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 ID | Gene | Variant | HGVS | Type(s) |
|---|---|---|---|---|
| 4113 | TP53 | C124R | ||
| 924 | TP53 | C135W CYS135TRP,C3W,C96W | NM_000546.5:c.405C>G,NP_000537.3:p.Cys135Trp,NC_000017.10:g.7578525G>C,ENST00000269305.4:c.405C>G | missense_variant |
| 2648 | TP53 | C238Y CYS238TYR | NC_000017.10:g.7577568C>T,NM_000546.5:c.713G>A,NP_000537.3:p.Cys238Tyr,ENST00000269305.4:c.713G>A | missense_variant |
| 1062 | TP53 | C242F RS121912655 | NM_000546.5:c.725G>T,NP_000537.3:p.Cys242Phe,NC_000017.10:g.7577556C>A,ENST00000269305.4:c.725G>T | missense_variant |
| 1063 | TP53 | C242S RS121912655 | missense_variant | |
| 1064 | TP53 | C242Y RS121912655 | NM_000546.5:c.725G>A,NP_000537.3:p.Cys242Tyr,NC_000017.10:g.7577556C>T,ENST00000269305.4:c.725G>A | missense_variant |
| 1300 | TP53 | CONSERVED DOMAIN MUT | ||
| 3401 | TP53 | D259V | ||
| 1044 | TP53 | D281E ASP281GLU,D149E,D242E | NM_000546.5:c.843C>G,NP_000537.3:p.Asp281Glu,NC_000017.10:g.7577095G>C,ENST0000029305.4:c.843C>G | missense_variant |
| 3792 | TP53 | D281N | ||
| 242 | TP53 | DNA Binding Domain Mutation | DNA_binding_site | |
| 221 | TP53 | Deleterious Mutation | ||
| 3780 | TP53 | E224K | ||
| 3772 | TP53 | E258K | ||
| 1043 | TP53 | E285K GLU285LYS | ENST00000269305.4:c.853G>A | missense_variant |
| 915 | TP53 | E286K | missense_variant | |
| 4106 | TP53 | E68G | ||
| 1053 | TP53 | F270S PHE270SER,F138S,F231S | NC_000017.10:g.7577129A>G,NM_000546.5:c.809T>C,NP_000537.3:p.Phe270Ser,ENST00000269305.4:c.809T>C | missense_variant |
| 3419 | TP53 | G154S | ||
| 1060 | TP53 | G244S GLY244SER,G112S,G205S | NM_000546.5:c.730G>A,NP_000537.3:p.Gly244Ser,NC_000017.10:g.7577551C>T,ENST00000269305.4:c.730G>A | missense_variant |
| 1036 | TP53 | G245D RS121912656 | NC_000017.10:g.7577547C>T,NM_000546.5:c.734G>A,NP_000537.3:p.Gly245Asp,ENST00000269305.4:c.734G>A | missense_variant |
| 879 | TP53 | G245S RS28934575 | NC_000017.10:g.7577548C>T,NM_000546.5:c.733G>A,NP_000537.3:p.Gly245Ser,ENST00000269305.4:c.733G>A | missense_variant |
| 3773 | TP53 | G262D | ||
| 3774 | TP53 | G266E | ||
| 1055 | TP53 | G266R | missense_variant | |
| 4122 | TP53 | G266V | ||
| 3791 | TP53 | G279E | ||
| 4112 | TP53 | H115Y | ||
| 3783 | TP53 | H168Y | ||
| 4103 | TP53 | H178P | ||
| 1082 | TP53 | H179R HIS179ARG,H140R,H47R | NC_000017.10:g.7578394T>C,NM_000546.5:c.536A>G,NP_000537.3:p.His179Arg,ENST00000269305.4:c.536A>G | missense_variant |
| 1083 | TP53 | H179Y HIS179TYR,H140Y,H47Y | NC_000017.10:g.7578395G>A,NM_000546.5:c.535C>T,NP_000537.3:p.His179Tyr,ENST00000269305.4:c.535C>T | missense_variant |
| 1079 | TP53 | H193R | NC_000017.10:g.7578271T>C,NM_000546.5:c.578A>G,NP_000537.3:p.His193Arg,ENST00000269305.4:c.578A>G | missense_variant |
| 3768 | TP53 | I162F | ||
| 3764 | TP53 | K139E | ||
| 4111 | TP53 | L111R | ||
| 4114 | TP53 | L139N | ||
| 3771 | TP53 | L252F | ||
| 3801 | TP53 | L257P | ||
| 3775 | TP53 | L308M | ||
| 3776 | TP53 | L323P | ||
| 3580 | TP53 | L330P | ||
| 3581 | TP53 | L330R | ||
| 3583 | TP53 | L344P | ||
| 4452 | TP53 | Loss | ||
| 1066 | TP53 | M237I MET237ILE | ENST00000269305.4:c.711G>T | missense_variant |
| 3789 | TP53 | M246L | ||
| 222 | TP53 | Mutation | protein_altering_variant | |
| 3787 | TP53 | N239S | ||
| 1306 | TP53 | Overexpression |