Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154903983G>ACA414905964F8c.5921C>T (p.Ser1974Phe)
c.5816C>T (p.Ser1939Phe)
COSMIC COSMIC
Xg.154903983G>CCA414905966F8c.5921C>G (p.Ser1974Cys)
c.5816C>G (p.Ser1939Cys)
Xg.154903983G>TCA414905968F8c.5921C>A (p.Ser1974Tyr)
c.5816C>A (p.Ser1939Tyr)
Xg.154903984A>CCA414905972F8c.5920T>G (p.Ser1974Ala)
c.5815T>G (p.Ser1939Ala)
Xg.154903984A>GCA414905974F8c.5920T>C (p.Ser1974Pro)
c.5815T>C (p.Ser1939Pro)
Xg.154903984A>TCA414905976F8c.5920T>A (p.Ser1974Thr)
c.5815T>A (p.Ser1939Thr)
Xg.154903985A>CCA414905979F8c.5919T>G (p.His1973Gln)
c.5814T>G (p.His1938Gln)
Xg.154903985A>GCA519356229F8c.5919T>C (p.His1973=)
c.5814T>C (p.His1938=)
Xg.154903985A>TCA414905981F8c.5919T>A (p.His1973Gln)
c.5814T>A (p.His1938Gln)
Xg.154903986T>ACA414905984F8c.5918A>T (p.His1973Leu)
c.5813A>T (p.His1938Leu)
ClinVar dbSNP gnomAD v4
Xg.154903986T>CCA414905988F8c.5918A>G (p.His1973Arg)
c.5813A>G (p.His1938Arg)
dbSNP
Xg.154903986T>GCA414905985F8c.5918A>C (p.His1973Pro)
c.5813A>C (p.His1938Pro)
Xg.154903986T=CA2466828160F8c.5918A= (p.His1973=)
c.5813A= (p.His1938=)
Xg.154903987G>ACA414905989F8c.5917C>T (p.His1973Tyr)
c.5812C>T (p.His1938Tyr)
Xg.154903987G>CCA414905990F8c.5917C>G (p.His1973Asp)
c.5812C>G (p.His1938Asp)
Xg.154903987G>TCA414905991F8c.5917C>A (p.His1973Asn)
c.5812C>A (p.His1938Asn)
Xg.154903988G>ACA519356233F8c.5916C>T (p.Ile1972=)
c.5811C>T (p.Ile1937=)
COSMIC COSMIC
Xg.154903988G>CCA414905993F8c.5916C>G (p.Ile1972Met)
c.5811C>G (p.Ile1937Met)
dbSNP
Xg.154903988G>TCA519356236F8c.5916C>A (p.Ile1972=)
c.5811C>A (p.Ile1937=)
Xg.154903988_154903990delinsGATCA2466828161F8c.5914_5916delinsATC (p.Ile1972=)
c.5809_5811delinsATC (p.Ile1937=)
Xg.154903989A=CA2466828162F8c.5915T= (p.Ile1972=)
c.5810T= (p.Ile1937=)
Xg.154903989A>CCA414905995F8c.5915T>G (p.Ile1972Ser)
c.5810T>G (p.Ile1937Ser)
Xg.154903989A>GCA414905996F8c.5915T>C (p.Ile1972Thr)
c.5810T>C (p.Ile1937Thr)
dbSNP
Xg.154903989A>TCA414905998F8c.5915T>A (p.Ile1972Asn)
c.5810T>A (p.Ile1937Asn)
Xg.154903989_154903990delCA873340712F8c.5914_5915del (p.Ile1972ProfsTer19)
c.5809_5810del (p.Ile1937ProfsTer19)
ClinVar dbSNP
Xg.154903990delCA2695237957F8c.5914del (p.Ile1972SerfsTer?)
c.5809del (p.Ile1937SerfsTer?)
Xg.154903990T>ACA414906012F8c.5914A>T (p.Ile1972Phe)
c.5809A>T (p.Ile1937Phe)
Xg.154903990T>CCA414906015F8c.5914A>G (p.Ile1972Val)
c.5809A>G (p.Ile1937Val)
Xg.154903990T>GCA414906017F8c.5914A>C (p.Ile1972Leu)
c.5809A>C (p.Ile1937Leu)
Xg.154903991G>ACA519356239F8c.5913C>T (p.Asn1971=)
c.5808C>T (p.Asn1936=)
Xg.154903991G>CCA414906027F8c.5913C>G (p.Asn1971Lys)
c.5808C>G (p.Asn1936Lys)
Xg.154903991G>TCA414906024F8c.5913C>A (p.Asn1971Lys)
c.5808C>A (p.Asn1936Lys)
Xg.154903992T>ACA414906029F8c.5912A>T (p.Asn1971Ile)
c.5807A>T (p.Asn1936Ile)
Xg.154903992T>CCA414906031F8c.5912A>G (p.Asn1971Ser)
c.5807A>G (p.Asn1936Ser)
Xg.154903992T>GCA414906034F8c.5912A>C (p.Asn1971Thr)
c.5807A>C (p.Asn1936Thr)
Xg.154903993T>ACA414906037F8c.5911A>T (p.Asn1971Tyr)
c.5806A>T (p.Asn1936Tyr)
Xg.154903993T>CCA414906038F8c.5911A>G (p.Asn1971Asp)
c.5806A>G (p.Asn1936Asp)
Xg.154903993T>GCA414906039F8c.5911A>C (p.Asn1971His)
c.5806A>C (p.Asn1936His)
dbSNP
Xg.154903993T=CA2466828163F8c.5911A= (p.Asn1971=)
c.5806A= (p.Asn1936=)
Xg.154903994T>ACA414906040F8c.5910A>T (p.Glu1970Asp)
c.5805A>T (p.Glu1935Asp)
Xg.154903994T>CCA519356243F8c.5910A>G (p.Glu1970=)
c.5805A>G (p.Glu1935=)
Xg.154903994T>GCA414906041F8c.5910A>C (p.Glu1970Asp)
c.5805A>C (p.Glu1935Asp)
Xg.154903995T>ACA414906043F8c.5909A>T (p.Glu1970Val)
c.5804A>T (p.Glu1935Val)
Xg.154903995T>CCA414906044F8c.5909A>G (p.Glu1970Gly)
c.5804A>G (p.Glu1935Gly)
Xg.154903995T>GCA414906047F8c.5909A>C (p.Glu1970Ala)
c.5804A>C (p.Glu1935Ala)
Xg.154903996C>ACA414906049F8c.5908G>T (p.Glu1970Ter)
c.5803G>T (p.Glu1935Ter)
Xg.154903996C>GCA414906050F8c.5908G>C (p.Glu1970Gln)
c.5803G>C (p.Glu1935Gln)
Xg.154903996C>TCA414906048F8c.5908G>A (p.Glu1970Lys)
c.5803G>A (p.Glu1935Lys)
Xg.154903997A>CCA414906054F8c.5907T>G (p.Asn1969Lys)
c.5802T>G (p.Asn1934Lys)
Xg.154903997A>GCA519356246F8c.5907T>C (p.Asn1969=)
c.5802T>C (p.Asn1934=)

Number of alleles fetched