Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38551486C>ACA352143027SCN5Ac.4883G>T (p.Arg1628Leu)
c.4886G>T (p.Arg1629Leu)
c.4832G>T (p.Arg1611Leu)
c.4724G>T (p.Arg1575Leu)
c.4787G>T (p.Arg1596Leu)
c.4757G>T (p.Arg1586Leu)
c.4829G>T (p.Arg1610Leu)
3g.38551486C=CA1358558196SCN5Ac.4883G= (p.Arg1628=)
c.4886G= (p.Arg1629=)
c.4832G= (p.Arg1611=)
c.4724G= (p.Arg1575=)
c.4787G= (p.Arg1596=)
c.4757G= (p.Arg1586=)
c.4829G= (p.Arg1610=)
3g.38551486C>GCA352143028SCN5Ac.4883G>C (p.Arg1628Pro)
c.4886G>C (p.Arg1629Pro)
c.4832G>C (p.Arg1611Pro)
c.4724G>C (p.Arg1575Pro)
c.4787G>C (p.Arg1596Pro)
c.4757G>C (p.Arg1586Pro)
c.4829G>C (p.Arg1610Pro)
3g.38551486C>TCA018714SCN5Ac.4883G>A (p.Arg1628Gln)
c.4886G>A (p.Arg1629Gln)
c.4832G>A (p.Arg1611Gln)
c.4724G>A (p.Arg1575Gln)
c.4787G>A (p.Arg1596Gln)
c.4757G>A (p.Arg1586Gln)
c.4829G>A (p.Arg1610Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38551487G>ACA063905SCN5Ac.4882C>T (p.Arg1628Ter)
c.4885C>T (p.Arg1629Ter)
c.4831C>T (p.Arg1611Ter)
c.4723C>T (p.Arg1575Ter)
c.4786C>T (p.Arg1596Ter)
c.4756C>T (p.Arg1586Ter)
c.4828C>T (p.Arg1610Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38551487G>CCA018709SCN5Ac.4882C>G (p.Arg1628Gly)
c.4885C>G (p.Arg1629Gly)
c.4831C>G (p.Arg1611Gly)
c.4723C>G (p.Arg1575Gly)
c.4786C>G (p.Arg1596Gly)
c.4756C>G (p.Arg1586Gly)
c.4828C>G (p.Arg1610Gly)
ClinVar dbSNP
3g.38551487G=CA1358558200SCN5Ac.4882C= (p.Arg1628=)
c.4885C= (p.Arg1629=)
c.4831C= (p.Arg1611=)
c.4723C= (p.Arg1575=)
c.4786C= (p.Arg1596=)
c.4756C= (p.Arg1586=)
c.4828C= (p.Arg1610=)
3g.38551487G>TCA433134278SCN5Ac.4882C>A (p.Arg1628=)
c.4885C>A (p.Arg1629=)
c.4831C>A (p.Arg1611=)
c.4723C>A (p.Arg1575=)
c.4786C>A (p.Arg1596=)
c.4756C>A (p.Arg1586=)
c.4828C>A (p.Arg1610=)
3g.38551488G>ACA433134280SCN5Ac.4881C>T (p.Ala1627=)
c.4884C>T (p.Ala1628=)
c.4830C>T (p.Ala1610=)
c.4722C>T (p.Ala1574=)
c.4785C>T (p.Ala1595=)
c.4755C>T (p.Ala1585=)
c.4827C>T (p.Ala1609=)
dbSNP gnomAD v2 gnomAD v4
3g.38551488G>CCA433134281SCN5Ac.4881C>G (p.Ala1627=)
c.4884C>G (p.Ala1628=)
c.4830C>G (p.Ala1610=)
c.4722C>G (p.Ala1574=)
