Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38597878A=CA1358584147SCN5Ac.2113T= (p.Ser705=)
c.1984T= (p.Ser662=)
3g.38597878A>CCA352144743SCN5Ac.2113T>G (p.Ser705Ala)
c.1984T>G (p.Ser662Ala)
3g.38597878A>GCA352144744SCN5Ac.2113T>C (p.Ser705Pro)
c.1984T>C (p.Ser662Pro)
dbSNP gnomAD v2 gnomAD v4
3g.38597878A>TCA352144745SCN5Ac.2113T>A (p.Ser705Thr)
c.1984T>A (p.Ser662Thr)
3g.38597879C>ACA352144748SCN5Ac.2112G>T (p.Met704Ile)
c.1983G>T (p.Met661Ile)
3g.38597879C>GCA352144747SCN5Ac.2112G>C (p.Met704Ile)
c.1983G>C (p.Met661Ile)
3g.38597879C>TCA352144746SCN5Ac.2112G>A (p.Met704Ile)
c.1983G>A (p.Met661Ile)
gnomAD v4
3g.38597880A>CCA352144749SCN5Ac.2111T>G (p.Met704Arg)
c.1982T>G (p.Met661Arg)
3g.38597880A>GCA352144750SCN5Ac.2111T>C (p.Met704Thr)
c.1982T>C (p.Met661Thr)
3g.38597880A>TCA352144751SCN5Ac.2111T>A (p.Met704Lys)
c.1982T>A (p.Met661Lys)
3g.38597881T>ACA352144752SCN5Ac.2110A>T (p.Met704Leu)
c.1981A>T (p.Met661Leu)
3g.38597881T>CCA352144753SCN5Ac.2110A>G (p.Met704Val)
c.1981A>G (p.Met661Val)
3g.38597881T>GCA352144754SCN5Ac.2110A>C (p.Met704Leu)
c.1981A>C (p.Met661Leu)
3g.38597882C>ACA352144755SCN5Ac.2109G>T (p.Trp703Cys)
c.1980G>T (p.Trp660Cys)
3g.38597882C=CA1358584151SCN5Ac.2109G= (p.Trp703=)
c.1980G= (p.Trp660=)
3g.38597882C>GCA352144756SCN5Ac.2109G>C (p.Trp703Cys)
c.1980G>C (p.Trp660Cys)
3g.38597882C>TCA352144757SCN5Ac.2109G>A (p.Trp703Ter)
c.1980G>A (p.Trp660Ter)
dbSNP
3g.38597883C>ACA352144758SCN5Ac.2108G>T (p.Trp703Leu)
c.1979G>T (p.Trp660Leu)
3g.38597883C>GCA352144759SCN5Ac.2108G>C (p.Trp703Ser)
c.1979G>C (p.Trp660Ser)
3g.38597883C>TCA352144760SCN5Ac.2108G>A (p.Trp703Ter)
c.1979G>A (p.Trp660Ter)
gnomAD v4
3g.38597884A>CCA352144762SCN5Ac.2107T>G (p.Trp703Gly)
c.1978T>G (p.Trp660Gly)
3g.38597884A>GCA352144763SCN5Ac.2107T>C (p.Trp703Arg)
c.1978T>C (p.Trp660Arg)
gnomAD v4
3g.38597884A>TCA352144761SCN5Ac.2107T>A (p.Trp703Arg)
c.1978T>A (p.Trp660Arg)
3g.38597885C>ACA433333140SCN5Ac.2106G>T (p.Leu702=)
c.1977G>T (p.Leu659=)
3g.38597885C=CA1358584154SCN5Ac.2106G= (p.Leu702=)
c.1977G= (p.Leu659=)
3g.38597885C>GCA433333141SCN5Ac.2106G>C (p.Leu702=)
c.1977G>C (p.Leu659=)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38597885C>TCA433333139SCN5Ac.2106G>A (p.Leu702=)
c.1977G>A (p.Leu659=)
ClinVar dbSNP gnomAD v4
3g.38597886A>CCA352144766SCN5Ac.2105T>G (p.Leu702Arg)
c.1976T>G (p.Leu659Arg)
3g.38597886A>GCA352144764SCN5Ac.2105T>C (p.Leu702Pro)
c.1976T>C (p.Leu659Pro)
3g.38597886A>TCA352144765SCN5Ac.2105T>A (p.Leu702Gln)
c.1976T>A (p.Leu659Gln)
3g.38597887G>ACA433333142SCN5Ac.2104C>T (p.Leu702=)
c.1975C>T (p.Leu659=)
gnomAD v4
3g.38597887G>CCA352144767SCN5Ac.2104C>G (p.Leu702Val)
c.1975C>G (p.Leu659Val)
3g.38597887G>TCA352144768SCN5Ac.2104C>A (p.Leu702Met)
c.1975C>A (p.Leu659Met)
3g.38597887_38597888delinsGCCA1358584159SCN5Ac.2103_2104delinsGC (p.Pro701=)
c.1974_1975delinsGC (p.Pro658=)
3g.38597888delCA015846SCN5Ac.2103del (p.Leu702CysfsTer9)
c.1974del (p.Leu659CysfsTer9)
ClinVar dbSNP
3g.38597888C>ACA433333146SCN5Ac.2103G>T (p.Pro701=)
c.1974G>T (p.Pro658=)
ClinVar dbSNP gnomAD v4
3g.38597888C=CA1358584164SCN5Ac.2103G= (p.Pro701=)
c.1974G= (p.Pro658=)
3g.38597888C>GCA433333147SCN5Ac.2103G>C (p.Pro701=)
c.1974G>C (p.Pro658=)
3g.38597888C>TCA059789SCN5Ac.2103G>A (p.Pro701=)
c.1974G>A (p.Pro658=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38597889G>ACA015838SCN5Ac.2102C>T (p.Pro701Leu)
c.1973C>T (p.Pro658Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38597889G>CCA352144769SCN5Ac.2102C>G (p.Pro701Arg)
c.1973C>G (p.Pro658Arg)
3g.38597889G=CA1358584171SCN5Ac.2102C= (p.Pro701=)
