| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 6045 |
Name | RNF2 |
Synonymous | ring finger protein 2;RNF2;ring finger protein 2 |
Definition | E3 ubiquitin-protein ligase RING2|HIP2-interacting protein 3|RING finger protein 1B|RING finger protein BAP-1|huntingtin-interacting protein 2-interacting protein 3|protein DinG |
Position | 1q25.3 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.305C>T; p.P102L; 1:185093117-185093117 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.587G>A; p.R196Q; 1:185098194-185098194 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.746A>C; p.K249T; 1:185099799-185099799 |
biliary_tract; gallbladder | carcinoma; adenocarcinoma | Substitution - Missense |
c.189T>C; p.T63T; 1:185091680-185091680 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.50G>A; p.W17*; 1:185087603-185087603 |
urinary_tract; bladder | carcinoma | Substitution - Nonsense |
c.591C>T; p.T197T; 1:185098198-185098198 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.472C>T; p.R158*; 1:185098079-185098079 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.242G>A; p.R81K; 1:185091733-185091733 |
skin; face | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.926T>G; p.F309C; 1:185100216-185100216 |
eye; uveal_tract | malignant_melanoma; spindle | Substitution - Missense |
c.11C>T; p.A4V; 1:185087564-185087564 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.797G>A; p.R266K; 1:185099850-185099850 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.82C>T; p.P28S; 1:185087635-185087635 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.248G>A; p.G83D; 1:185091739-185091739 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.344C>T; p.P115L; 1:185093156-185093156 |
skin | malignant_melanoma | Substitution - Missense |
c.136C>G; p.H46D; 1:185091627-185091627 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.821G>A; p.S274N; 1:185099874-185099874 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.224G>T; p.C75F; 1:185091715-185091715 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.375G>C; p.E125D; 1:185093187-185093187 |
breast | carcinoma | Substitution - Missense |
c.272G>A; p.R91Q; 1:185093084-185093084 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.817C>T; p.R273*; 1:185099870-185099870 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.872A>T; p.Y291F; 1:185099925-185099925 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.258A>C; p.E86D; 1:185093070-185093070 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.368A>C; p.H123P; 1:185093180-185093180 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.174G>C; p.L58F; 1:185091665-185091665 |
thyroid | carcinoma | Substitution - Missense |
c.157A>T; p.I53F; 1:185091648-185091648 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.133C>T; p.L45L; 1:185091624-185091624 |
breast | carcinoma | Substitution - coding silent |
c.210delT; p.C72fs*23; 1:185091701-185091701 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.320A>G; p.D107G; 1:185093132-185093132 |
breast | carcinoma; HER-positive_carcinoma | Substitution - Missense |
c.900C>T; p.G300G; 1:185099953-185099953 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.900C>T; p.G300G; 1:185099953-185099953 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.856G>A; p.A286T; 1:185099909-185099909 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.77G>A; p.R26Q; 1:185087630-185087630 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.77G>A; p.R26Q; 1:185087630-185087630 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.77G>A; p.R26Q; 1:185087630-185087630 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.77G>A; p.R26Q; 1:185087630-185087630 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.343C>T; p.P115S; 1:185093155-185093155 |
skin | malignant_melanoma | Substitution - Missense |
c.381A>G; p.V127V; 1:185093193-185093193 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.760G>A; p.A254T; 1:185099813-185099813 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.818G>A; p.R273Q; 1:185099871-185099871 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.818G>A; p.R273Q; 1:185099871-185099871 |
biliary_tract; bile_duct | carcinoma; adenocarcinoma | Substitution - Missense |
c.358T>C; p.Y120H; 1:185093170-185093170 |
skin | malignant_melanoma | Substitution - Missense |
c.293G>T; p.R98I; 1:185093105-185093105 |
breast | carcinoma | Substitution - Missense |
c.183C>T; p.T61T; 1:185091674-185091674 |
autonomic_ganglia | neuroblastoma | Substitution - coding silent |
c.350G>A; p.R117H; 1:185093162-185093162 |
pancreas | carcinoma | Substitution - Missense |
c.128G>A; p.R43Q; 1:185091619-185091619 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.128G>A; p.R43Q; 1:185091619-185091619 |
breast | carcinoma | Substitution - Missense |
c.100G>A; p.D34N; 1:185091591-185091591 |
skin; extremity | malignant_melanoma | Substitution - Missense |
c.34C>T; p.P12S; 1:185087587-185087587 |
skin | malignant_melanoma | Substitution - Missense |
c.339T>G; p.I113M; 1:185093151-185093151 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.924delT; p.S310fs*12; 1:185100214-185100214 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.473G>A; p.R158Q; 1:185098080-185098080 |
breast | carcinoma | Substitution - Missense |
c.759C>T; p.N253N; 1:185099812-185099812 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1A>G; p.M1V; 1:185087554-185087554 |
ovary | other; neoplasm | Substitution - Missense |
c.577A>T; p.S193C; 1:185098184-185098184 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.988G>A; p.A330T; 1:185100278-185100278 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |