Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.28207974G>ACA968037850HERC2c.7070-1592C>T (p.=)
c.6956-1592C>T (p.=)
c.7055-1592C>T (p.=)
c.6812-1592C>T (p.=)
c.6587-1592C>T (p.=)
c.4586-1592C>T (p.=)
c.3815-1592C>T (p.=)
c.1187-1592C>T (p.=)
n.7199-1592C>T
c.236-1592C>T (p.=)
n.7200-1592C>T
15g.28207977C>GCA267947470HERC2c.7070-1595G>C (p.=)
c.6956-1595G>C (p.=)
c.7055-1595G>C (p.=)
c.6812-1595G>C (p.=)
c.6587-1595G>C (p.=)
c.4586-1595G>C (p.=)
c.3815-1595G>C (p.=)
c.1187-1595G>C (p.=)
n.7199-1595G>C
c.236-1595G>C (p.=)
n.7200-1595G>C
dbSNP
15g.28207977C>TCA711740110HERC2c.7070-1595G>A (p.=)
c.6956-1595G>A (p.=)
c.7055-1595G>A (p.=)
c.6812-1595G>A (p.=)
c.6587-1595G>A (p.=)
c.4586-1595G>A (p.=)
c.3815-1595G>A (p.=)
c.1187-1595G>A (p.=)
n.7199-1595G>A
c.236-1595G>A (p.=)
n.7200-1595G>A
15g.28207978G>ACA488971605HERC2c.7070-1596C>T (p.=)
c.6956-1596C>T (p.=)
c.7055-1596C>T (p.=)
c.6812-1596C>T (p.=)
c.6587-1596C>T (p.=)
c.4586-1596C>T (p.=)
c.3815-1596C>T (p.=)
c.1187-1596C>T (p.=)
n.7199-1596C>T
c.236-1596C>T (p.=)
n.7200-1596C>T
gnomAD
15g.28207978G>CCA616718298HERC2c.7070-1596C>G (p.=)
c.6956-1596C>G (p.=)
c.7055-1596C>G (p.=)
c.6812-1596C>G (p.=)
c.6587-1596C>G (p.=)
c.4586-1596C>G (p.=)
c.3815-1596C>G (p.=)
c.1187-1596C>G (p.=)
n.7199-1596C>G
c.236-1596C>G (p.=)
n.7200-1596C>G
gnomAD
15g.28207978G>TCA656064954HERC2c.7070-1596C>A (p.=)
c.6956-1596C>A (p.=)
c.7055-1596C>A (p.=)
c.6812-1596C>A (p.=)
c.6587-1596C>A (p.=)
c.4586-1596C>A (p.=)
c.3815-1596C>A (p.=)
c.1187-1596C>A (p.=)
n.7199-1596C>A
c.236-1596C>A (p.=)
n.7200-1596C>A
COSMIC
15g.28207986G>CCA711740115HERC2c.7070-1604C>G (p.=)
c.6956-1604C>G (p.=)
c.7055-1604C>G (p.=)
c.6812-1604C>G (p.=)
c.6587-1604C>G (p.=)
c.4586-1604C>G (p.=)
c.3815-1604C>G (p.=)
c.1187-1604C>G (p.=)
n.7199-1604C>G
c.236-1604C>G (p.=)
n.7200-1604C>G
15g.28207991G>TCA711740118HERC2c.7070-1609C>A (p.=)
c.6956-1609C>A (p.=)
c.7055-1609C>A (p.=)
c.6812-1609C>A (p.=)
c.6587-1609C>A (p.=)
c.4586-1609C>A (p.=)
c.3815-1609C>A (p.=)
c.1187-1609C>A (p.=)
n.7199-1609C>A
c.236-1609C>A (p.=)
n.7200-1609C>A
15g.28207993C>TCA968037855HERC2c.7070-1611G>A (p.=)
c.6956-1611G>A (p.=)
c.7055-1611G>A (p.=)
c.6812-1611G>A (p.=)
c.6587-1611G>A (p.=)
c.4586-1611G>A (p.=)
c.3815-1611G>A (p.=)
c.1187-1611G>A (p.=)
n.7199-1611G>A
c.236-1611G>A (p.=)
n.7200-1611G>A
