Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38550360dupCA2319532SCN5Ac.6014dup (p.Ser2006PhefsTer7)
c.6017dup (p.Ser2007PhefsTer7)
c.5963dup (p.Ser1989PhefsTer7)
c.5855dup (p.Ser1953PhefsTer7)
c.5918dup (p.Ser1974PhefsTer7)
c.5888dup (p.Ser1964PhefsTer7)
c.5960dup (p.Ser1988PhefsTer7)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38550360delCA542269469SCN5Ac.6014del (p.Pro2005LeufsTer?)
c.6017del (p.Pro2006LeufsTer?)
c.5963del (p.Pro1988LeufsTer?)
c.5855del (p.Pro1952LeufsTer?)
c.5918del (p.Pro1973LeufsTer?)
c.5888del (p.Pro1963LeufsTer?)
c.5960del (p.Pro1987LeufsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38550358_38550360delCA542269470SCN5Ac.6012_6014del (p.Pro2005del)
c.6015_6017del (p.Pro2006del)
c.5961_5963del (p.Pro1988del)
c.5853_5855del (p.Pro1952del)
c.5916_5918del (p.Pro1973del)
c.5886_5888del (p.Pro1963del)
c.5958_5960del (p.Pro1987del)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38550355_38550364delCA1047007129SCN5Ac.6005_6014del (p.Asp2002ValfsTer?)
c.6008_6017del (p.Asp2003ValfsTer?)
c.5954_5963del (p.Asp1985ValfsTer?)
c.5846_5855del (p.Asp1949ValfsTer?)
c.5909_5918del (p.Asp1970ValfsTer?)
c.5879_5888del (p.Asp1960ValfsTer?)
c.5951_5960del (p.Asp1984ValfsTer?)
gnomAD v3 gnomAD v4
3g.38550359G>ACA065192SCN5Ac.6010C>T (p.Pro2004Ser)
c.6013C>T (p.Pro2005Ser)
c.5959C>T (p.Pro1987Ser)
c.5851C>T (p.Pro1951Ser)
c.5914C>T (p.Pro1972Ser)
c.5884C>T (p.Pro1962Ser)
c.5956C>T (p.Pro1986Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38550359G>CCA019590SCN5Ac.6010C>G (p.Pro2004Ala)
c.6013C>G (p.Pro2005Ala)
c.5959C>G (p.Pro1987Ala)
c.5851C>G (p.Pro1951Ala)
c.5914C>G (p.Pro1972Ala)
c.5884C>G (p.Pro1962Ala)
c.5956C>G (p.Pro1986Ala)
ClinVar dbSNP
3g.38550359G=CA1358561719SCN5Ac.6010C= (p.Pro2004=)
c.6013C= (p.Pro2005=)
c.5959C= (p.Pro1987=)
c.5851C= (p.Pro1951=)
c.5914C= (p.Pro1972=)
c.5884C= (p.Pro1962=)
c.5956C= (p.Pro1986=)
3g.38550359G>TCA352139093SCN5Ac.6010C>A (p.Pro2004Thr)
c.6013C>A (p.Pro2005Thr)
c.5959C>A (p.Pro1987Thr)
c.5851C>A (p.Pro1951Thr)
c.5914C>A (p.Pro1972Thr)
c.5884C>A (p.Pro1962Thr)
c.5956C>A (p.Pro1986Thr)
3g.38550360G>ACA433134159SCN5Ac.6009C>T (p.Phe2003=)
c.6012C>T (p.Phe2004=)
c.5958C>T (p.Phe1986=)
c.5850C>T (p.Phe1950=)
c.5913C>T (p.Phe1971=)
c.5883C>T (p.Phe1961=)
c.5955C>T (p.Phe1985=)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38550360G>CCA065185SCN5Ac.6009C>G (p.Phe2003Leu)
c.6012C>G (p.Phe2004Leu)
c.5958C>G (p.Phe1986Leu)
c.5850C>G (p.Phe1950Leu)
c.5913C>G (p.Phe1971Leu)
c.5883C>G (p.Phe1961Leu)
c.5955C>G (p.Phe1985Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38550360G=CA1358561720SCN5Ac.6009C= (p.Phe2003=)
c.6012C= (p.Phe2004=)
c.5958C= (p.Phe1986=)
c.5850C= (p.Phe1950=)
c.5913C= (p.Phe1971=)
c.5883C= (p.Phe1961=)
c.5955C= (p.Phe1985=)
3g.38550360G>TCA352139097SCN5Ac.6009C>A (p.Phe2003Leu)
c.6012C>A (p.Phe2004Leu)
c.5958C>A (p.Phe1986Leu)
c.5850C>A (p.Phe1950Leu)
c.5913C>A (p.Phe1971Leu)
c.5883C>A (p.Phe1961Leu)
c.5955C>A (p.Phe1985Leu)
3g.38550361_38550363dupCA2586965711SCN5Ac.6007_6009dup (p.Phe2003_Pro2004insPhe)
c.6010_6012dup (p.Phe2004_Pro2005insPhe)
c.5956_5958dup (p.Phe1986_Pro1987insPhe)
c.5848_5850dup (p.Phe1950_Pro1951insPhe)
c.5911_5913dup (p.Phe1971_Pro1972insPhe)
c.5881_5883dup (p.Phe1961_Pro1962insPhe)
c.5953_5955dup (p.Phe1985_Pro1986insPhe)
3g.38550361A=CA1358561721SCN5Ac.6008T= (p.Phe2003=)
c.6011T= (p.Phe2004=)
c.5957T= (p.Phe1986=)
c.5849T= (p.Phe1950=)
c.5912T= (p.Phe1971=)
c.5882T= (p.Phe1961=)
c.5954T= (p.Phe1985=)
3g.38550361A>CCA352139099SCN5Ac.6008T>G (p.Phe2003Cys)
c.6011T>G (p.Phe2004Cys)
c.5957T>G (p.Phe1986Cys)
c.5849T>G (p.Phe1950Cys)
c.5912T>G (p.Phe1971Cys)
c.5882T>G (p.Phe1961Cys)
c.5954T>G (p.Phe1985Cys)
ClinVar
3g.38550361A>GCA019586SCN5Ac.6008T>C (p.Phe2003Ser)
c.6011T>C (p.Phe2004Ser)
c.5957T>C (p.Phe1986Ser)
c.5849T>C (p.Phe1950Ser)
c.5912T>C (p.Phe1971Ser)
c.5882T>C (p.Phe1961Ser)
c.5954T>C (p.Phe1985Ser)
ClinVar dbSNP gnomAD v4
3g.38550361A>TCA352139102SCN5Ac.6008T>A (p.Phe2003Tyr)
c.6011T>A (p.Phe2004Tyr)
c.5957T>A (p.Phe1986Tyr)
c.5849T>A (p.Phe1950Tyr)
c.5912T>A (p.Phe1971Tyr)
c.5882T>A (p.Phe1961Tyr)
c.5954T>A (p.Phe1985Tyr)
3g.38550362A=CA1358561722SCN5Ac.6007T= (p.Phe2003=)
c.6010T= (p.Phe2004=)
c.5956T= (p.Phe1986=)
c.5848T= (p.Phe1950=)
c.5911T= (p.Phe1971=)
c.5881T= (p.Phe1961=)
c.5953T= (p.Phe1985=)
3g.38550362A>CCA019582SCN5Ac.6007T>G (p.Phe2003Val)
c.6010T>G (p.Phe2004Val)
c.5956T>G (p.Phe1986Val)
c.5848T>G (p.Phe1950Val)
c.5911T>G (p.Phe1971Val)
c.5881T>G (p.Phe1961Val)