c.1973C= (p.Pro658=)
3g.38597889G>TCA352144770SCN5Ac.2102C>A (p.Pro701Gln)
c.1973C>A (p.Pro658Gln)
dbSNP
3g.38597891delCA2586971900SCN5Ac.2102del (p.Pro701ArgfsTer10)
c.1973del (p.Pro658ArgfsTer10)
3g.38597890G>ACA352144771SCN5Ac.2101C>T (p.Pro701Ser)
c.1972C>T (p.Pro658Ser)
3g.38597890G>CCA352144772SCN5Ac.2101C>G (p.Pro701Ala)
c.1972C>G (p.Pro658Ala)
3g.38597890G>TCA352144773SCN5Ac.2101C>A (p.Pro701Thr)
c.1972C>A (p.Pro658Thr)
3g.38597891G>ACA433333149SCN5Ac.2100C>T (p.Cys700=)
c.1971C>T (p.Cys657=)
gnomAD v4
3g.38597891G>CCA352144774SCN5Ac.2100C>G (p.Cys700Trp)
c.1971C>G (p.Cys657Trp)
3g.38597891G=CA1358584175SCN5Ac.2100C= (p.Cys700=)
c.1971C= (p.Cys657=)
3g.38597891G>TCA352144775SCN5Ac.2100C>A (p.Cys700Ter)
c.1971C>A (p.Cys657Ter)
dbSNP
3g.38597892C>ACA352144776SCN5Ac.2099G>T (p.Cys700Phe)
c.1970G>T (p.Cys657Phe)
3g.38597892C>GCA352144778SCN5Ac.2099G>C (p.Cys700Ser)
c.1970G>C (p.Cys657Ser)
3g.38597892C>TCA352144777SCN5Ac.2099G>A (p.Cys700Tyr)
c.1970G>A (p.Cys657Tyr)
gnomAD v4
3g.38597893A>CCA352144779SCN5Ac.2098T>G (p.Cys700Gly)
c.1969T>G (p.Cys657Gly)
3g.38597893A>GCA352144780SCN5Ac.2098T>C (p.Cys700Arg)
c.1969T>C (p.Cys657Arg)
3g.38597893A>TCA352144781SCN5Ac.2098T>A (p.Cys700Ser)
c.1969T>A (p.Cys657Ser)
3g.38597894G>ACA433333151SCN5Ac.2097C>T (p.Cys699=)
c.1968C>T (p.Cys656=)
3g.38597894G>CCA352144782SCN5Ac.2097C>G (p.Cys699Trp)
c.1968C>G (p.Cys656Trp)
3g.38597894G=CA1358584178SCN5Ac.2097C= (p.Cys699=)
c.1968C= (p.Cys656=)
3g.38597894G>TCA352144783SCN5Ac.2097C>A (p.Cys699Ter)
c.1968C>A (p.Cys656Ter)
dbSNP
3g.38597895C>ACA352144784SCN5Ac.2096G>T (p.Cys699Phe)
c.1967G>T (p.Cys656Phe)
3g.38597895C>GCA352144785SCN5Ac.2096G>C (p.Cys699Ser)
c.1967G>C (p.Cys656Ser)
3g.38597895C>TCA352144786SCN5Ac.2096G>A (p.Cys699Tyr)
c.1967G>A (p.Cys656Tyr)
3g.38597896A>CCA352144787SCN5Ac.2095T>G (p.Cys699Gly)
c.1966T>G (p.Cys656Gly)
gnomAD v4
3g.38597896A>GCA352144788SCN5Ac.2095T>C (p.Cys699Arg)
c.1966T>C (p.Cys656Arg)
gnomAD v4
3g.38597896A>TCA352144789SCN5Ac.2095T>A (p.Cys699Ser)
c.1966T>A (p.Cys656Ser)
3g.38597897C>ACA352144790SCN5Ac.2094G>T (p.Glu698Asp)
c.1965G>T (p.Glu655Asp)
3g.38597897C=CA1358584181SCN5Ac.2094G= (p.Glu698=)
c.1965G= (p.Glu655=)
3g.38597897C>GCA352144791SCN5Ac.2094G>C (p.Glu698Asp)
c.1965G>C (p.Glu655Asp)
3g.38597897C>TCA433333155SCN5Ac.2094G>A (p.Glu698=)
c.1965G>A (p.Glu655=)
ClinVar dbSNP gnomAD v4
3g.38597898T>ACA352144792SCN5Ac.2093A>T (p.Glu698Val)
c.1964A>T (p.Glu655Val)
3g.38597898T>CCA352144793SCN5Ac.2093A>G (p.Glu698Gly)
c.1964A>G (p.Glu655Gly)
3g.38597898T>GCA352144794SCN5Ac.2093A>C (p.Glu698Ala)
c.1964A>C (p.Glu655Ala)
3g.38597899C>ACA352144795SCN5Ac.2092G>T (p.Glu698Ter)
c.1963G>T (p.Glu655Ter)
dbSNP
3g.38597899C=CA1358584186SCN5Ac.2092G= (p.Glu698=)
c.1963G= (p.Glu655=)
3g.38597899C>GCA352144796SCN5Ac.2092G>C (p.Glu698Gln)
c.1963G>C (p.Glu655Gln)
3g.38597899C>TCA352144797SCN5Ac.2092G>A (p.Glu698Lys)
c.1963G>A (p.Glu655Lys)
COSMIC COSMIC COSMIC
3g.38597900C>ACA352144798SCN5Ac.2091G>T (p.Trp697Cys)
c.1962G>T (p.Trp654Cys)
3g.38597900C=CA1358584190SCN5Ac.2091G= (p.Trp697=)
c.1962G= (p.Trp654=)
3g.38597900C>GCA352144799SCN5Ac.2091G>C (p.Trp697Cys)
c.1962G>C (p.Trp654Cys)
3g.38597900C>TCA352144800SCN5Ac.2091G>A (p.Trp697Ter)
c.1962G>A (p.Trp654Ter)
ClinVar dbSNP
3g.38597901C>ACA352144801SCN5Ac.2090G>T (p.Trp697Leu)
c.1961G>T (p.Trp654Leu)
3g.38597901C>GCA352144802SCN5Ac.2090G>C (p.Trp697Ser)
c.1961G>C (p.Trp654Ser)
3g.38597901C>TCA352144803SCN5Ac.2090G>A (p.Trp697Ter)
c.1961G>A (p.Trp654Ter)
3g.38597902A>CCA352144806SCN5Ac.2089T>G (p.Trp697Gly)
c.1960T>G (p.Trp654Gly)