15g.28207996G>CCA968037856HERC2c.7070-1614C>G (p.=)
c.6956-1614C>G (p.=)
c.7055-1614C>G (p.=)
c.6812-1614C>G (p.=)
c.6587-1614C>G (p.=)
c.4586-1614C>G (p.=)
c.3815-1614C>G (p.=)
c.1187-1614C>G (p.=)
n.7199-1614C>G
c.236-1614C>G (p.=)
n.7200-1614C>G
15g.28207998T>GCA267947471HERC2c.7070-1616A>C (p.=)
c.6956-1616A>C (p.=)
c.7055-1616A>C (p.=)
c.6812-1616A>C (p.=)
c.6587-1616A>C (p.=)
c.4586-1616A>C (p.=)
c.3815-1616A>C (p.=)
c.1187-1616A>C (p.=)
n.7199-1616A>C
c.236-1616A>C (p.=)
n.7200-1616A>C
dbSNP gnomAD
15g.28208002C>ACA711740120HERC2c.7070-1620G>T (p.=)
c.6956-1620G>T (p.=)
c.7055-1620G>T (p.=)
c.6812-1620G>T (p.=)
c.6587-1620G>T (p.=)
c.4586-1620G>T (p.=)
c.3815-1620G>T (p.=)
c.1187-1620G>T (p.=)
n.7199-1620G>T
c.236-1620G>T (p.=)
n.7200-1620G>T
15g.28208002C>TCA711740122HERC2c.7070-1620G>A (p.=)
c.6956-1620G>A (p.=)
c.7055-1620G>A (p.=)
c.6812-1620G>A (p.=)
c.6587-1620G>A (p.=)
c.4586-1620G>A (p.=)
c.3815-1620G>A (p.=)
c.1187-1620G>A (p.=)
n.7199-1620G>A
c.236-1620G>A (p.=)
n.7200-1620G>A
15g.28208004T>ACA267947473HERC2c.7070-1622A>T (p.=)
c.6956-1622A>T (p.=)
c.7055-1622A>T (p.=)
c.6812-1622A>T (p.=)
c.6587-1622A>T (p.=)
c.4586-1622A>T (p.=)
c.3815-1622A>T (p.=)
c.1187-1622A>T (p.=)
n.7199-1622A>T
c.236-1622A>T (p.=)
n.7200-1622A>T
dbSNP
15g.28208004T>CCA616718299HERC2c.7070-1622A>G (p.=)
c.6956-1622A>G (p.=)
c.7055-1622A>G (p.=)
c.6812-1622A>G (p.=)
c.6587-1622A>G (p.=)
c.4586-1622A>G (p.=)
c.3815-1622A>G (p.=)
c.1187-1622A>G (p.=)
n.7199-1622A>G
c.236-1622A>G (p.=)
n.7200-1622A>G
gnomAD
15g.28208012G>ACA267947475HERC2c.7070-1630C>T (p.=)
c.6956-1630C>T (p.=)
c.7055-1630C>T (p.=)
c.6812-1630C>T (p.=)
c.6587-1630C>T (p.=)
c.4586-1630C>T (p.=)
c.3815-1630C>T (p.=)
c.1187-1630C>T (p.=)
n.7199-1630C>T
c.236-1630C>T (p.=)
n.7200-1630C>T
dbSNP
15g.28208013T>CCA711740125HERC2c.7070-1631A>G (p.=)
c.6956-1631A>G (p.=)
c.7055-1631A>G (p.=)
c.6812-1631A>G (p.=)
c.6587-1631A>G (p.=)
c.4586-1631A>G (p.=)
c.3815-1631A>G (p.=)
c.1187-1631A>G (p.=)
n.7199-1631A>G
c.236-1631A>G (p.=)
n.7200-1631A>G
15g.28208019G>ACA711740128HERC2c.7070-1637C>T (p.=)
c.6956-1637C>T (p.=)
c.7055-1637C>T (p.=)
c.6812-1637C>T (p.=)
c.6587-1637C>T (p.=)
c.4586-1637C>T (p.=)
c.3815-1637C>T (p.=)
c.1187-1637C>T (p.=)
n.7199-1637C>T
c.236-1637C>T (p.=)
n.7200-1637C>T
15g.28208021C>ACA711740134HERC2c.7070-1639G>T (p.=)
c.6956-1639G>T (p.=)
c.7055-1639G>T (p.=)