c.5953T>G (p.Phe1985Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38550362A>GCA019578SCN5Ac.6007T>C (p.Phe2003Leu)
c.6010T>C (p.Phe2004Leu)
c.5956T>C (p.Phe1986Leu)
c.5848T>C (p.Phe1950Leu)
c.5911T>C (p.Phe1971Leu)
c.5881T>C (p.Phe1961Leu)
c.5953T>C (p.Phe1985Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38550362A>TCA065172SCN5Ac.6007T>A (p.Phe2003Ile)
c.6010T>A (p.Phe2004Ile)
c.5956T>A (p.Phe1986Ile)
c.5848T>A (p.Phe1950Ile)
c.5911T>A (p.Phe1971Ile)
c.5881T>A (p.Phe1961Ile)
c.5953T>A (p.Phe1985Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38550363G>ACA433134162SCN5Ac.6006C>T (p.Asp2002=)
c.6009C>T (p.Asp2003=)
c.5955C>T (p.Asp1985=)
c.5847C>T (p.Asp1949=)
c.5910C>T (p.Asp1970=)
c.5880C>T (p.Asp1960=)
c.5952C>T (p.Asp1984=)
dbSNP gnomAD v4
3g.38550363G>CCA352139106SCN5Ac.6006C>G (p.Asp2002Glu)
c.6009C>G (p.Asp2003Glu)
c.5955C>G (p.Asp1985Glu)
c.5847C>G (p.Asp1949Glu)
c.5910C>G (p.Asp1970Glu)
c.5880C>G (p.Asp1960Glu)
c.5952C>G (p.Asp1984Glu)
3g.38550363G=CA1358561723SCN5Ac.6006C= (p.Asp2002=)
c.6009C= (p.Asp2003=)
c.5955C= (p.Asp1985=)
c.5847C= (p.Asp1949=)
c.5910C= (p.Asp1970=)
c.5880C= (p.Asp1960=)
c.5952C= (p.Asp1984=)
3g.38550363G>TCA352139107SCN5Ac.6006C>A (p.Asp2002Glu)
c.6009C>A (p.Asp2003Glu)
c.5955C>A (p.Asp1985Glu)
c.5847C>A (p.Asp1949Glu)
c.5910C>A (p.Asp1970Glu)
c.5880C>A (p.Asp1960Glu)
c.5952C>A (p.Asp1984Glu)
3g.38550364T>ACA352139110SCN5Ac.6005A>T (p.Asp2002Val)
c.6008A>T (p.Asp2003Val)
c.5954A>T (p.Asp1985Val)
c.5846A>T (p.Asp1949Val)
c.5909A>T (p.Asp1970Val)
c.5879A>T (p.Asp1960Val)
c.5951A>T (p.Asp1984Val)
3g.38550364T>CCA352139111SCN5Ac.6005A>G (p.Asp2002Gly)
c.6008A>G (p.Asp2003Gly)
c.5954A>G (p.Asp1985Gly)
c.5846A>G (p.Asp1949Gly)
c.5909A>G (p.Asp1970Gly)
c.5879A>G (p.Asp1960Gly)
c.5951A>G (p.Asp1984Gly)
3g.38550364T>GCA352139113SCN5Ac.6005A>C (p.Asp2002Ala)
c.6008A>C (p.Asp2003Ala)
c.5954A>C (p.Asp1985Ala)
c.5846A>C (p.Asp1949Ala)
c.5909A>C (p.Asp1970Ala)
c.5879A>C (p.Asp1960Ala)
c.5951A>C (p.Asp1984Ala)
3g.38550365C>ACA352139115SCN5Ac.6004G>T (p.Asp2002Tyr)
c.6007G>T (p.Asp2003Tyr)
c.5953G>T (p.Asp1985Tyr)
c.5845G>T (p.Asp1949Tyr)
c.5908G>T (p.Asp1970Tyr)
c.5878G>T (p.Asp1960Tyr)
c.5950G>T (p.Asp1984Tyr)
gnomAD v4
3g.38550365C=CA1358561724SCN5Ac.6004G= (p.Asp2002=)
c.6007G= (p.Asp2003=)