3g.38597902A>GCA352144805SCN5Ac.2089T>C (p.Trp697Arg)
c.1960T>C (p.Trp654Arg)
3g.38597902A>TCA352144804SCN5Ac.2089T>A (p.Trp697Arg)
c.1960T>A (p.Trp654Arg)
3g.38597903G>ACA433333160SCN5Ac.2088C>T (p.Ile696=)
c.1959C>T (p.Ile653=)
3g.38597903G>CCA352144807SCN5Ac.2088C>G (p.Ile696Met)
c.1959C>G (p.Ile653Met)
3g.38597903G>TCA433333161SCN5Ac.2088C>A (p.Ile696=)
c.1959C>A (p.Ile653=)
3g.38597904A=CA1358584192SCN5Ac.2087T= (p.Ile696=)
c.1958T= (p.Ile653=)
3g.38597904A>CCA352144808SCN5Ac.2087T>G (p.Ile696Ser)
c.1958T>G (p.Ile653Ser)
3g.38597904A>GCA352144809SCN5Ac.2087T>C (p.Ile696Thr)
c.1958T>C (p.Ile653Thr)
3g.38597904A>TCA72932583SCN5Ac.2087T>A (p.Ile696Asn)
c.1958T>A (p.Ile653Asn)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38597905T>ACA352144810SCN5Ac.2086A>T (p.Ile696Phe)
c.1957A>T (p.Ile653Phe)
3g.38597905T>CCA352144811SCN5Ac.2086A>G (p.Ile696Val)
c.1957A>G (p.Ile653Val)
gnomAD v4
3g.38597905T>GCA352144812SCN5Ac.2086A>C (p.Ile696Leu)
c.1957A>C (p.Ile653Leu)
3g.38597906C>ACA433333168SCN5Ac.2085G>T (p.Leu695=)
c.1956G>T (p.Leu652=)
3g.38597906C=CA1358584198SCN5Ac.2085G= (p.Leu695=)
c.1956G= (p.Leu652=)
3g.38597906C>GCA433333167SCN5Ac.2085G>C (p.Leu695=)
c.1956G>C (p.Leu652=)
3g.38597906C>TCA059749SCN5Ac.2085G>A (p.Leu695=)
c.1956G>A (p.Leu652=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38597907A>CCA352144813SCN5Ac.2084T>G (p.Leu695Arg)
c.1955T>G (p.Leu652Arg)
3g.38597907A>GCA352144814SCN5Ac.2084T>C (p.Leu695Pro)
c.1955T>C (p.Leu652Pro)
3g.38597907A>TCA352144815SCN5Ac.2084T>A (p.Leu695Gln)
c.1955T>A (p.Leu652Gln)
3g.38597908G>ACA433333170SCN5Ac.2083C>T (p.Leu695=)
c.1954C>T (p.Leu652=)
3g.38597908G>CCA352144816SCN5Ac.2083C>G (p.Leu695Val)
c.1954C>G (p.Leu652Val)
3g.38597908G>TCA352144817SCN5Ac.2083C>A (p.Leu695Met)
c.1954C>A (p.Leu652Met)
3g.38597909G>ACA059737SCN5Ac.2082C>T (p.Tyr694=)
c.1953C>T (p.Tyr651=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38597909G>CCA352144819SCN5Ac.2082C>G (p.Tyr694Ter)
c.1953C>G (p.Tyr651Ter)
3g.38597909G=CA1358584202SCN5Ac.2082C= (p.Tyr694=)
c.1953C= (p.Tyr651=)
3g.38597909G>TCA352144818SCN5Ac.2082C>A (p.Tyr694Ter)
c.1953C>A (p.Tyr651Ter)
ClinVar
3g.38597910T>ACA352144820SCN5Ac.2081A>T (p.Tyr694Phe)
c.1952A>T (p.Tyr651Phe)
3g.38597910T>CCA352144821SCN5Ac.2081A>G (p.Tyr694Cys)
c.1952A>G (p.Tyr651Cys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38597910T>GCA352144822SCN5Ac.2081A>C (p.Tyr694Ser)
c.1952A>C (p.Tyr651Ser)
3g.38597910T=CA1358584207SCN5Ac.2081A= (p.Tyr694=)
c.1952A= (p.Tyr651=)
3g.38597911A>CCA352144823SCN5Ac.2080T>G (p.Tyr694Asp)
c.1951T>G (p.Tyr651Asp)
3g.38597911A>GCA352144824SCN5Ac.2080T>C (p.Tyr694His)
c.1951T>C (p.Tyr651His)
3g.38597911A>TCA352144825SCN5Ac.2080T>A (p.Tyr694Asn)
c.1951T>A (p.Tyr651Asn)
3g.38597912G>ACA433333182SCN5Ac.2079C>T (p.Arg693=)
c.1950C>T (p.Arg650=)
3g.38597912G>CCA433333184SCN5Ac.2079C>G (p.Arg693=)
c.1950C>G (p.Arg650=)
3g.38597912G>TCA433333183SCN5Ac.2079C>A (p.Arg693=)
c.1950C>A (p.Arg650=)
3g.38597913C>ACA352144827SCN5Ac.2078G>T (p.Arg693Leu)
c.1949G>T (p.Arg650Leu)
ClinVar dbSNP gnomAD v4
3g.38597913C=CA1358584212SCN5Ac.2078G= (p.Arg693=)
c.1949G= (p.Arg650=)
3g.38597913C>GCA352144826SCN5Ac.2078G>C (p.Arg693Pro)
c.1949G>C (p.Arg650Pro)
3g.38597913C>TCA059728SCN5Ac.2078G>A (p.Arg693His)
c.1949G>A (p.Arg650His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38597914G>ACA059716SCN5Ac.2077C>T (p.Arg693Cys)
c.1948C>T (p.Arg650Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38597914G>CCA352144828SCN5Ac.2077C>G (p.Arg693Gly)
c.1948C>G (p.Arg650Gly)
gnomAD v4
3g.38597914G=CA1358584215SCN5Ac.2077C= (p.Arg693=)