c.4785C>G (p.Ala1595=)
c.4755C>G (p.Ala1585=)
c.4827C>G (p.Ala1609=)
3g.38551488G=CA1358558207SCN5Ac.4881C= (p.Ala1627=)
c.4884C= (p.Ala1628=)
c.4830C= (p.Ala1610=)
c.4722C= (p.Ala1574=)
c.4785C= (p.Ala1595=)
c.4755C= (p.Ala1585=)
c.4827C= (p.Ala1609=)
3g.38551488G>TCA433134282SCN5Ac.4881C>A (p.Ala1627=)
c.4884C>A (p.Ala1628=)
c.4830C>A (p.Ala1610=)
c.4722C>A (p.Ala1574=)
c.4785C>A (p.Ala1595=)
c.4755C>A (p.Ala1585=)
c.4827C>A (p.Ala1609=)
3g.38551489G>ACA352143029SCN5Ac.4880C>T (p.Ala1627Val)
c.4883C>T (p.Ala1628Val)
c.4829C>T (p.Ala1610Val)
c.4721C>T (p.Ala1574Val)
c.4784C>T (p.Ala1595Val)
c.4754C>T (p.Ala1585Val)
c.4826C>T (p.Ala1609Val)
3g.38551489G>CCA352143031SCN5Ac.4880C>G (p.Ala1627Gly)
c.4883C>G (p.Ala1628Gly)
c.4829C>G (p.Ala1610Gly)
c.4721C>G (p.Ala1574Gly)
c.4784C>G (p.Ala1595Gly)
c.4754C>G (p.Ala1585Gly)
c.4826C>G (p.Ala1609Gly)
3g.38551489G=CA1358558212SCN5Ac.4880C= (p.Ala1627=)
c.4883C= (p.Ala1628=)
c.4829C= (p.Ala1610=)
c.4721C= (p.Ala1574=)
c.4784C= (p.Ala1595=)
c.4754C= (p.Ala1585=)
c.4826C= (p.Ala1609=)
3g.38551489G>TCA352143030SCN5Ac.4880C>A (p.Ala1627Asp)
c.4883C>A (p.Ala1628Asp)
c.4829C>A (p.Ala1610Asp)
c.4721C>A (p.Ala1574Asp)
c.4784C>A (p.Ala1595Asp)
c.4754C>A (p.Ala1585Asp)
c.4826C>A (p.Ala1609Asp)
ClinVar dbSNP
3g.38551490C>ACA352143032SCN5Ac.4879G>T (p.Ala1627Ser)
c.4882G>T (p.Ala1628Ser)
c.4828G>T (p.Ala1610Ser)
c.4720G>T (p.Ala1574Ser)
c.4783G>T (p.Ala1595Ser)
c.4753G>T (p.Ala1585Ser)
c.4825G>T (p.Ala1609Ser)
3g.38551490C>GCA352143033SCN5Ac.4879G>C (p.Ala1627Pro)
c.4882G>C (p.Ala1628Pro)
c.4828G>C (p.Ala1610Pro)
c.4720G>C (p.Ala1574Pro)
c.4783G>C (p.Ala1595Pro)
c.4753G>C (p.Ala1585Pro)
c.4825G>C (p.Ala1609Pro)
3g.38551490C>TCA352143034SCN5Ac.4879G>A (p.Ala1627Thr)
c.4882G>A (p.Ala1628Thr)
c.4828G>A (p.Ala1610Thr)
c.4720G>A (p.Ala1574Thr)
c.4783G>A (p.Ala1595Thr)
c.4753G>A (p.Ala1585Thr)
c.4825G>A (p.Ala1609Thr)
3g.38551491C>ACA433134283SCN5Ac.4878G>T (p.Leu1626=)
c.4881G>T (p.Leu1627=)
c.4827G>T (p.Leu1609=)
c.4719G>T (p.Leu1573=)
c.4782G>T (p.Leu1594=)
c.4752G>T (p.Leu1584=)
c.4824G>T (p.Leu1608=)
3g.38551491C>GCA433134284SCN5Ac.4878G>C (p.Leu1626=)
c.4881G>C (p.Leu1627=)
c.4827G>C (p.Leu1609=)
c.4719G>C (p.Leu1573=)
c.4782G>C (p.Leu1594=)
c.4752G>C (p.Leu1584=)
c.4824G>C (p.Leu1608=)
3g.38551491C>TCA433134286SCN5Ac.4878G>A (p.Leu1626=)
c.4881G>A (p.Leu1627=)
c.4827G>A (p.Leu1609=)
c.4719G>A (p.Leu1573=)
c.4782G>A (p.Leu1594=)
c.4752G>A (p.Leu1584=)
c.4824G>A (p.Leu1608=)
ClinVar
3g.38551492A>CCA352143035SCN5Ac.4877T>G (p.Leu1626Arg)
c.4880T>G (p.Leu1627Arg)
c.4826T>G (p.Leu1609Arg)
c.4718T>G (p.Leu1573Arg)
c.4781T>G (p.Leu1594Arg)
c.4751T>G (p.Leu1584Arg)
c.4823T>G (p.Leu1608Arg)
3g.38551492A>GCA352143036SCN5Ac.4877T>C (p.Leu1626Pro)
c.4880T>C (p.Leu1627Pro)
c.4826T>C (p.Leu1609Pro)
c.4718T>C (p.Leu1573Pro)
c.4781T>C (p.Leu1594Pro)
c.4751T>C (p.Leu1584Pro)
c.4823T>C (p.Leu1608Pro)
3g.38551492A>TCA352143037SCN5Ac.4877T>A (p.Leu1626Gln)
c.4880T>A (p.Leu1627Gln)
c.4826T>A (p.Leu1609Gln)
c.4718T>A (p.Leu1573Gln)
c.4781T>A (p.Leu1594Gln)
c.4751T>A (p.Leu1584Gln)
c.4823T>A (p.Leu1608Gln)
3g.38551493G>ACA433134287SCN5Ac.4876C>T (p.Leu1626=)
c.4879C>T (p.Leu1627=)
c.4825C>T (p.Leu1609=)
c.4717C>T (p.Leu1573=)
c.4780C>T (p.Leu1594=)
c.4750C>T (p.Leu1584=)
c.4822C>T (p.Leu1608=)
3g.38551493G>CCA352143038SCN5Ac.4876C>G (p.Leu1626Val)
c.4879C>G (p.Leu1627Val)
c.4825C>G (p.Leu1609Val)
c.4717C>G (p.Leu1573Val)
c.4780C>G (p.Leu1594Val)
c.4750C>G (p.Leu1584Val)
c.4822C>G (p.Leu1608Val)
gnomAD v4
3g.38551493G>TCA352143039SCN5Ac.4876C>A (p.Leu1626Met)
c.4879C>A (p.Leu1627Met)
c.4825C>A (p.Leu1609Met)
c.4717C>A (p.Leu1573Met)
c.4780C>A (p.Leu1594Met)
c.4750C>A (p.Leu1584Met)
c.4822C>A (p.Leu1608Met)
3g.38551494delCA2586965832SCN5Ac.4876del (p.Leu1626TrpfsTer4)
c.4879del (p.Leu1627TrpfsTer4)
c.4825del (p.Leu1609TrpfsTer4)
c.4717del (p.Leu1573TrpfsTer4)
c.4780del (p.Leu1594TrpfsTer4)
c.4750del (p.Leu1584TrpfsTer4)
c.4822del (p.Leu1608TrpfsTer4)
3g.38551494G>ACA433134288SCN5Ac.4875C>T (p.Arg1625=)
c.4878C>T (p.Arg1626=)
c.4824C>T (p.Arg1608=)
c.4716C>T (p.Arg1572=)
c.4779C>T (p.Arg1593=)
c.4749C>T (p.Arg1583=)
c.4821C>T (p.Arg1607=)
3g.38551494G>CCA433134290SCN5Ac.4875C>G (p.Arg1625=)
c.4878C>G (p.Arg1626=)
c.4824C>G (p.Arg1608=)
c.4716C>G (p.Arg1572=)
c.4779C>G (p.Arg1593=)
c.4749C>G (p.Arg1583=)
c.4821C>G (p.Arg1607=)
3g.38551494G>TCA433134292SCN5Ac.4875C>A (p.Arg1625=)
c.4878C>A (p.Arg1626=)
c.4824C>A (p.Arg1608=)
c.4716C>A (p.Arg1572=)
c.4779C>A (p.Arg1593=)
c.4749C>A (p.Arg1583=)
c.4821C>A (p.Arg1607=)
3g.38551495C>ACA352143040SCN5Ac.4874G>T (p.Arg1625Leu)
c.4877G>T (p.Arg1626Leu)
c.4823G>T (p.Arg1608Leu)
c.4715G>T (p.Arg1572Leu)
c.4778G>T (p.Arg1593Leu)
c.4748G>T (p.Arg1583Leu)
c.4820G>T (p.Arg1607Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38551495C=CA1358558220SCN5Ac.4874G= (p.Arg1625=)
c.4877G= (p.Arg1626=)
c.4823G= (p.Arg1608=)
c.4715G= (p.Arg1572=)
c.4778G= (p.Arg1593=)
c.4748G= (p.Arg1583=)
c.4820G= (p.Arg1607=)
3g.38551495C>GCA018703SCN5Ac.4874G>C (p.Arg1625Pro)
c.4877G>C (p.Arg1626Pro)
c.4823G>C (p.Arg1608Pro)
c.4715G>C (p.Arg1572Pro)
c.4778G>C (p.Arg1593Pro)
c.4748G>C (p.Arg1583Pro)
c.4820G>C (p.Arg1607Pro)
ClinVar dbSNP
3g.38551495C>TCA018698SCN5Ac.4874G>A (p.Arg1625His)
c.4877G>A (p.Arg1626His)
c.4823G>A (p.Arg1608His)
c.4715G>A (p.Arg1572His)
c.4778G>A (p.Arg1593His)
c.4748G>A (p.Arg1583His)
c.4820G>A (p.Arg1607His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38551496G>ACA16611263SCN5Ac.4873C>T (p.Arg1625Cys)
c.4876C>T (p.Arg1626Cys)
c.4822C>T (p.Arg1608Cys)
c.4714C>T (p.Arg1572Cys)
c.4777C>T (p.Arg1593Cys)
c.4747C>T (p.Arg1583Cys)
c.4819C>T (p.Arg1607Cys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38551496G>CCA352143041SCN5Ac.4873C>G (p.Arg1625Gly)
c.4876C>G (p.Arg1626Gly)
c.4822C>G (p.Arg1608Gly)
c.4714C>G (p.Arg1572Gly)
c.4777C>G (p.Arg1593Gly)
c.4747C>G (p.Arg1583Gly)
c.4819C>G (p.Arg1607Gly)
3g.38551496G=CA1358558229SCN5Ac.4873C= (p.Arg1625=)
c.4876C= (p.Arg1626=)
c.4822C= (p.Arg1608=)
c.4714C= (p.Arg1572=)
c.4777C= (p.Arg1593=)
c.4747C= (p.Arg1583=)
c.4819C= (p.Arg1607=)
3g.38551496G>TCA352143042SCN5Ac.4873C>A (p.Arg1625Ser)
c.4876C>A (p.Arg1626Ser)
c.4822C>A (p.Arg1608Ser)
c.4714C>A (p.Arg1572Ser)
c.4777C>A (p.Arg1593Ser)
c.4747C>A (p.Arg1583Ser)
c.4819C>A (p.Arg1607Ser)
3g.38551497G>ACA433134295SCN5Ac.4872C>T (p.Ile1624=)
c.4875C>T (p.Ile1625=)
c.4821C>T (p.Ile1607=)
c.4713C>T (p.Ile1571=)
c.4776C>T (p.Ile1592=)
c.4746C>T (p.Ile1582=)
c.4818C>T (p.Ile1606=)
3g.38551497G>CCA352143043SCN5Ac.4872C>G (p.Ile1624Met)
c.4875C>G (p.Ile1625Met)
c.4821C>G (p.Ile1607Met)
c.4713C>G (p.Ile1571Met)
c.4776C>G (p.Ile1592Met)
c.4746C>G (p.Ile1582Met)
c.4818C>G (p.Ile1606Met)
3g.38551497G>TCA433134297SCN5Ac.4872C>A (p.Ile1624=)
c.4875C>A (p.Ile1625=)
c.4821C>A (p.Ile1607=)
c.4713C>A (p.Ile1571=)
c.4776C>A (p.Ile1592=)
c.4746C>A (p.Ile1582=)
c.4818C>A (p.Ile1606=)
3g.38551498A>CCA352143044SCN5Ac.4871T>G (p.Ile1624Ser)
c.4874T>G (p.Ile1625Ser)
c.4820T>G (p.Ile1607Ser)
c.4712T>G (p.Ile1571Ser)
c.4775T>G (p.Ile1592Ser)
c.4745T>G (p.Ile1582Ser)
c.4817T>G (p.Ile1606Ser)
3g.38551498A>GCA352143045SCN5Ac.4871T>C (p.Ile1624Thr)
c.4874T>C (p.Ile1625Thr)
c.4820T>C (p.Ile1607Thr)
c.4712T>C (p.Ile1571Thr)
c.4775T>C (p.Ile1592Thr)
c.4745T>C (p.Ile1582Thr)
c.4817T>C (p.Ile1606Thr)
3g.38551498A>TCA352143046SCN5Ac.4871T>A (p.Ile1624Asn)
c.4874T>A (p.Ile1625Asn)
c.4820T>A (p.Ile1607Asn)
c.4712T>A (p.Ile1571Asn)
c.4775T>A (p.Ile1592Asn)
c.4745T>A (p.Ile1582Asn)
c.4817T>A (p.Ile1606Asn)
3g.38551499T>ACA352143047SCN5Ac.4870A>T (p.Ile1624Phe)
c.4873A>T (p.Ile1625Phe)
c.4819A>T (p.Ile1607Phe)
c.4711A>T (p.Ile1571Phe)
c.4774A>T (p.Ile1592Phe)
c.4744A>T (p.Ile1582Phe)
c.4816A>T (p.Ile1606Phe)
3g.38551499T>CCA352143048SCN5Ac.4870A>G (p.Ile1624Val)
c.4873A>G (p.Ile1625Val)
c.4819A>G (p.Ile1607Val)
c.4711A>G (p.Ile1571Val)
c.4774A>G (p.Ile1592Val)
c.4744A>G (p.Ile1582Val)
c.4816A>G (p.Ile1606Val)
3g.38551499T>GCA352143049SCN5Ac.4870A>C (p.Ile1624Leu)
c.4873A>C (p.Ile1625Leu)
c.4819A>C (p.Ile1607Leu)
c.4711A>C (p.Ile1571Leu)
c.4774A>C (p.Ile1592Leu)
c.4744A>C (p.Ile1582Leu)
c.4816A>C (p.Ile1606Leu)
3g.38551500G>ACA433134299SCN5Ac.4869C>T (p.Val1623=)
c.4872C>T (p.Val1624=)
c.4818C>T (p.Val1606=)
c.4710C>T (p.Val1570=)
c.4773C>T (p.Val1591=)
c.4743C>T (p.Val1581=)
c.4815C>T (p.Val1605=)

Number of alleles fetched