CIViC Compass
Research use only — not FDA-cleared, not medical advice. Always consult FDA-approved labeling and a qualified clinician.

CIViC Variants

1951 variants indexed

Variant Types

Sequence Ontology (SO) terms describing the molecular consequence of each variant, as curated in CIViC. Hover a bar for the definition.

CIViC IDGeneVariantHGVSType(s)
5223PIK3CAE542V
882PIK3CAE545A
RS121913274,GLU545ALA
NM_006218.3:c.1634A>C,NP_006209.2:p.Glu545Ala,NC_000003.11:g.178936092A>C,ENST00000263967.3:c.1634A>Cmissense_variant
934PIK3CAE545D
RS121913275,GLU545ASP
NM_006218.3:c.1635G>C,NP_006209.2:p.Glu545Asp,NC_000003.11:g.178936093G>C,ENST00000263967.3:c.1635G>Cmissense_variant
883PIK3CAE545G
RS121913274,GLU545GLY
NM_006218.3:c.1634A>G,NP_006209.2:p.Glu545Gly,NC_000003.11:g.178936092A>G,ENST00000263967.3:c.1634A>Gmissense_variant
104PIK3CAE545K
GLU545LYS,RS104886003
NM_006218.3:c.1633G>A,NP_006209.2:p.Glu545Lys,ENST00000263967.3:c.1633G>A,NC_000003.11:g.178936091G>Amissense_variant
5256PIK3CAE545L
881PIK3CAE545Q
RS104886003,GLU545GLN
NM_006218.3:c.1633G>C,NP_006209.2:p.Glu545Gln,NC_000003.11:g.178936091G>C,ENST00000263967.3:c.1633G>Cmissense_variant
5257PIK3CAE545R
884PIK3CAE545V
RS121913274,GLU545VAL
NM_006218.3:c.1634A>T,NP_006209.2:p.Glu545Val,NC_000003.11:g.178936092A>T,ENST00000263967.3:c.1634A>Tmissense_variant
1500PIK3CAE81K
GLU81LYS,RS1057519929
NM_006218.3:c.241G>A,NP_006209.2:p.Glu81Lys,NC_000003.11:g.178916854G>A,ENST00000263967.3:c.241G>Amissense_variant
106PIK3CAExon 10 Mutation
EXON 9 MUTATION
exon_variant
105PIK3CAExon 21 Mutation
EXON 20 MUTATION
exon_variant
3667PIK3CAF930S
3437PIK3CAG1007R
1501PIK3CAG1049A
GLY1049ALA
ENST00000263967.3:c.3146G>C,NC_000003.11:g.178952091G>C,NM_006218.2:c.3146G>C,NP_006209.2:p.Gly1049Alamissense_variant
5231PIK3CAG1049C
5232PIK3CAG1049D
940PIK3CAG1049R
RS121913277,GLY1049ARG
NM_006218.3:c.3145G>C,NP_006209.2:p.Gly1049Arg,NC_000003.11:g.178952090G>C,ENST00000263967.3:c.3145G>Cmissense_variant
939PIK3CAG1049S
RS121913277,GLY1049SER
NM_006218.3:c.3145G>A,NP_006209.2:p.Gly1049Ser,NC_000003.11:g.178952090G>A,ENST00000263967.3:c.3145G>Amissense_variant
5228PIK3CAG106A
5229PIK3CAG106D
1201PIK3CAG106Rmissense_variant
5227PIK3CAG106S
1179PIK3CAG106Vmissense_variant
5230PIK3CAG118D
5213PIK3CAH1047D
5214PIK3CAH1047I
1151PIK3CAH1047L
RS121913279,HIS1047LEU
NM_006218.3:c.3140A>T,NP_006209.2:p.His1047Leu,NC_000003.11:g.178952085A>T,ENST00000263967.3:c.3140A>Tmissense_variant
5215PIK3CAH1047N
5216PIK3CAH1047P
5217PIK3CAH1047Q
107PIK3CAH1047R
HIS1047ARG,RS121913279
NM_006218.3:c.3140A>G,NP_006209.2:p.His1047Arg,ENST00000263967.3:c.3140A>G,NC_000003.11:g.178952085A>Gmissense_variant
5218PIK3CAH1047T
938PIK3CAH1047Y
RS121913281,HIS1047TYR
NM_006218.3:c.3139C>T,NP_006209.2:p.His1047Tyr,NC_000003.11:g.178952084C>T,ENST00000263967.3:c.3139C>Tmissense_variant
1235PIK3CAI391M
ILE391MET,RS2230461
NM_006218.3:c.1173A>G,NP_006209.2:p.Ile391Met,NC_000003.11:g.178927410A>G,ENST00000263967.3:c.1173A>Gmissense_variant
1202PIK3CAK111Emissense_variant
1234PIK3CAK111N
LYS111ASN,RS1057519934
NM_006218.3:c.333G>C,NP_006209.2:p.Lys111Asn,NC_000003.11:g.178916946G>C,ENST00000263967.3:c.333G>Cmissense_variant
5224PIK3CAK111R
3666PIK3CAK944N
3669PIK3CAK966E
3670PIK3CAL938*
937PIK3CAM1043I
RS121913283,MET1043ILE
NM_006218.3:c.3129G>T,NP_006209.2:p.Met1043Ile,NC_000003.11:g.178952074G>T,ENST00000263967.3:c.3129G>Tmissense_variant
5239PIK3CAM1043T
936PIK3CAM1043Vmissense_variant
311PIK3CAMutationgain_of_function_variant,transcript_variant
3438PIK3CAN1044K
5233PIK3CAN345D
5234PIK3CAN345H
5235PIK3CAN345I
930PIK3CAN345K
RS121913284,ASN345LYS
NM_006218.3:c.1035T>A,NP_006209.2:p.Asn345Lys,NC_000003.11:g.178921553T>A,ENST00000263967.3:c.1035T>Amissense_variant