Entrez Gene

Basic Information
Gene ID	11230
Name	PRAF2
Synonymous	PRA1 domain family, member 2;PRAF2;PRA1 domain family, member 2
Definition	Jena-Muenchen 4\|PRA1 family protein 2
Position	Xp11.23
Gene Type	protein-coding

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
COSMIC somatic mutation [Top]
c.351G>A; p.A117A; 23:49072479-49072479	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.428G>A; p.R143H; 23:49071978-49071978	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.32C>T; p.A11V; 23:49073956-49073956	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.283C>T; p.R95C; 23:49072547-49072547	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.397+9C>G; p.?; 23:49072424-49072424	oesophagus; lower_third	carcinoma; squamous_cell_carcinoma	Unknown
c.56C>T; p.S19L; 23:49073932-49073932	skin	malignant_melanoma	Substitution - Missense
c.168C>G; p.L56L; 23:49073820-49073820	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.459C>A; p.I153I; 23:49071947-49071947	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.427C>T; p.R143C; 23:49071979-49071979	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.23C>T; p.P8L; 23:49073965-49073965	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.59C>T; p.A20V; 23:49073929-49073929	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.175G>T; p.A59S; 23:49073813-49073813	lung	carcinoma; small_cell_carcinoma	Substitution - Missense
c.87C>A; p.D29E; 23:49073901-49073901	upper_aerodigestive_tract; pharynx	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.94C>T; p.R32*; 23:49073894-49073894	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Nonsense
c.3G>T; p.M1I; 23:49073985-49073985	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.350C>T; p.A117V; 23:49072480-49072480	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.426G>T; p.L142L; 23:49071980-49071980	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.183C>T; p.Y61Y; 23:49072647-49072647	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.408G>A; p.V136V; 23:49071998-49071998	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.313G>A; p.A105T; 23:49072517-49072517	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.494T>G; p.L165R; 23:49071912-49071912	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.110T>C; p.V37A; 23:49073878-49073878	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.146T>G; p.L49R; 23:49073842-49073842	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.287G>A; p.R96H; 23:49072543-49072543	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.227T>G; p.V76G; 23:49072603-49072603	eye; uveal_tract	malignant_melanoma	Substitution - Missense
c.156C>T; p.F52F; 23:49073832-49073832	breast	carcinoma	Substitution - coding silent
c.511G>C; p.G171R; 23:49071895-49071895	breast	other; fibroadenoma	Substitution - Missense
c.109G>A; p.V37I; 23:49073879-49073879	pancreas	carcinoma	Substitution - Missense

COSMIC somatic mutation [Top]