c.1948C= (p.Arg650=)
3g.38597914G>TCA352144829SCN5Ac.2077C>A (p.Arg693Ser)
c.1948C>A (p.Arg650Ser)
3g.38597915C>ACA352144830SCN5Ac.2076G>T (p.Gln692His)
c.1947G>T (p.Gln649His)
ClinVar dbSNP
3g.38597915C=CA1358584220SCN5Ac.2076G= (p.Gln692=)
c.1947G= (p.Gln649=)
3g.38597915C>GCA352144831SCN5Ac.2076G>C (p.Gln692His)
c.1947G>C (p.Gln649His)
3g.38597915C>TCA433333194SCN5Ac.2076G>A (p.Gln692=)
c.1947G>A (p.Gln649=)
3g.38597916T>ACA352144834SCN5Ac.2075A>T (p.Gln692Leu)
c.1946A>T (p.Gln649Leu)
3g.38597916T>CCA352144832SCN5Ac.2075A>G (p.Gln692Arg)
c.1946A>G (p.Gln649Arg)
3g.38597916T>GCA352144833SCN5Ac.2075A>C (p.Gln692Pro)
c.1946A>C (p.Gln649Pro)
dbSNP gnomAD v4
3g.38597916T=CA1358584223SCN5Ac.2075A= (p.Gln692=)
c.1946A= (p.Gln649=)
3g.38597917G>ACA352144835SCN5Ac.2074C>T (p.Gln692Ter)
c.1945C>T (p.Gln649Ter)
3g.38597917G>CCA352144836SCN5Ac.2074C>G (p.Gln692Glu)
c.1945C>G (p.Gln649Glu)
3g.38597917G=CA1358584228SCN5Ac.2074C= (p.Gln692=)
c.1945C= (p.Gln649=)
3g.38597917G>TCA015830SCN5Ac.2074C>A (p.Gln692Lys)
c.1945C>A (p.Gln649Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38597918G>ACA433333201SCN5Ac.2073C>T (p.Ala691=)
c.1944C>T (p.Ala648=)
3g.38597918G>CCA433333202SCN5Ac.2073C>G (p.Ala691=)
c.1944C>G (p.Ala648=)
3g.38597918G>TCA433333203SCN5Ac.2073C>A (p.Ala691=)
c.1944C>A (p.Ala648=)
ClinVar
3g.38597919G>ACA352144837SCN5Ac.2072C>T (p.Ala691Val)
c.1943C>T (p.Ala648Val)
dbSNP gnomAD v4
3g.38597919G>CCA352144838SCN5Ac.2072C>G (p.Ala691Gly)
c.1943C>G (p.Ala648Gly)
3g.38597919G=CA1358584231SCN5Ac.2072C= (p.Ala691=)
c.1943C= (p.Ala648=)
3g.38597919G>TCA352144839SCN5Ac.2072C>A (p.Ala691Asp)
c.1943C>A (p.Ala648Asp)
dbSNP
3g.38597920C>ACA059697SCN5Ac.2071G>T (p.Ala691Ser)
c.1942G>T (p.Ala648Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38597920C=CA1358584237SCN5Ac.2071G= (p.Ala691=)
c.1942G= (p.Ala648=)
3g.38597920C>GCA352144840SCN5Ac.2071G>C (p.Ala691Pro)
c.1942G>C (p.Ala648Pro)
3g.38597920C>TCA015822SCN5Ac.2071G>A (p.Ala691Thr)
c.1942G>A (p.Ala648Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38597921G>ACA059681SCN5Ac.2070C>T (p.Leu690=)
c.1941C>T (p.Leu647=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38597921G>CCA433333215SCN5Ac.2070C>G (p.Leu690=)
c.1941C>G (p.Leu647=)
dbSNP gnomAD v4
3g.38597921G=CA1358584240SCN5Ac.2070C= (p.Leu690=)
c.1941C= (p.Leu647=)
3g.38597921G>TCA433333216SCN5Ac.2070C>A (p.Leu690=)
c.1941C>A (p.Leu647=)
3g.38597922A>CCA352144841SCN5Ac.2069T>G (p.Leu690Arg)
c.1940T>G (p.Leu647Arg)
3g.38597922A>GCA352144842SCN5Ac.2069T>C (p.Leu690Pro)
c.1940T>C (p.Leu647Pro)
3g.38597922A>TCA352144843SCN5Ac.2069T>A (p.Leu690His)
c.1940T>A (p.Leu647His)
3g.38597923G>ACA352144844SCN5Ac.2068C>T (p.Leu690Phe)
c.1939C>T (p.Leu647Phe)
3g.38597923G>CCA352144846SCN5Ac.2068C>G (p.Leu690Val)
c.1939C>G (p.Leu647Val)
3g.38597923G>TCA352144845SCN5Ac.2068C>A (p.Leu690Ile)
c.1939C>A (p.Leu647Ile)
3g.38597924A>CCA433333220SCN5Ac.2067T>G (p.Arg689=)
c.1938T>G (p.Arg646=)
3g.38597924A>GCA433333222SCN5Ac.2067T>C (p.Arg689=)
c.1938T>C (p.Arg646=)
3g.38597924A>TCA433333221SCN5Ac.2067T>A (p.Arg689=)
c.1938T>A (p.Arg646=)
3g.38597925C>ACA352144847SCN5Ac.2066G>T (p.Arg689Leu)
c.1937G>T (p.Arg646Leu)
3g.38597925C=CA1358584241SCN5Ac.2066G= (p.Arg689=)
c.1937G= (p.Arg646=)
3g.38597925C>GCA352144848SCN5Ac.2066G>C (p.Arg689Pro)
c.1937G>C (p.Arg646Pro)
ClinVar gnomAD v4
3g.38597925C>TCA015813SCN5Ac.2066G>A (p.Arg689His)
c.1937G>A (p.Arg646His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38597926G>ACA015805SCN5Ac.2065C>T (p.Arg689Cys)
c.1936C>T (p.Arg646Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38597926G>CCA352144849SCN5Ac.2065C>G (p.Arg689Gly)
c.1936C>G (p.Arg646Gly)
3g.38597926G=CA1358584242SCN5Ac.2065C= (p.Arg689=)
c.1936C= (p.Arg646=)
3g.38597926G>TCA352144850SCN5Ac.2065C>A (p.Arg689Ser)
c.1936C>A (p.Arg646Ser)
3g.38597927G>ACA433333231SCN5Ac.2064C>T (p.Asn688=)
c.1935C>T (p.Asn645=)
ClinVar
3g.38597927G>CCA352144852SCN5Ac.2064C>G (p.Asn688Lys)
c.1935C>G (p.Asn645Lys)
3g.38597927G>TCA352144851SCN5Ac.2064C>A (p.Asn688Lys)
c.1935C>A (p.Asn645Lys)
3g.38597928T>ACA352144853SCN5Ac.2063A>T (p.Asn688Ile)
c.1934A>T (p.Asn645Ile)
3g.38597928T>CCA352144854SCN5Ac.2063A>G (p.Asn688Ser)
c.1934A>G (p.Asn645Ser)
3g.38597928T>GCA352144855SCN5Ac.2063A>C (p.Asn688Thr)
c.1934A>C (p.Asn645Thr)
3g.38597929T>ACA352144856SCN5Ac.2062A>T (p.Asn688Tyr)
c.1933A>T (p.Asn645Tyr)
3g.38597929T>CCA352144857SCN5Ac.2062A>G (p.Asn688Asp)
c.1933A>G (p.Asn645Asp)
3g.38597929T>GCA352144858SCN5Ac.2062A>C (p.Asn688His)
c.1933A>C (p.Asn645His)
3g.38597930C>ACA352144859SCN5Ac.2061G>T (p.Trp687Cys)
c.1932G>T (p.Trp644Cys)
3g.38597930C=CA1358584245SCN5Ac.2061G= (p.Trp687=)
c.1932G= (p.Trp644=)
3g.38597930C>GCA352144861SCN5Ac.2061G>C (p.Trp687Cys)
c.1932G>C (p.Trp644Cys)
3g.38597930C>TCA352144860SCN5Ac.2061G>A (p.Trp687Ter)
c.1932G>A (p.Trp644Ter)
dbSNP COSMIC COSMIC COSMIC
3g.38597931C>ACA352144862SCN5Ac.2060G>T (p.Trp687Leu)
c.1931G>T (p.Trp644Leu)
3g.38597931C=CA1358584246SCN5Ac.2060G= (p.Trp687=)
c.1931G= (p.Trp644=)
3g.38597931C>GCA352144863SCN5Ac.2060G>C (p.Trp687Ser)
c.1931G>C (p.Trp644Ser)
3g.38597931C>TCA352144864SCN5Ac.2060G>A (p.Trp687Ter)
c.1931G>A (p.Trp644Ter)
3g.38597932A>CCA352144865SCN5Ac.2059T>G (p.Trp687Gly)
c.1930T>G (p.Trp644Gly)
3g.38597932A>GCA352144866SCN5Ac.2059T>C (p.Trp687Arg)
c.1930T>C (p.Trp644Arg)
3g.38597932A>TCA352144867SCN5Ac.2059T>A (p.Trp687Arg)
c.1930T>A (p.Trp644Arg)
3g.38597932dupCA1047009403SCN5Ac.2059dup (p.Trp687LeufsTer?)
c.1930dup (p.Trp644LeufsTer?)
dbSNP gnomAD v3 gnomAD v4
3g.38597933G>ACA433333247SCN5Ac.2058C>T (p.Cys686=)
c.1929C>T (p.Cys643=)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38597933G>CCA352144868SCN5Ac.2058C>G (p.Cys686Trp)
c.1929C>G (p.Cys643Trp)
3g.38597933G=CA1358584247SCN5Ac.2058C= (p.Cys686=)
c.1929C= (p.Cys643=)
3g.38597933G>TCA352144869SCN5Ac.2058C>A (p.Cys686Ter)
c.1929C>A (p.Cys643Ter)
dbSNP
3g.38597934C>ACA352144870SCN5Ac.2057G>T (p.Cys686Phe)
c.1928G>T (p.Cys643Phe)
dbSNP gnomAD v2 gnomAD v4
3g.38597934C=CA1358584251SCN5Ac.2057G= (p.Cys686=)
c.1928G= (p.Cys643=)
3g.38597934C>GCA352144871SCN5Ac.2057G>C (p.Cys686Ser)
c.1928G>C (p.Cys643Ser)
3g.38597934C>TCA352144872SCN5Ac.2057G>A (p.Cys686Tyr)
c.1928G>A (p.Cys643Tyr)
gnomAD v4
3g.38597935A>CCA352144873SCN5Ac.2056T>G (p.Cys686Gly)
c.1927T>G (p.Cys643Gly)
3g.38597935A>GCA352144875SCN5Ac.2056T>C (p.Cys686Arg)
c.1927T>C (p.Cys643Arg)
3g.38597935A>TCA352144874SCN5Ac.2056T>A (p.Cys686Ser)
c.1927T>A (p.Cys643Ser)
3g.38597936T>ACA433333251SCN5Ac.2055A>T (p.Pro685=)
c.1926A>T (p.Pro642=)
3g.38597936T>CCA433333252SCN5Ac.2055A>G (p.Pro685=)
c.1926A>G (p.Pro642=)
ClinVar dbSNP gnomAD v4
3g.38597936T>GCA433333253SCN5Ac.2055A>C (p.Pro685=)
c.1926A>C (p.Pro642=)
ClinVar dbSNP gnomAD v4
3g.38597937G>ACA352144876SCN5Ac.2054C>T (p.Pro685Leu)
c.1925C>T (p.Pro642Leu)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38597937G>CCA352144878SCN5Ac.2054C>G (p.Pro685Arg)
c.1925C>G (p.Pro642Arg)
3g.38597937G=CA1358584255SCN5Ac.2054C= (p.Pro685=)
c.1925C= (p.Pro642=)
3g.38597937G>TCA352144877SCN5Ac.2054C>A (p.Pro685Gln)
c.1925C>A (p.Pro642Gln)
3g.38597938G>ACA352144879SCN5Ac.2053C>T (p.Pro685Ser)
c.1924C>T (p.Pro642Ser)
dbSNP
3g.38597938G>CCA352144880SCN5Ac.2053C>G (p.Pro685Ala)
c.1924C>G (p.Pro642Ala)
3g.38597938G=CA1358584260SCN5Ac.2053C= (p.Pro685=)
c.1924C= (p.Pro642=)
3g.38597938G>TCA352144881SCN5Ac.2053C>A (p.Pro685Thr)
c.1924C>A (p.Pro642Thr)
gnomAD v4
3g.38597939T>ACA433333261SCN5Ac.2052A>T (p.Pro684=)
c.1923A>T (p.Pro641=)
ClinVar dbSNP
3g.38597939T>CCA059640SCN5Ac.2052A>G (p.Pro684=)
c.1923A>G (p.Pro641=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38597939T>GCA433333265SCN5Ac.2052A>C (p.Pro684=)
c.1923A>C (p.Pro641=)
gnomAD v4
3g.38597939T=CA1358584263SCN5Ac.2052A= (p.Pro684=)
c.1923A= (p.Pro641=)
3g.38597940G>ACA352144882SCN5Ac.2051C>T (p.Pro684Leu)
c.1922C>T (p.Pro641Leu)
3g.38597940G>CCA352144883SCN5Ac.2051C>G (p.Pro684Arg)
c.1922C>G (p.Pro641Arg)
3g.38597940G>TCA352144884SCN5Ac.2051C>A (p.Pro684Gln)
c.1922C>A (p.Pro641Gln)
3g.38597941G>ACA352144885SCN5Ac.2050C>T (p.Pro684Ser)
c.1921C>T (p.Pro641Ser)
3g.38597941G>CCA352144886SCN5Ac.2050C>G (p.Pro684Ala)
c.1921C>G (p.Pro641Ala)
3g.38597941G>TCA352144887SCN5Ac.2050C>A (p.Pro684Thr)
c.1921C>A (p.Pro641Thr)
3g.38597942A=CA1358584272SCN5Ac.2049T= (p.Cys683=)
c.1920T= (p.Cys640=)
3g.38597942A>CCA352144888SCN5Ac.2049T>G (p.Cys683Trp)
c.1920T>G (p.Cys640Trp)
3g.38597942A>GCA433333270SCN5Ac.2049T>C (p.Cys683=)
c.1920T>C (p.Cys640=)
3g.38597942A>TCA352144889SCN5Ac.2049T>A (p.Cys683Ter)
c.1920T>A (p.Cys640Ter)
dbSNP
3g.38597943C>ACA352144891SCN5Ac.2048G>T (p.Cys683Phe)
c.1919G>T (p.Cys640Phe)
3g.38597943C=CA1358584279SCN5Ac.2048G= (p.Cys683=)
c.1919G= (p.Cys640=)
3g.38597943C>GCA015794SCN5Ac.2048G>C (p.Cys683Ser)
c.1919G>C (p.Cys640Ser)
ClinVar dbSNP
3g.38597943C>TCA352144890SCN5Ac.2048G>A (p.Cys683Tyr)
c.1919G>A (p.Cys640Tyr)
ClinVar
3g.38597944A=CA1358584288SCN5Ac.2047T= (p.Cys683=)
c.1918T= (p.Cys640=)
3g.38597944A>CCA015785SCN5Ac.2047T>G (p.Cys683Gly)
c.1918T>G (p.Cys640Gly)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38597944A>GCA015776SCN5Ac.2047T>C (p.Cys683Arg)
c.1918T>C (p.Cys640Arg)
ClinVar dbSNP
3g.38597944A>TCA352144892SCN5Ac.2047T>A (p.Cys683Ser)
c.1918T>A (p.Cys640Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38597945C>ACA352144893SCN5Ac.2046G>T (p.Lys682Asn)
c.1917G>T (p.Lys639Asn)
3g.38597945C>GCA352144894SCN5Ac.2046G>C (p.Lys682Asn)
c.1917G>C (p.Lys639Asn)
3g.38597945C>TCA433333280SCN5Ac.2046G>A (p.Lys682=)
c.1917G>A (p.Lys639=)
3g.38597946T>ACA352144895SCN5Ac.2045A>T (p.Lys682Met)
c.1916A>T (p.Lys639Met)
3g.38597946T>CCA352144896SCN5Ac.2045A>G (p.Lys682Arg)
c.1916A>G (p.Lys639Arg)
3g.38597946T>GCA352144897SCN5Ac.2045A>C (p.Lys682Thr)
c.1916A>C (p.Lys639Thr)
dbSNP gnomAD v3 gnomAD v4
3g.38597946T=CA1358584296SCN5Ac.2045A= (p.Lys682=)
c.1916A= (p.Lys639=)
3g.38597947T>ACA352144898SCN5Ac.2044A>T (p.Lys682Ter)
c.1915A>T (p.Lys639Ter)
dbSNP
3g.38597947T>CCA352144899SCN5Ac.2044A>G (p.Lys682Glu)
c.1915A>G (p.Lys639Glu)
ClinVar
3g.38597947T>GCA352144900SCN5Ac.2044A>C (p.Lys682Gln)
c.1915A>C (p.Lys639Gln)
3g.38597947T=CA1358584298SCN5Ac.2044A= (p.Lys682=)
c.1915A= (p.Lys639=)
3g.38597948G>ACA433333283SCN5Ac.2043C>T (p.His681=)
c.1914C>T (p.His638=)
3g.38597948G>CCA352144902SCN5Ac.2043C>G (p.His681Gln)
c.1914C>G (p.His638Gln)
3g.38597948G>TCA352144901SCN5Ac.2043C>A (p.His681Gln)
c.1914C>A (p.His638Gln)
3g.38597949T>ACA352144903SCN5Ac.2042A>T (p.His681Leu)
c.1913A>T (p.His638Leu)
3g.38597949T>CCA352144904SCN5Ac.2042A>G (p.His681Arg)
c.1913A>G (p.His638Arg)
dbSNP gnomAD v4
3g.38597949T>GCA015766SCN5Ac.2042A>C (p.His681Pro)
c.1913A>C (p.His638Pro)
ClinVar dbSNP
3g.38597949T=CA1358584304SCN5Ac.2042A= (p.His681=)
c.1913A= (p.His638=)
