| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 83596 |
Name | BCL2L12 |
Synonymous | BCL2-like 12 (proline rich);BCL2L12;BCL2-like 12 (proline rich) |
Definition | Bcl-2 related proline-rich protein|bcl-2-like protein 12 |
Position | 19q13.3 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.147G>A; p.V49V; 19:49665970-49665970 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.848C>G; p.A283G; 19:49670382-49670382 |
breast | carcinoma | Substitution - Missense |
c.58G>T; p.E20*; 19:49665881-49665881 |
breast | carcinoma | Substitution - Nonsense |
c.887C>T; p.T296I; 19:49670421-49670421 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.420C>T; p.C140C; 19:49667079-49667079 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.547G>C; p.E183Q; 19:49668895-49668895 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.801C>T; p.P267P; 19:49670335-49670335 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.738C>T; p.F246F; 19:49670272-49670272 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.895G>A; p.G299R; 19:49670429-49670429 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.29C>T; p.P10L; 19:49665852-49665852 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; hairy_cell_leukaemia | Substitution - Missense |
c.29C>T; p.P10L; 19:49665852-49665852 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; hairy_cell_leukaemia | Substitution - Missense |
c.727T>C; p.S243P; 19:49670261-49670261 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.108G>T; p.P36P; 19:49665931-49665931 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.863G>A; p.R288Q; 19:49670397-49670397 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.478C>T; p.R160C; 19:49667137-49667137 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.365C>A; p.P122H; 19:49667024-49667024 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.382A>G; p.T128A; 19:49667041-49667041 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.791G>A; p.R264Q; 19:49670325-49670325 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.439_440insC; p.S149fs*2; 19:49667098-49667099 |
large_intestine; rectum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.8G>A; p.R3Q; 19:49665831-49665831 |
liver | carcinoma | Substitution - Missense |
c.8G>A; p.R3Q; 19:49665831-49665831 |
liver | carcinoma | Substitution - Missense |
c.646C>G; p.L216V; 19:49669080-49669080 |
liver | carcinoma | Substitution - Missense |
c.646C>G; p.L216V; 19:49669080-49669080 |
liver | carcinoma | Substitution - Missense |
c.478C>T; p.R160C; 19:49667137-49667137 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.592T>G; p.L198V; 19:49669026-49669026 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.172A>T; p.I58L; 19:49665995-49665995 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.51C>T; p.F17F; 19:49665874-49665874 |
NS | malignant_melanoma | Substitution - coding silent |
c.51C>T; p.F17F; 19:49665874-49665874 |
NS | malignant_melanoma | Substitution - coding silent |
c.29C>T; p.P10L; 19:49665852-49665852 |
NS | malignant_melanoma | Substitution - Missense |
c.577C>T; p.P193S; 19:49668925-49668925 |
skin | malignant_melanoma | Substitution - Missense |
c.51_52CC>TT; p.R18W; 19:49665874-49665875 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.52C>T; p.R18W; 19:49665875-49665875 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.52C>T; p.R18W; 19:49665875-49665875 |
skin | malignant_melanoma | Substitution - Missense |
c.52C>T; p.R18W; 19:49665875-49665875 |
skin | malignant_melanoma | Substitution - Missense |
c.52C>T; p.R18W; 19:49665875-49665875 |
skin | malignant_melanoma | Substitution - Missense |
c.52C>T; p.R18W; 19:49665875-49665875 |
skin | malignant_melanoma | Substitution - Missense |
c.52C>T; p.R18W; 19:49665875-49665875 |
skin | malignant_melanoma | Substitution - Missense |
c.416_417CC>TT; p.P139L; 19:49667075-49667076 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.51C>T; p.F17F; 19:49665874-49665874 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.51C>T; p.F17F; 19:49665874-49665874 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.19C>T; p.L7L; 19:49665842-49665842 |
skin | malignant_melanoma | Substitution - coding silent |
c.955-3C>T; p.?; 19:49673695-49673695 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Unknown |
c.823G>A; p.E275K; 19:49670357-49670357 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.582C>T; p.P194P; 19:49668930-49668930 |
skin | malignant_melanoma | Substitution - coding silent |
c.738C>T; p.F246F; 19:49670272-49670272 |
skin | malignant_melanoma | Substitution - coding silent |
c.738C>T; p.F246F; 19:49670272-49670272 |
skin | malignant_melanoma | Substitution - coding silent |
c.514C>A; p.P172T; 19:49668862-49668862 |
skin | malignant_melanoma | Substitution - Missense |
c.578C>T; p.P193L; 19:49668926-49668926 |
skin | malignant_melanoma | Substitution - Missense |
c.499C>A; p.P167T; 19:49667158-49667158 |
skin | malignant_melanoma | Substitution - Missense |
c.30C>T; p.P10P; 19:49665853-49665853 |
skin | malignant_melanoma | Substitution - coding silent |
c.415C>T; p.P139S; 19:49667074-49667074 |
skin | malignant_melanoma | Substitution - Missense |
c.39T>G; p.P13P; 19:49665862-49665862 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.587C>T; p.P196L; 19:49668935-49668935 |
skin | malignant_melanoma | Substitution - Missense |
c.888C>T; p.T296T; 19:49670422-49670422 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.24C>T; p.F8F; 19:49665847-49665847 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.24C>T; p.F8F; 19:49665847-49665847 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.24C>T; p.F8F; 19:49665847-49665847 |
skin | malignant_melanoma | Substitution - coding silent |
c.24C>T; p.F8F; 19:49665847-49665847 |
skin | malignant_melanoma | Substitution - coding silent |
c.24C>T; p.F8F; 19:49665847-49665847 |
skin | malignant_melanoma | Substitution - coding silent |
c.24C>T; p.F8F; 19:49665847-49665847 |
skin | malignant_melanoma | Substitution - coding silent |
c.46G>A; p.G16S; 19:49665869-49665869 |
skin; scalp | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.122G>A; p.W41*; 19:49665945-49665945 |
skin | malignant_melanoma | Substitution - Nonsense |
c.690G>A; p.S230S; 19:49670224-49670224 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.519C>T; p.D173D; 19:49668867-49668867 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.467C>G; p.S156C; 19:49667126-49667126 |
thyroid | carcinoma | Substitution - Missense |
c.88G>A; p.E30K; 19:49665911-49665911 |
thyroid | carcinoma | Substitution - Missense |
c.233G>A; p.G78D; 19:49666056-49666056 |
thyroid | other; neoplasm | Substitution - Missense |
c.169C>G; p.L57V; 19:49665992-49665992 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.633G>A; p.R211R; 19:49669067-49669067 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.633G>A; p.R211R; 19:49669067-49669067 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |