| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 3184 |
Name | HNRNPD |
Synonymous | heterogeneous nuclear ribonucleoprotein D (AU-rich element RNA binding protein 1, 37kDa);HNRNPD;heterogeneous nuclear ribonucleoprotein D (AU-rich element RNA binding protein 1, 37kDa) |
Definition | ARE-binding protein AUFI, type A|heterogeneous nuclear ribonucleoprotein D0|hnRNP D0 |
Position | 4q21 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.443C>T; p.S148L; 4:82359487-82359487 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.936C>T; p.Y312Y; 4:82356601-82356601 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.990T>C; p.G330G; 4:82356547-82356547 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.540G>T; p.P180P; 4:82358740-82358740 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.724_725delAA; p.K242fs*8; 4:82357341-82357342 |
breast | carcinoma | Deletion - Frameshift |
c.380C>T; p.T127I; 4:82359550-82359550 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.370G>A; p.V124I; 4:82359560-82359560 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.756T>C; p.C252C; 4:82356893-82356893 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.551T>A; p.I184N; 4:82358729-82358729 |
haematopoietic_and_lymphoid_tissue; lymph_node | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.549A>C; p.K183N; 4:82358731-82358731 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.815G>A; p.R272K; 4:82356834-82356834 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.789_794delTCAGCA; p.Y263_Q265>*; 4:82356855-82356860 |
endometrium | carcinoma; endometrioid_carcinoma | Complex - deletion inframe |
c.51G>A; p.A17A; 4:82373628-82373628 |
ovary | other; neoplasm | Substitution - coding silent |
c.995A>G; p.Y332C; 4:82356542-82356542 |
breast | carcinoma | Substitution - Missense |
c.334G>A; p.D112N; 4:82359596-82359596 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.838C>T; p.R280C; 4:82356811-82356811 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.862C>G; p.Q288E; 4:82356675-82356675 |
breast | carcinoma; HER-positive_carcinoma | Substitution - Missense |
c.1052G>A; p.S351N; 4:82355350-82355350 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.734A>G; p.H245R; 4:82357332-82357332 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.933T>G; p.G311G; 4:82356604-82356604 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.260C>T; p.S87F; 4:82371558-82371558 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.985T>C; p.Y329H; 4:82356552-82356552 |
skin | malignant_melanoma | Substitution - Missense |
c.720G>T; p.M240I; 4:82357346-82357346 |
breast | carcinoma | Substitution - Missense |
c.555_556insT; p.V186fs*10; 4:82358724-82358725 |
large_intestine | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.214A>T; p.K72*; 4:82373465-82373465 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; Burkitt_lymphoma | Substitution - Nonsense |
c.721G>T; p.E241*; 4:82357345-82357345 |
breast | carcinoma | Substitution - Nonsense |
c.625G>T; p.E209*; 4:82357441-82357441 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.625G>A; p.E209K; 4:82357441-82357441 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.726G>T; p.K242N; 4:82357340-82357340 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.223G>A; p.E75K; 4:82373456-82373456 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.619G>T; p.E207*; 4:82358661-82358661 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.528A>C; p.K176N; 4:82358752-82358752 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1032G>T; p.R344S; 4:82355370-82355370 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.711G>T; p.K237N; 4:82357355-82357355 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.406C>T; p.R136*; 4:82359524-82359524 |
urinary_tract; bladder | carcinoma | Substitution - Nonsense |
c.839G>A; p.R280H; 4:82356810-82356810 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.328A>G; p.K110E; 4:82359602-82359602 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.550delA; p.I184fs*15; 4:82358730-82358730 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.550delA; p.I184fs*15; 4:82358730-82358730 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.737_738insCA; p.V247fs*9; 4:82357328-82357329 |
stomach | carcinoma; intestinal_adenocarcinoma | Insertion - Frameshift |
c.565C>A; p.L189I; 4:82358715-82358715 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.445G>T; p.E149*; 4:82359485-82359485 |
prostate | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.772A>G; p.M258V; 4:82356877-82356877 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.714G>A; p.K238K; 4:82357352-82357352 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |