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) |
|---|---|---|---|---|
| 5308 | EGFR | H773_V774insTH | ||
| 5303 | EGFR | H773delinsNPY | ||
| 5304 | EGFR | H773delinsPNPY | ||
| 5305 | EGFR | H773delinsYNPY | ||
| 5306 | EGFR | H773delinsYPNPY | ||
| 455 | EGFR | K467T LYS467THR | ENST00000275493.2:c.1400A>C,NC_000007.13:g.55227933A>C,NM_005228.3:c.1400A>C,NP_005219.2:p.Lys467Thr | missense_variant |
| 4409 | EGFR | K754E | ||
| 723 | EGFR | K757R LYS757ARG,RS397517102 | ENST00000275493.2:c.2270A>G,NC_000007.13:g.55242500A>G,NM_005228.3:c.2270A>G,NP_005219.2:p.Lys757Arg,NM_005228.5:c.2270A>G,NC_000007.14:g.55174807A>G | missense_variant |
| 1895 | EGFR | K806E LYS806GLU,RS754652044 | ENST00000275493.2:c.2416A>G,NM_001346898.1:c.2416A>G,NP_001333827.1:p.Lys806Glu,NC_000007.13:g.55249118A>G | missense_variant |
| 1891 | EGFR | L747P LEU747PRO | NM_005228.4:c.2239_2240delTTinsCC,NP_005219.2:p.Leu747Pro,NC_000007.13:g.55242469_55242470delTTinsCC,ENST00000275493.2:c.2239_2240delTTinsCC | missense_variant |
| 1012 | EGFR | L747_P753delinsS RS121913438 | inframe_deletion | |
| 1580 | EGFR | L747_S752delinsQ DEL L747-S752INSQ,LEU747_SER752DELINSGLN | NC_000007.14:g.55174776_55174793delinsCAA,NC_000007.13:g.55242469_55242486delinsCAA,ENST00000275493.7:c.2239_2256delinsCAA,ENSP00000275493.2:p.Leu747_Ser752delinsGln,NM_005228.5:c.2239_2256delinsCAA,NP_005219.2:p.Leu747_Ser752delinsGln | inframe_insertion,inframe_deletion,delins |
| 1457 | EGFR | L838P LEU838PRO | NC_000007.14:g.55191762T>C,NC_000007.13:g.55259455T>C,ENST00000275493.7:c.2513T>C,ENSP00000275493.2:p.Leu838Pro,NM_005228.5:c.2513T>C,NP_005219.2:p.Leu838Pro | missense_variant |
| 1018 | EGFR | L838V LEU838VAL | NM_005228.4:c.2512C>G,NP_005219.2:p.Leu838Val,NC_000007.13:g.55259454C>G,ENST00000275493.2:c.2512C>G | missense_variant |
| 33 | EGFR | L858R LEU858ARG,RS121434568,L813R,LEU813ARG | NC_000007.13:g.55259515T>G,NM_005228.4:c.2573T>G,ENST00000275493.2:c.2573T>G,NP_005219.2:p.Leu858Arg | missense_variant |
| 1866 | EGFR | L861 | ||
| 1020 | EGFR | L861Q RS121913444 | NM_005228.4:c.2582T>A,NP_005219.2:p.Leu861Gln,NC_000007.13:g.55259524T>A,ENST00000275493.2:c.2582T>A | missense_variant |
| 1477 | EGFR | L861R RS121913444,LEU861ARG | NM_005228.4:c.2582T>G,NP_005219.2:p.Leu861Arg,NC_000007.13:g.55259524T>G,NC_000007.14:g.55191831T>G,ENST00000275493.7:c.2582T>G,ENSP00000275493.2:p.Leu861Arg | missense_variant |
| 1664 | EGFR | M766_A767insAI | inframe_insertion | |
| 2213 | EGFR | M766_A767insASV | ||
| 442 | EGFR | Mutation | inframe_variant | |
| 5294 | EGFR | N771_P772insDN | ||
| 3304 | EGFR | N771_P772insL | ||
| 5295 | EGFR | N771_P772insRH | ||
| 5278 | EGFR | N771_P772insT | ||
| 5296 | EGFR | N771_P772insVDN | ||
| 5290 | EGFR | N771delinsCH | ||
| 5291 | EGFR | N771delinsGF | ||
| 1581 | EGFR | N771delinsGY N771>GY,ASN771DELINSGLYTYR | inframe_insertion,inframe_deletion,delins | |
| 5292 | EGFR | N771delinsRD | ||
| 5293 | EGFR | N771delinsSQRGH | ||
| 5276 | EGFR | N771dup | ||
| 1188 | EGFR | N826S N773S,N781S | ENST00000275493.2:c.2477A>G | missense_variant |
| 1896 | EGFR | N826Y ASN826TYR | ENST00000275493.2:c.2476A>T,NC_000007.13:g.55259418A>T,NC_000007.14:g.55191725A>T,NM_005228.3:c.2476A>T,NP_005219.2:p.Asn826Tyr | missense_variant |
| 1899 | EGFR | N842S ASN842SER | ENST00000275493.2:c.2525A>G | missense_variant |
| 193 | EGFR | Overexpression | ||
| 460 | EGFR | P753S PRO753SER,RS121913231 | NC_000007.13:g.55242487C>T,ENST00000275493.2:c.2257C>T,NM_005228.4:c.2257C>T,NP_005219.2:p.Pro753Ser | missense_variant |
| 5299 | EGFR | P772_H773insDNP | ||
| 5300 | EGFR | P772_H773insPHP | ||
| 5301 | EGFR | P772_H773insQ | ||
| 5302 | EGFR | P772_H773insRNP | ||
| 1667 | EGFR | P772_H773insYNP | inframe_insertion | |
| 1668 | EGFR | P772_V774insPHV | inframe_insertion | |
| 5297 | EGFR | P772delinsHR | ||
| 994 | EGFR | R108K ARG108LYS | NM_005228.4:c.323G>A,NP_005219.2:p.Arg108Lys,NC_000007.13:g.55211080G>A,ENST00000275493.2:c.323G>A | missense_variant |
| 3344 | EGFR | R222C ARG222CYS | missense_variant | |
| 3961 | EGFR | R252C | ||
| 454 | EGFR | R451C ARG451CYS,RS377567759 | NC_000007.13:g.55227884C>T,ENST00000275493.2:c.1351C>T,NM_001346898.1:c.1351C>T,NP_001333827.1:p.Arg451Cys | missense_variant |
| 2333 | EGFR | R705K ARG705LYS | ENST00000275493.2:c.2114G>A,NC_000007.13:g.55241666G>A,NM_005228.3:c.2114G>A,NP_005219.2:p.Arg705Lys | missense_variant |
| 1181 | EGFR | R776C R723C,R731C | ENST00000275493.2:c.2326C>T | missense_variant |