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)
1093TP53P151H
PRO151HIS,P112H,P19H
NM_000546.5:c.452C>A,NP_000537.3:p.Pro151His,NC_000017.10:g.7578478G>T,ENST00000269305.4:c.452C>Amissense_variant
3765TP53P151S
3767TP53P152L
3794TP53P152T
3785TP53P177F
3786TP53P177H
3784TP53P177S
3778TP53P219H
3318TP53P250L
1049TP53P278S
RS17849781
ENST00000269305.4:c.832C>T,NM_000546.5:c.832C>T,NP_000537.3:p.Pro278Ser,NC_000017.10:g.7577106G>Amissense_variant
504TP53P47S
PRO47SER,RS1800371
NM_000546.5:c.139C>T,NP_000537.3:p.Pro47Ser,NC_000017.10:g.7579548G>A,ENST00000269305.4:c.139C>Tmissense_variant
531TP53P72R
PRO72ARG,P33R,RS1042522
NM_000546.5:c.215C>G,NP_000537.3:p.Pro72Arg,NC_000017.10:g.7579472G>C,ENST00000269305.4:c.215C>Gmissense_variant
3761TP53P98L
3760TP53P98S
3777TP53Q144P
4102TP53R156H
3795TP53R156P
4115TP53R158G
1695TP53R158H
ARG158HIS
ENST00000269305.4:c.473G>Amissense_variant
1699TP53R158L
ARG158LEU
ENST00000269305.4:c.473G>Tmissense_variant
116TP53R175H
ARG175HIS,RS28934578,R43H,R136H
NM_000546.5:c.524G>A,NP_000537.3:p.Arg175His,NC_000017.10:g.7578406C>T,ENST00000269305.4:c.524G>Amissense_variant
3796TP53R181C
3797TP53R181G
3798TP53R181H
3390TP53R181P
2711TP53R213*
R213X,ARG213TER,RS397516436,R81*
NM_000546.6:c.637C>T,ENST00000269305.9:c.637C>Tstop_gained
1109TP53R213P
ARG213PRO,R174P,R81P,RS587778720
NM_000546.5:c.638G>C,NP_000537.3:p.Arg213Pro,NC_000017.10:g.7578211C>G,ENST00000269305.4:c.638G>Cmissense_variant
117TP53R248Q
ARG248GLN,RS11540652
NM_000546.5:c.743G>A,NP_000537.3:p.Arg248Gln,NC_000017.10:g.7577538C>T,ENST00000269305.4:c.743G>Amissense_variant
118TP53R248W
ARG248TRP,RS121912651
NM_000546.5:c.742C>T,NP_000537.3:p.Arg248Trp,NC_000017.10:g.7577539G>A,ENST00000269305.4:c.742C>Tmissense_variant
119TP53R249
ARG249
NC_000017.10:g.7577535C>Gprotein_altering_variant
1696TP53R249Smissense_variant
121TP53R273C
ARG273CYS,RS121913343
NM_000546.5:c.817C>T,NP_000537.3:p.Arg273Cys,NC_000017.10:g.7577121G>A,ENST00000269305.4:c.817C>Tmissense_variant
122TP53R273H
ARG273HIS,RS28934576
NM_000546.5:c.818G>A,NP_000537.3:p.Arg273His,NC_000017.10:g.7577120C>T,ENST00000269305.4:c.818G>Amissense_variant
918TP53R273L
RS28934576,ARG273LEU
NM_000546.5:c.818G>T,NP_000537.3:p.Arg273Leu,NC_000017.10:g.7577120C>A,ENST00000269305.4:c.818G>Tmissense_variant
1697TP53R280K
R148K,R241K,ARG280LYS
ENST00000269305.4:c.839G>A,NC_000017.10:g.7577099C>T,NM_000546.5:c.839G>A,NP_000537.3:p.Arg280Lysmissense_variant
1698TP53R280T
R148T,R241T,ARG241THR
NM_000546.5:c.839G>C,NP_000537.3:p.Arg280Thr,NC_000017.10:g.7577099C>G,ENST00000269305.4:c.839G>Cmissense_variant
1108TP53R282L
ARG282LEU,R150L,R243L,RS730882008
NM_000546.5:c.845G>T,NP_000537.3:p.Arg282Leu,NC_000017.10:g.7577093C>A,ENST00000269305.4:c.845G>Tmissense_variant
916TP53R282W
RS28934574
NM_000546.5:c.844C>T,NP_000537.3:p.Arg282Trp,NC_000017.10:g.7577094G>A,ENST00000269305.4:c.844C>Tmissense_variant
3799TP53R283H
3582TP53R337P
3579TP53R342P
4968TP53R72P
2777TP53S241F
3788TP53S241T
3684TP53T125T
3782TP53T230S
223TP53Truncating Mutationframeshift_truncation
1092TP53V157F
RS121912654,VAL157PHE
NM_000546.5:c.469G>T,NP_000537.3:p.Val157Phe,NC_000017.10:g.7578461C>A,ENST00000269305.4:c.469G>Tmissense_variant
4123TP53V272G
3790TP53V274F