| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 2151 | ||
Name | F2RL2 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.16T>C; p.F6L; 5:76623215-76623215 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1012T>G; p.F338V; 5:76617695-76617695 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.729C>A; p.T243T; 5:76617978-76617978 |
stomach | adenocarcinoma | Substitution - coding silent |
c.967A>G; p.I323V; 5:76617740-76617740 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1111T>A; p.Y371N; 5:76617596-76617596 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1046T>G; p.L349R; 5:76617661-76617661 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.523G>A; p.G175S; 5:76618184-76618184 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.492C>T; p.V164V; 5:76618215-76618215 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.877G>A; p.D293N; 5:76617830-76617830 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.174C>T; p.G58G; 5:76618533-76618533 |
soft_tissue; blood_vessel | angiosarcoma | Substitution - coding silent |
c.1052G>C; p.S351T; 5:76617655-76617655 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.624C>A; p.T208T; 5:76618083-76618083 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.27T>C; p.A9A; 5:76623204-76623204 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.860G>A; p.R287Q; 5:76617847-76617847 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.72A>C; p.E24D; 5:76618635-76618635 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.122G>A; p.R41H; 5:76618585-76618585 |
haematopoietic_and_lymphoid_tissue; lymph_node | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.101_102CC>TT; p.T34I; 5:76618605-76618606 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.322G>A; p.G108S; 5:76618385-76618385 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.240G>A; p.V80V; 5:76618467-76618467 |
skin | malignant_melanoma | Substitution - coding silent |
c.326T>C; p.V109A; 5:76618381-76618381 |
central_nervous_system; brainstem | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1104C>T; p.S368S; 5:76617603-76617603 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.362T>G; p.F121C; 5:76618345-76618345 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.489G>C; p.E163D; 5:76618218-76618218 |
central_nervous_system; cerebellum | primitive_neuroectodermal_tumour-medulloblastoma; SHH_subtype | Substitution - Missense |
c.489G>C; p.E163D; 5:76618218-76618218 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma; medullomyoblastoma | Substitution - Missense |
c.459T>C; p.H153H; 5:76618248-76618248 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.140C>A; p.S47Y; 5:76618567-76618567 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.587T>C; p.V196A; 5:76618120-76618120 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.188C>T; p.T63M; 5:76618519-76618519 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.168G>A; p.L56L; 5:76618539-76618539 |
skin | malignant_melanoma | Substitution - coding silent |
c.421C>T; p.L141F; 5:76618286-76618286 |
skin | malignant_melanoma | Substitution - Missense |
c.337G>A; p.A113T; 5:76618370-76618370 |
prostate | carcinoma | Substitution - Missense |
c.977C>A; p.A326D; 5:76617730-76617730 |
soft_tissue; blood_vessel | angiosarcoma | Substitution - Missense |
c.686delT; p.F229fs*3; 5:76618021-76618021 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Deletion - Frameshift |
c.752C>G; p.T251S; 5:76617955-76617955 |
skin | malignant_melanoma | Substitution - Missense |
c.797T>C; p.L266S; 5:76617910-76617910 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.859C>A; p.R287R; 5:76617848-76617848 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.924G>T; p.V308V; 5:76617783-76617783 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.777A>T; p.Q259H; 5:76617930-76617930 |
skin; leg | malignant_melanoma; nodular | Substitution - Missense |
c.561C>G; p.I187M; 5:76618146-76618146 |
breast | carcinoma | Substitution - Missense |
c.133C>G; p.P45A; 5:76618574-76618574 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1112A>T; p.Y371F; 5:76617595-76617595 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.245A>T; p.N82I; 5:76618462-76618462 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.428G>T; p.C143F; 5:76618279-76618279 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.98C>A; p.P33Q; 5:76618609-76618609 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.148G>A; p.E50K; 5:76618559-76618559 |
skin | malignant_melanoma | Substitution - Missense |
c.148G>A; p.E50K; 5:76618559-76618559 |
breast | carcinoma | Substitution - Missense |
c.1061A>T; p.D354V; 5:76617646-76617646 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.16T>G; p.F6V; 5:76623215-76623215 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.876C>T; p.Y292Y; 5:76617831-76617831 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.360C>T; p.F120F; 5:76618347-76618347 |
skin | malignant_melanoma | Substitution - coding silent |
c.358T>A; p.F120I; 5:76618349-76618349 |
skin | malignant_melanoma | Substitution - Missense |
c.70G>A; p.E24K; 5:76618637-76618637 |
skin | malignant_melanoma | Substitution - Missense |
c.421>TT; p.L141fs*9; 5:76618286-76618286 |
skin | malignant_melanoma | Complex - frameshift |
c.871G>T; p.A291S; 5:76617836-76617836 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.503C>T; p.A168V; 5:76618204-76618204 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.134C>A; p.P45Q; 5:76618573-76618573 |
thyroid | carcinoma | Substitution - Missense |
c.293C>A; p.P98H; 5:76618414-76618414 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.293C>A; p.P98H; 5:76618414-76618414 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.293C>A; p.P98H; 5:76618414-76618414 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.474C>A; p.N158K; 5:76618233-76618233 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.933C>T; p.T311T; 5:76617774-76617774 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.933C>T; p.T311T; 5:76617774-76617774 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.513C>T; p.V171V; 5:76618194-76618194 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.842G>A; p.C281Y; 5:76617865-76617865 |
lung | carcinoma; large_cell_carcinoma | Substitution - Missense |
c.586G>A; p.V196I; 5:76618121-76618121 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.586G>A; p.V196I; 5:76618121-76618121 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; plasma_cell_myeloma | Substitution - Missense |
c.988T>A; p.Y330N; 5:76617719-76617719 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1076T>G; p.F359C; 5:76617631-76617631 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.806T>G; p.F269C; 5:76617901-76617901 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Substitution - Missense |
c.709C>A; p.L237I; 5:76617998-76617998 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.43T>C; p.L15L; 5:76623188-76623188 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.64+1G>A; p.?; 5:76623166-76623166 |
NS | malignant_melanoma | Unknown |
c.64+1G>A; p.?; 5:76623166-76623166 |
NS | malignant_melanoma | Unknown |
c.700G>A; p.E234K; 5:76618007-76618007 |
skin | malignant_melanoma | Substitution - Missense |
c.988T>C; p.Y330H; 5:76617719-76617719 |
kidney | other; neoplasm | Substitution - Missense |
c.1077T>A; p.F359L; 5:76617630-76617630 |
skin | malignant_melanoma | Substitution - Missense |
c.257G>A; p.G86E; 5:76618450-76618450 |
skin | malignant_melanoma | Substitution - Missense |
c.145G>A; p.E49K; 5:76618562-76618562 |
skin | malignant_melanoma | Substitution - Missense |
c.1074T>C; p.Y358Y; 5:76617633-76617633 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.1074T>C; p.Y358Y; 5:76617633-76617633 |
liver | carcinoma | Substitution - coding silent |
c.422T>C; p.L141P; 5:76618285-76618285 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.702A>T; p.E234D; 5:76618005-76618005 |
skin | malignant_melanoma | Substitution - Missense |
c.189delG; p.I64fs*3; 5:76618518-76618518 |
skin | malignant_melanoma | Deletion - Frameshift |
c.1050T>C; p.N350N; 5:76617657-76617657 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |