Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.28208069A>G | CA15857491 | HERC2 | c.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 |
15 | g.28208072C>A | CA968037923 | HERC2 | c.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 | |
15 | g.28208072C>T | CA711740169 | HERC2 | c.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 | |
15 | g.28208072_28208073insG | CA968037924 | HERC2 | c.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 | |
15 | g.28208081T>C | CA267947563 | HERC2 | c.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 |
15 | g.28208084A>C | CA616718312 | HERC2 | c.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 |
15 | g.28208084A>G | CA968037926 | HERC2 | c.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 | |
15 | g.28208086T>C | CA711740178 | HERC2 | c.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 | |
15 | g.28208086T>G | CA968037933 | HERC2 | c.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 | |
15 | g.28208087C>A | CA968037936 | HERC2 | c.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 | |
15 | g.28208089C>T | CA711740181 | HERC2 | c.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 | |
15 | g.28208091A>G | CA267947565 | HERC2 | c.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 |
15 | g.28208094A>C | CA968037943 | HERC2 | c.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 | |
15 | g.28208098G>A | CA267947579 | HERC2 | c.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 |
15 | g.28208101A>G | CA711740185 | HERC2 | c.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 | |
15 | g.28208103T>C | CA616718315 | HERC2 | c.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 |
15 | g.28208106T>C | CA711740188 | HERC2 | c.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 | |
15 | g.28208107C>T | CA267947585 | HERC2 | c.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 |
15 | g.28208112T>A | CA616718316 | HERC2 | c.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 |
15 | g.28208117A>C | CA711740210 | HERC2 | c.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 | |
15 | g.28208118T>A | CA711740216 | HERC2 | c.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 | |
15 | g.28208118T>C | CA616718318 | HERC2 | c.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 |
15 | g.28208119A>G | CA616718320 | HERC2 | c.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 |
15 | g.28208121C>A | CA968037954 | HERC2 | c.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 | |
15 | g.28208122C>G | CA267947590 | HERC2 | c.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 |
15 | g.28208128T>G | CA711740227 | HERC2 | c.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 | |
15 | g.28208135T>G | CA267947608 | HERC2 | c.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 |
15 | g.28208144A>G | CA656064958 | HERC2 | c.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 |
15 | g.28208145C>G | CA267947617 | HERC2 | c.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 |
15 | g.28208152T>C | CA968037958 | HERC2 | c.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 | |
15 | g.28208154G>A | CA711740230 | HERC2 | c.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 | |
15 | g.28208159C>A | CA267947620 | HERC2 | c.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 |
15 | g.28208162T>C | CA656064959 | HERC2 | c.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 |
15 | g.28208164A>T | CA968037962 | HERC2 | c.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 |