c.6812-1639G>T (p.=)
c.6587-1639G>T (p.=)
c.4586-1639G>T (p.=)
c.3815-1639G>T (p.=)
c.1187-1639G>T (p.=)
n.7199-1639G>T
c.236-1639G>T (p.=)
n.7200-1639G>T
15g.28208023C>TCA711740138HERC2c.7070-1641G>A (p.=)
c.6956-1641G>A (p.=)
c.7055-1641G>A (p.=)
c.6812-1641G>A (p.=)
c.6587-1641G>A (p.=)
c.4586-1641G>A (p.=)
c.3815-1641G>A (p.=)
c.1187-1641G>A (p.=)
n.7199-1641G>A
c.236-1641G>A (p.=)
n.7200-1641G>A
15g.28208025G>CCA711740144HERC2c.7070-1643C>G (p.=)
c.6956-1643C>G (p.=)
c.7055-1643C>G (p.=)
c.6812-1643C>G (p.=)
c.6587-1643C>G (p.=)
c.4586-1643C>G (p.=)
c.3815-1643C>G (p.=)
c.1187-1643C>G (p.=)
n.7199-1643C>G
c.236-1643C>G (p.=)
n.7200-1643C>G
15g.28208026C>GCA711740147HERC2c.7070-1644G>C (p.=)
c.6956-1644G>C (p.=)
c.7055-1644G>C (p.=)
c.6812-1644G>C (p.=)
c.6587-1644G>C (p.=)
c.4586-1644G>C (p.=)
c.3815-1644G>C (p.=)
c.1187-1644G>C (p.=)
n.7199-1644G>C
c.236-1644G>C (p.=)
n.7200-1644G>C
15g.28208026C>TCA267947480HERC2c.7070-1644G>A (p.=)
c.6956-1644G>A (p.=)
c.7055-1644G>A (p.=)
c.6812-1644G>A (p.=)
c.6587-1644G>A (p.=)
c.4586-1644G>A (p.=)
c.3815-1644G>A (p.=)
c.1187-1644G>A (p.=)
n.7199-1644G>A
c.236-1644G>A (p.=)
n.7200-1644G>A
dbSNP
15g.28208031T>ACA267947484HERC2c.7070-1649A>T (p.=)
c.6956-1649A>T (p.=)
c.7055-1649A>T (p.=)
c.6812-1649A>T (p.=)
c.6587-1649A>T (p.=)
c.4586-1649A>T (p.=)
c.3815-1649A>T (p.=)
c.1187-1649A>T (p.=)
n.7199-1649A>T
c.236-1649A>T (p.=)
n.7200-1649A>T
dbSNP gnomAD
15g.28208031T>CCA711740150HERC2c.7070-1649A>G (p.=)
c.6956-1649A>G (p.=)
c.7055-1649A>G (p.=)
c.6812-1649A>G (p.=)
c.6587-1649A>G (p.=)
c.4586-1649A>G (p.=)
c.3815-1649A>G (p.=)
c.1187-1649A>G (p.=)
n.7199-1649A>G
c.236-1649A>G (p.=)
n.7200-1649A>G
15g.28208031T>GCA267947485HERC2c.7070-1649A>C (p.=)
c.6956-1649A>C (p.=)
c.7055-1649A>C (p.=)
c.6812-1649A>C (p.=)
c.6587-1649A>C (p.=)
c.4586-1649A>C (p.=)
c.3815-1649A>C (p.=)
c.1187-1649A>C (p.=)
n.7199-1649A>C
c.236-1649A>C (p.=)
n.7200-1649A>C
dbSNP gnomAD
15g.28208033G>ACA711740153HERC2c.7070-1651C>T (p.=)
c.6956-1651C>T (p.=)
c.7055-1651C>T (p.=)
c.6812-1651C>T (p.=)
c.6587-1651C>T (p.=)
c.4586-1651C>T (p.=)
c.3815-1651C>T (p.=)
c.1187-1651C>T (p.=)
n.7199-1651C>T
c.236-1651C>T (p.=)
n.7200-1651C>T
15g.28208033G>CCA616718304HERC2c.7070-1651C>G (p.=)
c.6956-1651C>G (p.=)
c.7055-1651C>G (p.=)
c.6812-1651C>G (p.=)
c.6587-1651C>G (p.=)
c.4586-1651C>G (p.=)
