2c.7070-1736A>T (p.=)
c.6956-1736A>T (p.=)
c.7055-1736A>T (p.=)
c.6812-1736A>T (p.=)
c.6587-1736A>T (p.=)
c.4586-1736A>T (p.=)
c.3815-1736A>T (p.=)
c.1187-1736A>T (p.=)
n.7199-1736A>T
c.236-1736A>T (p.=)
n.7200-1736A>T
15g.28208118T>CCA616718318HERC2c.7070-1736A>G (p.=)
c.6956-1736A>G (p.=)
c.7055-1736A>G (p.=)
c.6812-1736A>G (p.=)
c.6587-1736A>G (p.=)
c.4586-1736A>G (p.=)
c.3815-1736A>G (p.=)
c.1187-1736A>G (p.=)
n.7199-1736A>G
c.236-1736A>G (p.=)
n.7200-1736A>G
gnomAD
15g.28208119A>GCA616718320HERC2c.7070-1737T>C (p.=)
c.6956-1737T>C (p.=)
c.7055-1737T>C (p.=)
c.6812-1737T>C (p.=)
c.6587-1737T>C (p.=)
c.4586-1737T>C (p.=)
c.3815-1737T>C (p.=)
c.1187-1737T>C (p.=)
n.7199-1737T>C
c.236-1737T>C (p.=)
n.7200-1737T>C
gnomAD
15g.28208121C>ACA968037954HERC2c.7070-1739G>T (p.=)
c.6956-1739G>T (p.=)
c.7055-1739G>T (p.=)
c.6812-1739G>T (p.=)
c.6587-1739G>T (p.=)
c.4586-1739G>T (p.=)
c.3815-1739G>T (p.=)
c.1187-1739G>T (p.=)
n.7199-1739G>T
c.236-1739G>T (p.=)
n.7200-1739G>T
15g.28208122C>GCA267947590HERC2c.7070-1740G>C (p.=)
c.6956-1740G>C (p.=)
c.7055-1740G>C (p.=)
c.6812-1740G>C (p.=)
c.6587-1740G>C (p.=)
c.4586-1740G>C (p.=)
c.3815-1740G>C (p.=)
c.1187-1740G>C (p.=)
n.7199-1740G>C
c.236-1740G>C (p.=)
n.7200-1740G>C
dbSNP gnomAD
15g.28208128T>GCA711740227HERC2c.7070-1746A>C (p.=)
c.6956-1746A>C (p.=)
c.7055-1746A>C (p.=)
c.6812-1746A>C (p.=)
c.6587-1746A>C (p.=)
c.4586-1746A>C (p.=)
c.3815-1746A>C (p.=)
c.1187-1746A>C (p.=)
n.7199-1746A>C
c.236-1746A>C (p.=)
n.7200-1746A>C
15g.28208135T>GCA267947608HERC2c.7070-1753A>C (p.=)
c.6956-1753A>C (p.=)
c.7055-1753A>C (p.=)
c.6812-1753A>C (p.=)
c.6587-1753A>C (p.=)
c.4586-1753A>C (p.=)
c.3815-1753A>C (p.=)
c.1187-1753A>C (p.=)
n.7199-1753A>C
c.236-1753A>C (p.=)
n.7200-1753A>C
dbSNP
15g.28208144A>GCA656064958HERC2c.7070-1762T>C (p.=)
c.6956-1762T>C (p.=)
c.7055-1762T>C (p.=)
c.6812-1762T>C (p.=)
c.6587-1762T>C (p.=)
c.4586-1762T>C (p.=)
c.3815-1762T>C (p.=)
c.1187-1762T>C (p.=)
n.7199-1762T>C
c.236-1762T>C (p.=)
n.7200-1762T>C
COSMIC
15g.28208145C>GCA267947617HERC2c.7070-1763G>C (p.=)
c.6956-1763G>C (p.=)
c.7055-1763G>C (p.=)
c.6812-1763G>C (p.=)
c.6587-1763G>C (p.=)
c.4586-1763G>C (p.=)
c.3815-1763G>C (p.=)
c.1187-1763G>C (p.=)
n.7199-1763G>C
c.236-1763G>C (p.=)
n.7200-1763G>C
dbSNP
15g.28208152T>CCA968037958HERC2c.7070-1770A>G (p.=)
c.6956-1770A>G (p.=)
c.7055-1770A>G (p.=)
c.6812-1770A>G (p.=)
c.6587-1770A>G (p.=)
c.4586-1770A>G (p.=)
c.3815-1770A>G (p.=)
c.1187-1770A>G (p.=)
n.7199-1770A>G
c.236-1770A>G (p.=)
n.7200-1770A>G
15g.28208154G>ACA711740230HERC2c.7070-1772C>T (p.=)
c.6956-1772C>T (p.=)
c.7055-1772C>T (p.=)
c.6812-1772C>T (p.=)
c.6587-1772C>T (p.=)
c.4586-1772C>T (p.=)
c.3815-1772C>T (p.=)
c.1187-1772C>T (p.=)
n.7199-1772C>T
c.236-1772C>T (p.=)
n.7200-1772C>T
15g.28208159C>ACA267947620HERC2c.7070-1777G>T (p.=)
c.6956-1777G>T (p.=)
c.7055-1777G>T (p.=)
c.6812-1777G>T (p.=)
c.6587-1777G>T (p.=)
c.4586-1777G>T (p.=)
c.3815-1777G>T (p.=)
c.1187-1777G>T (p.=)
n.7199-1777G>T
c.236-1777G>T (p.=)
n.7200-1777G>T
dbSNP gnomAD
15g.28208162T>CCA656064959HERC2c.7070-1780A>G (p.=)
c.6956-1780A>G (p.=)
c.7055-1780A>G (p.=)
c.6812-1780A>G (p.=)
c.6587-1780A>G (p.=)
c.4586-1780A>G (p.=)
c.3815-1780A>G (p.=)
c.1187-1780A>G (p.=)
n.7199-1780A>G
c.236-1780A>G (p.=)
n.7200-1780A>G
COSMIC
15g.28208164A>TCA968037962HERC2c.7070-1782T>A (p.=)
c.6956-1782T>A (p.=)
c.7055-1782T>A (p.=)
c.6812-1782T>A (p.=)
c.6587-1782T>A (p.=)
c.4586-1782T>A (p.=)
c.3815-1782T>A (p.=)
c.1187-1782T>A (p.=)
n.7199-1782T>A
c.236-1782T>A (p.=)
n.7200-1782T>A

Number of alleles fetched