3g.38597950G>ACA352144905SCN5Ac.2041C>T (p.His681Tyr)
c.1912C>T (p.His638Tyr)
3g.38597950G>CCA352144906SCN5Ac.2041C>G (p.His681Asp)
c.1912C>G (p.His638Asp)
dbSNP
3g.38597950G=CA1358584308SCN5Ac.2041C= (p.His681=)
c.1912C= (p.His638=)
3g.38597950G>TCA352144907SCN5Ac.2041C>A (p.His681Asn)
c.1912C>A (p.His638Asn)
3g.38597951G>ACA433333289SCN5Ac.2040C>T (p.Arg680=)
c.1911C>T (p.Arg637=)
3g.38597951G>CCA433333292SCN5Ac.2040C>G (p.Arg680=)
c.1911C>G (p.Arg637=)
3g.38597951G>TCA433333293SCN5Ac.2040C>A (p.Arg680=)
c.1911C>A (p.Arg637=)
3g.38597952C>ACA352144908SCN5Ac.2039G>T (p.Arg680Leu)
c.1910G>T (p.Arg637Leu)
gnomAD v4
3g.38597952C=CA1358584317SCN5Ac.2039G= (p.Arg680=)
c.1910G= (p.Arg637=)
3g.38597952C>GCA352144909SCN5Ac.2039G>C (p.Arg680Pro)
c.1910G>C (p.Arg637Pro)
3g.38597952C>TCA015757SCN5Ac.2039G>A (p.Arg680His)
c.1910G>A (p.Arg637His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38597953G>ACA059629SCN5Ac.2038C>T (p.Arg680Cys)
c.1909C>T (p.Arg637Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38597953G>CCA352144910SCN5Ac.2038C>G (p.Arg680Gly)
c.1909C>G (p.Arg637Gly)
3g.38597953G=CA1358584322SCN5Ac.2038C= (p.Arg680=)
c.1909C= (p.Arg637=)
3g.38597953G>TCA352144911SCN5Ac.2038C>A (p.Arg680Ser)
c.1909C>A (p.Arg637Ser)
gnomAD v4
3g.38597954A>CCA433333305SCN5Ac.2037T>G (p.Ser679=)
c.1908T>G (p.Ser636=)
gnomAD v4
3g.38597954A>GCA433333304SCN5Ac.2037T>C (p.Ser679=)
c.1908T>C (p.Ser636=)
3g.38597954A>TCA433333303SCN5Ac.2037T>A (p.Ser679=)
c.1908T>A (p.Ser636=)
3g.38597955G>ACA352144913SCN5Ac.2036C>T (p.Ser679Phe)
c.1907C>T (p.Ser636Phe)
3g.38597955G>CCA352144914SCN5Ac.2036C>G (p.Ser679Cys)
c.1907C>G (p.Ser636Cys)
gnomAD v4
3g.38597955G>TCA352144912SCN5Ac.2036C>A (p.Ser679Tyr)
c.1907C>A (p.Ser636Tyr)
3g.38597956A>CCA352144915SCN5Ac.2035T>G (p.Ser679Ala)
c.1906T>G (p.Ser636Ala)
3g.38597956A>GCA352144916SCN5Ac.2035T>C (p.Ser679Pro)
c.1906T>C (p.Ser636Pro)
3g.38597956A>TCA352144917SCN5Ac.2035T>A (p.Ser679Thr)
c.1906T>A (p.Ser636Thr)
3g.38597957C>ACA352144918SCN5Ac.2034G>T (p.Glu678Asp)
c.1905G>T (p.Glu635Asp)
3g.38597957C=CA1358584325SCN5Ac.2034G= (p.Glu678=)
c.1905G= (p.Glu635=)
3g.38597957C>GCA352144919SCN5Ac.2034G>C (p.Glu678Asp)
c.1905G>C (p.Glu635Asp)
3g.38597957C>TCA059616SCN5Ac.2034G>A (p.Glu678=)
c.1905G>A (p.Glu635=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38597958T>ACA352144920SCN5Ac.2033A>T (p.Glu678Val)
c.1904A>T (p.Glu635Val)
3g.38597958T>CCA352144922SCN5Ac.2033A>G (p.Glu678Gly)
c.1904A>G (p.Glu635Gly)
3g.38597958T>GCA352144921SCN5Ac.2033A>C (p.Glu678Ala)
c.1904A>C (p.Glu635Ala)
3g.38597959C>ACA352144923SCN5Ac.2032G>T (p.Glu678Ter)
c.1903G>T (p.Glu635Ter)
dbSNP
3g.38597959C=CA1358584329SCN5Ac.2032G= (p.Glu678=)
c.1903G= (p.Glu635=)
3g.38597959C>GCA352144924SCN5Ac.2032G>C (p.Glu678Gln)
c.1903G>C (p.Glu635Gln)
3g.38597959C>TCA352144925SCN5Ac.2032G>A (p.Glu678Lys)
c.1903G>A (p.Glu635Lys)
COSMIC COSMIC COSMIC
3g.38597960C>ACA352144926SCN5Ac.2031G>T (p.Glu677Asp)
c.1902G>T (p.Glu634Asp)
3g.38597960C=CA1358584330SCN5Ac.2031G= (p.Glu677=)
c.1902G= (p.Glu634=)
3g.38597960C>GCA352144927SCN5Ac.2031G>C (p.Glu677Asp)
c.1902G>C (p.Glu634Asp)
3g.38597960C>TCA72932631SCN5Ac.2031G>A (p.Glu677=)
c.1902G>A (p.Glu634=)
dbSNP
3g.38597964_38597969delCA2577553391SCN5Ac.2026_2031del
c.1897_1902del
3g.38597961T>ACA059609SCN5Ac.2030A>T (p.Glu677Val)
c.1901A>T (p.Glu634Val)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38597961T>CCA352144929SCN5Ac.2030A>G (p.Glu677Gly)
c.1901A>G (p.Glu634Gly)
dbSNP
3g.38597961T>GCA352144928SCN5Ac.2030A>C (p.Glu677Ala)
c.1901A>C (p.Glu634Ala)
3g.38597961T=CA1358584333SCN5Ac.2030A= (p.Glu677=)
c.1901A= (p.Glu634=)
3g.38597962C>ACA352144931SCN5Ac.2029G>T (p.Glu677Ter)
c.1900G>T (p.Glu634Ter)
dbSNP
3g.38597962C=CA1358584336SCN5Ac.2029G= (p.Glu677=)
c.1900G= (p.Glu634=)
3g.38597962C>GCA352144930SCN5Ac.2029G>C (p.Glu677Gln)
c.1900G>C (p.Glu634Gln)
3g.38597962C>TCA352144932SCN5Ac.2029G>A (p.Glu677Lys)
c.1900G>A (p.Glu634Lys)
gnomAD v4
3g.38597963T>ACA352144933SCN5Ac.2028A>T (p.Leu676Phe)
c.1899A>T (p.Leu633Phe)
3g.38597963T>CCA433333326SCN5Ac.2028A>G (p.Leu676=)
c.1899A>G (p.Leu633=)
3g.38597963T>GCA352144934SCN5Ac.2028A>C (p.Leu676Phe)
c.1899A>C (p.Leu633Phe)
3g.38597964A>CCA352144935SCN5Ac.2027T>G (p.Leu676Ter)
c.1898T>G (p.Leu633Ter)
3g.38597964A>GCA352144936SCN5Ac.2027T>C (p.Leu676Ser)
c.1898T>C (p.Leu633Ser)
ClinVar dbSNP gnomAD v4
3g.38597964A>TCA352144937SCN5Ac.2027T>A (p.Leu676Ter)
c.1898T>A (p.Leu633Ter)
3g.38597965A>CCA352144938SCN5Ac.2026T>G (p.Leu676Val)
c.1897T>G (p.Leu633Val)
3g.38597965A>GCA433333329SCN5Ac.2026T>C (p.Leu676=)
c.1897T>C (p.Leu633=)
3g.38597965A>TCA352144939SCN5Ac.2026T>A (p.Leu676Ile)
c.1897T>A (p.Leu633Ile)
3g.38597966C>ACA352144940SCN5Ac.2025G>T (p.Glu675Asp)
c.1896G>T (p.Glu632Asp)
COSMIC COSMIC COSMIC
3g.38597966C=CA1358584340SCN5Ac.2025G= (p.Glu675=)
c.1896G= (p.Glu632=)
3g.38597966C>GCA352144941SCN5Ac.2025G>C (p.Glu675Asp)
c.1896G>C (p.Glu632Asp)
3g.38597966C>TCA433333330SCN5Ac.2025G>A (p.Glu675=)
c.1896G>A (p.Glu632=)
dbSNP gnomAD v2 gnomAD v4
3g.38597968_38597969delCA2586971901SCN5Ac.2024_2025del
c.1895_1896del
3g.38597967T>ACA352144942SCN5Ac.2024A>T (p.Glu675Val)
c.1895A>T (p.Glu632Val)
3g.38597967T>CCA352144943SCN5Ac.2024A>G (p.Glu675Gly)
c.1895A>G (p.Glu632Gly)
3g.38597967T>GCA352144944SCN5Ac.2024A>C (p.Glu675Ala)
c.1895A>C (p.Glu632Ala)
3g.38597968C>ACA352144945SCN5Ac.2024-1G>T (n.2024-1G>T)
c.1895-1G>T (n.1895-1G>T)
3g.38597968C>GCA352144946SCN5Ac.2024-1G>C (n.2024-1G>C)
c.1895-1G>C (n.1895-1G>C)
3g.38597968C>TCA352144947SCN5Ac.2024-1G>A (n.2024-1G>A)
c.1895-1G>A (n.1895-1G>A)
ClinVar dbSNP
3g.38597969T>ACA352144950SCN5Ac.2024-2A>T (n.2024-2A>T)
c.1895-2A>T (n.1895-2A>T)
3g.38597969T>CCA352144948SCN5Ac.2024-2A>G (n.2024-2A>G)
c.1895-2A>G (n.1895-2A>G)
3g.38597969T>GCA352144949SCN5Ac.2024-2A>C (n.2024-2A>C)
c.1895-2A>C (n.1895-2A>C)
3g.38597970G=CA1358584342SCN5Ac.2024-3C= (n.2024-3C=)
c.1895-3C= (n.1895-3C=)
3g.38597970G>TCA1358584343SCN5Ac.2024-3C>A (n.2024-3C>A)
c.1895-3C>A (n.1895-3C>A)
dbSNP
3g.38597972G>ACA059598SCN5Ac.2024-5C>T (n.2024-5C>T)
c.1895-5C>T (n.1895-5C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38597972G=CA1358584345SCN5Ac.2024-5C= (n.2024-5C=)
c.1895-5C= (n.1895-5C=)
3g.38597973G>ACA059603SCN5Ac.2024-6C>T (n.2024-6C>T)
c.1895-6C>T (n.1895-6C>T)
dbSNP ExAC gnomAD v2
3g.38597973G>CCA2665114223SCN5Ac.2024-6C>G (n.2024-6C>G)
c.1895-6C>G (n.1895-6C>G)
gnomAD v4
3g.38597973G=CA1358584347SCN5Ac.2024-6C= (n.2024-6C=)
c.1895-6C= (n.1895-6C=)
3g.38597973G>TCA2840078080SCN5Ac.2024-6C>A (n.2024-6C>A)
c.1895-6C>A (n.1895-6C>A)
3g.38597974G>ACA2665114224SCN5Ac.2024-7C>T (n.2024-7C>T)
c.1895-7C>T (n.1895-7C>T)
gnomAD v4
3g.38597974G>TCA2840078081SCN5Ac.2024-7C>A (n.2024-7C>A)
c.1895-7C>A (n.1895-7C>A)
3g.38597975G>ACA542615622SCN5Ac.2024-8C>T (n.2024-8C>T)
c.1895-8C>T (n.1895-8C>T)
dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC
3g.38597975G=CA1358584349SCN5Ac.2024-8C= (n.2024-8C=)
c.1895-8C= (n.1895-8C=)
3g.38597978A=CA1358584353SCN5Ac.2024-11T= (n.2024-11T=)
c.1895-11T= (n.1895-11T=)
3g.38597978A>TCA72932638SCN5Ac.2024-11T>A (n.2024-11T>A)
c.1895-11T>A (n.1895-11T>A)
dbSNP gnomAD v4

Number of alleles fetched