c.3815-1651C>G (p.=)
c.1187-1651C>G (p.=)
n.7199-1651C>G
c.236-1651C>G (p.=)
n.7200-1651C>G
gnomAD
15g.28208039G>ACA968037875HERC2c.7070-1657C>T (p.=)
c.6956-1657C>T (p.=)
c.7055-1657C>T (p.=)
c.6812-1657C>T (p.=)
c.6587-1657C>T (p.=)
c.4586-1657C>T (p.=)
c.3815-1657C>T (p.=)
c.1187-1657C>T (p.=)
n.7199-1657C>T
c.236-1657C>T (p.=)
n.7200-1657C>T
15g.28208041G>ACA968037877HERC2c.7070-1659C>T (p.=)
c.6956-1659C>T (p.=)
c.7055-1659C>T (p.=)
c.6812-1659C>T (p.=)
c.6587-1659C>T (p.=)
c.4586-1659C>T (p.=)
c.3815-1659C>T (p.=)
c.1187-1659C>T (p.=)
n.7199-1659C>T
c.236-1659C>T (p.=)
n.7200-1659C>T
15g.28208042C>ACA968037878HERC2c.7070-1660G>T (p.=)
c.6956-1660G>T (p.=)
c.7055-1660G>T (p.=)
c.6812-1660G>T (p.=)
c.6587-1660G>T (p.=)
c.4586-1660G>T (p.=)
c.3815-1660G>T (p.=)
c.1187-1660G>T (p.=)
n.7199-1660G>T
c.236-1660G>T (p.=)
n.7200-1660G>T
15g.28208044G>ACA267947527HERC2c.7070-1662C>T (p.=)
c.6956-1662C>T (p.=)
c.7055-1662C>T (p.=)
c.6812-1662C>T (p.=)
c.6587-1662C>T (p.=)
c.4586-1662C>T (p.=)
c.3815-1662C>T (p.=)
c.1187-1662C>T (p.=)
n.7199-1662C>T
c.236-1662C>T (p.=)
n.7200-1662C>T
dbSNP
15g.28208044G>TCA656064956HERC2c.7070-1662C>A (p.=)
c.6956-1662C>A (p.=)
c.7055-1662C>A (p.=)
c.6812-1662C>A (p.=)
c.6587-1662C>A (p.=)
c.4586-1662C>A (p.=)
c.3815-1662C>A (p.=)
c.1187-1662C>A (p.=)
n.7199-1662C>A
c.236-1662C>A (p.=)
n.7200-1662C>A
COSMIC
15g.28208049G>ACA968037883HERC2c.7070-1667C>T (p.=)
c.6956-1667C>T (p.=)
c.7055-1667C>T (p.=)
c.6812-1667C>T (p.=)
c.6587-1667C>T (p.=)
c.4586-1667C>T (p.=)
c.3815-1667C>T (p.=)
c.1187-1667C>T (p.=)
n.7199-1667C>T
c.236-1667C>T (p.=)
n.7200-1667C>T
15g.28208051A>CCA616718306HERC2c.7070-1669T>G (p.=)
c.6956-1669T>G (p.=)
c.7055-1669T>G (p.=)
c.6812-1669T>G (p.=)
c.6587-1669T>G (p.=)
c.4586-1669T>G (p.=)
c.3815-1669T>G (p.=)
c.1187-1669T>G (p.=)
n.7199-1669T>G
c.236-1669T>G (p.=)
n.7200-1669T>G
gnomAD
15g.28208054G>ACA711740160HERC2c.7070-1672C>T (p.=)
c.6956-1672C>T (p.=)
c.7055-1672C>T (p.=)
c.6812-1672C>T (p.=)
c.6587-1672C>T (p.=)
c.4586-1672C>T (p.=)
c.3815-1672C>T (p.=)
c.1187-1672C>T (p.=)
n.7199-1672C>T
c.236-1672C>T (p.=)
n.7200-1672C>T
15g.28208058A>GCA267947536HERC2c.7070-1676T>C (p.=)
c.6956-1676T>C (p.=)
c.7055-1676T>C (p.=)
c.6812-1676T>C (p.=)
c.6587-1676T>C (p.=)
c.4586-1676T>C (p.=)
c.3815-1676T>C (p.=)
c.1187-1676T>C (p.=)
n.7199-1676T>C