c.5953G= (p.Asp1985=)
c.5845G= (p.Asp1949=)
c.5908G= (p.Asp1970=)
c.5878G= (p.Asp1960=)
c.5950G= (p.Asp1984=)
3g.38550365C>GCA352139117SCN5Ac.6004G>C (p.Asp2002His)
c.6007G>C (p.Asp2003His)
c.5953G>C (p.Asp1985His)
c.5845G>C (p.Asp1949His)
c.5908G>C (p.Asp1970His)
c.5878G>C (p.Asp1960His)
c.5950G>C (p.Asp1984His)
gnomAD v4
3g.38550365C>TCA065167SCN5Ac.6004G>A (p.Asp2002Asn)
c.6007G>A (p.Asp2003Asn)
c.5953G>A (p.Asp1985Asn)
c.5845G>A (p.Asp1949Asn)
c.5908G>A (p.Asp1970Asn)
c.5878G>A (p.Asp1960Asn)
c.5950G>A (p.Asp1984Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38550366G>ACA065162SCN5Ac.6003C>T (p.Ala2001=)
c.6006C>T (p.Ala2002=)
c.5952C>T (p.Ala1984=)
c.5844C>T (p.Ala1948=)
c.5907C>T (p.Ala1969=)
c.5877C>T (p.Ala1959=)
c.5949C>T (p.Ala1983=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38550366G>CCA433134166SCN5Ac.6003C>G (p.Ala2001=)
c.6006C>G (p.Ala2002=)
c.5952C>G (p.Ala1984=)
c.5844C>G (p.Ala1948=)
c.5907C>G (p.Ala1969=)
c.5877C>G (p.Ala1959=)
c.5949C>G (p.Ala1983=)
3g.38550366G=CA1358561725SCN5Ac.6003C= (p.Ala2001=)
c.6006C= (p.Ala2002=)
c.5952C= (p.Ala1984=)
c.5844C= (p.Ala1948=)
c.5907C= (p.Ala1969=)
c.5877C= (p.Ala1959=)
c.5949C= (p.Ala1983=)
3g.38550366G>TCA433134167SCN5Ac.6003C>A (p.Ala2001=)
c.6006C>A (p.Ala2002=)
c.5952C>A (p.Ala1984=)
c.5844C>A (p.Ala1948=)
c.5907C>A (p.Ala1969=)
c.5877C>A (p.Ala1959=)
c.5949C>A (p.Ala1983=)
ClinVar COSMIC COSMIC COSMIC
3g.38550366_38550367delCA1047007147SCN5Ac.6002_6003del (p.Ala2001GlyfsTer11)
c.6005_6006del (p.Ala2002GlyfsTer11)
c.5951_5952del (p.Ala1984GlyfsTer11)
c.5843_5844del (p.Ala1948GlyfsTer11)
c.5906_5907del (p.Ala1969GlyfsTer11)
c.5876_5877del (p.Ala1959GlyfsTer11)
c.5948_5949del (p.Ala1983GlyfsTer11)
gnomAD v3 gnomAD v4
3g.38550367G>ACA352139121SCN5Ac.6002C>T (p.Ala2001Val)
c.6005C>T (p.Ala2002Val)
c.5951C>T (p.Ala1984Val)
c.5843C>T (p.Ala1948Val)
c.5906C>T (p.Ala1969Val)
c.5876C>T (p.Ala1959Val)
c.5948C>T (p.Ala1983Val)
gnomAD v4 COSMIC COSMIC COSMIC
3g.38550367G>CCA352139122SCN5Ac.6002C>G (p.Ala2001Gly)
c.6005C>G (p.Ala2002Gly)
c.5951C>G (p.Ala1984Gly)
c.5843C>G (p.Ala1948Gly)
c.5906C>G (p.Ala1969Gly)
c.5876C>G (p.Ala1959Gly)
c.5948C>G (p.Ala1983Gly)
3g.38550367G>TCA352139124SCN5Ac.6002C>A (p.Ala2001Asp)
c.6005C>A (p.Ala2002Asp)
c.5951C>A (p.Ala1984Asp)
c.5843C>A (p.Ala1948Asp)
c.5906C>A (p.Ala1969Asp)
c.5876C>A (p.Ala1959Asp)
c.5948C>A (p.Ala1983Asp)
3g.38550368C>ACA065157SCN5Ac.6001G>T (p.Ala2001Ser)
c.6004G>T (p.Ala2002Ser)
c.5950G>T (p.Ala1984Ser)
c.5842G>T (p.Ala1948Ser)
c.5905G>T (p.Ala1969Ser)
c.5875G>T (p.Ala1959Ser)
c.5947G>T (p.Ala1983Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38550368C=CA1358561726SCN5Ac.6001G= (p.Ala2001=)
c.6004G= (p.Ala2002=)
c.5950G= (p.Ala1984=)
c.5842G= (p.Ala1948=)
c.5905G= (p.Ala1969=)
c.5875G= (p.Ala1959=)
c.5947G= (p.Ala1983=)
3g.38550368C>GCA352139125SCN5Ac.6001G>C (p.Ala2001Pro)
c.6004G>C (p.Ala2002Pro)
c.5950G>C (p.Ala1984Pro)
c.5842G>C (p.Ala1948Pro)
c.5905G>C (p.Ala1969Pro)
c.5875G>C (p.Ala1959Pro)
c.5947G>C (p.Ala1983Pro)
3g.38550368C>TCA10576613SCN5Ac.6001G>A (p.Ala2001Thr)
c.6004G>A (p.Ala2002Thr)
c.5950G>A (p.Ala1984Thr)
c.5842G>A (p.Ala1948Thr)
c.5905G>A (p.Ala1969Thr)
c.5875G>A (p.Ala1959Thr)
c.5947G>A (p.Ala1983Thr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38550369G>ACA019574SCN5Ac.6000C>T (p.Leu2000=)
c.6003C>T (p.Leu2001=)
c.5949C>T (p.Leu1983=)
c.5841C>T (p.Leu1947=)
c.5904C>T (p.Leu1968=)
c.5874C>T (p.Leu1958=)
c.5946C>T (p.Leu1982=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38550369G>CCA433134173SCN5Ac.6000C>G (p.Leu2000=)
c.6003C>G (p.Leu2001=)
c.5949C>G (p.Leu1983=)
c.5841C>G (p.Leu1947=)
c.5904C>G (p.Leu1968=)
c.5874C>G (p.Leu1958=)
c.5946C>G (p.Leu1982=)
3g.38550369G=CA1358561727SCN5Ac.6000C= (p.Leu2000=)
c.6003C= (p.Leu2001=)
c.5949C= (p.Leu1983=)
c.5841C= (p.Leu1947=)
c.5904C= (p.Leu1968=)
c.5874C= (p.Leu1958=)
c.5946C= (p.Leu1982=)
3g.38550369G>TCA433134172SCN5Ac.6000C>A (p.Leu2000=)
c.6003C>A (p.Leu2001=)
c.5949C>A (p.Leu1983=)
c.5841C>A (p.Leu1947=)
c.5904C>A (p.Leu1968=)
c.5874C>A (p.Leu1958=)
c.5946C>A (p.Leu1982=)
3g.38550370A>CCA352139129SCN5Ac.5999T>G (p.Leu2000Arg)
c.6002T>G (p.Leu2001Arg)
c.5948T>G (p.Leu1983Arg)
c.5840T>G (p.Leu1947Arg)
c.5903T>G (p.Leu1968Arg)
c.5873T>G (p.Leu1958Arg)
c.5945T>G (p.Leu1982Arg)
3g.38550370A>GCA352139127SCN5Ac.5999T>C (p.Leu2000Pro)
c.6002T>C (p.Leu2001Pro)
c.5948T>C (p.Leu1983Pro)
c.5840T>C (p.Leu1947Pro)
c.5903T>C (p.Leu1968Pro)
c.5873T>C (p.Leu1958Pro)
c.5945T>C (p.Leu1982Pro)
gnomAD v4

Number of alleles fetched