c.236-1676T>C (p.=)
n.7200-1676T>C
dbSNP gnomAD
15g.28208059T>ACA267947546HERC2c.7070-1677A>T (p.=)
c.6956-1677A>T (p.=)
c.7055-1677A>T (p.=)
c.6812-1677A>T (p.=)
c.6587-1677A>T (p.=)
c.4586-1677A>T (p.=)
c.3815-1677A>T (p.=)
c.1187-1677A>T (p.=)
n.7199-1677A>T
c.236-1677A>T (p.=)
n.7200-1677A>T
dbSNP
15g.28208060_28208061delCA968037906HERC2c.7070-1679_7070-1678del (p.=)
c.6956-1679_6956-1678del (p.=)
c.7055-1679_7055-1678del (p.=)
c.6812-1679_6812-1678del (p.=)
c.6587-1679_6587-1678del (p.=)
c.4586-1679_4586-1678del (p.=)
c.3815-1679_3815-1678del (p.=)
c.1187-1679_1187-1678del (p.=)
n.7199-1679_7199-1678del
c.236-1679_236-1678del (p.=)
n.7200-1679_7200-1678del
15g.28208061_28208062insTTTTTTCA968037909HERC2c.7070-1680_7070-1679insAAAAAA (p.=)
c.6956-1680_6956-1679insAAAAAA (p.=)
c.7055-1680_7055-1679insAAAAAA (p.=)
c.6812-1680_6812-1679insAAAAAA (p.=)
c.6587-1680_6587-1679insAAAAAA (p.=)
c.4586-1680_4586-1679insAAAAAA (p.=)
c.3815-1680_3815-1679insAAAAAA (p.=)
c.1187-1680_1187-1679insAAAAAA (p.=)
n.7199-1680_7199-1679insAAAAAA
c.236-1680_236-1679insAAAAAA (p.=)
n.7200-1680_7200-1679insAAAAAA
15g.28208064_28208065insGACA968037912HERC2c.7070-1683_7070-1682insTC (p.=)
c.6956-1683_6956-1682insTC (p.=)
c.7055-1683_7055-1682insTC (p.=)
c.6812-1683_6812-1682insTC (p.=)
c.6587-1683_6587-1682insTC (p.=)
c.4586-1683_4586-1682insTC (p.=)
c.3815-1683_3815-1682insTC (p.=)
c.1187-1683_1187-1682insTC (p.=)
n.7199-1683_7199-1682insTC
c.236-1683_236-1682insTC (p.=)
n.7200-1683_7200-1682insTC
15g.28208065T>CCA267947552HERC2c.7070-1683A>G (p.=)
c.6956-1683A>G (p.=)
c.7055-1683A>G (p.=)
c.6812-1683A>G (p.=)
c.6587-1683A>G (p.=)
c.4586-1683A>G (p.=)
c.3815-1683A>G (p.=)
c.1187-1683A>G (p.=)
n.7199-1683A>G
c.236-1683A>G (p.=)
n.7200-1683A>G
dbSNP gnomAD
15g.28208066C>ACA968037916HERC2c.7070-1684G>T (p.=)
c.6956-1684G>T (p.=)
c.7055-1684G>T (p.=)
c.6812-1684G>T (p.=)
c.6587-1684G>T (p.=)
c.4586-1684G>T (p.=)
c.3815-1684G>T (p.=)
c.1187-1684G>T (p.=)
n.7199-1684G>T
c.236-1684G>T (p.=)
n.7200-1684G>T
15g.28208068C>TCA616718309HERC2c.7070-1686G>A (p.=)
c.6956-1686G>A (p.=)
c.7055-1686G>A (p.=)
c.6812-1686G>A (p.=)
c.6587-1686G>A (p.=)
c.4586-1686G>A (p.=)
c.3815-1686G>A (p.=)
c.1187-1686G>A (p.=)
n.7199-1686G>A
c.236-1686G>A (p.=)
n.7200-1686G>A
gnomAD
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

Number of alleles fetched