| Gene ID | 3626 |
| Symbol | INHBC |
| Synonymous | IHBC |
| Full name | inhibin, beta C |
| Gene description | activin beta-C chain|inhibin beta C chain |
| Cytoband | 12q13.1 |
| Gene type | protein-coding |
| Synonymous | MIM:601233; HGNC:HGNC:6068; HPRD:03136 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.814G>A; p.A272T; 12:57449777-57449777 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.814G>A; p.A272T; 12:57449777-57449777 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.745C>T; p.R249*; 12:57449708-57449708 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.299G>A; p.S100N; 12:57435185-57435185 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.843A>G; p.P281P; 12:57449806-57449806 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.466G>T; p.G156C; 12:57449429-57449429 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.277G>A; p.E93K; 12:57435163-57435163 |
skin | malignant_melanoma | Substitution - Missense |
c.950_951GT>AG; p.C317*; 12:57449913-57449914 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.879C>T; p.S293S; 12:57449842-57449842 |
skin | malignant_melanoma | Substitution - coding silent |
c.733A>G; p.R245G; 12:57449696-57449696 |
thyroid | carcinoma | Substitution - Missense |
c.811T>C; p.Y271H; 12:57449774-57449774 |
liver | carcinoma | Substitution - Missense |
c.498T>C; p.T166T; 12:57449461-57449461 |
breast | carcinoma; ductal_carcinoma | Substitution - coding silent |
c.498T>C; p.T166T; 12:57449461-57449461 |
breast | carcinoma; ductal_carcinoma | Substitution - coding silent |
c.405G>A; p.M135I; 12:57449368-57449368 |
ovary | other; neoplasm | Substitution - Missense |
c.204C>T; p.S68S; 12:57435090-57435090 |
skin | malignant_melanoma | Substitution - coding silent |
c.795C>T; p.I265I; 12:57449758-57449758 |
skin | malignant_melanoma | Substitution - coding silent |
c.408C>A; p.F136L; 12:57449371-57449371 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.986A>G; p.Y329C; 12:57449949-57449949 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.838T>C; p.C280R; 12:57449801-57449801 |
oesophagus | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.986A>G; p.Y329C; 12:57449949-57449949 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.927C>A; p.G309G; 12:57449890-57449890 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; essential_thrombocythaemia | Substitution - coding silent |
c.829A>T; p.I277L; 12:57449792-57449792 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.855A>C; p.A285A; 12:57449818-57449818 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.337C>A; p.R113S; 12:57449300-57449300 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.105A>G; p.E35E; 12:57434991-57434991 |
skin | malignant_melanoma | Substitution - coding silent |
c.421C>T; p.P141S; 12:57449384-57449384 |
skin | malignant_melanoma | Substitution - Missense |
c.792G>A; p.W264*; 12:57449755-57449755 |
skin | malignant_melanoma | Substitution - Nonsense |
c.588C>A; p.T196T; 12:57449551-57449551 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.40C>T; p.P14S; 12:57434926-57434926 |
skin | malignant_melanoma | Substitution - Missense |
c.959C>T; p.T320M; 12:57449922-57449922 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.959C>T; p.T320M; 12:57449922-57449922 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.959C>T; p.T320M; 12:57449922-57449922 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.959C>T; p.T320M; 12:57449922-57449922 |
stomach | adenocarcinoma | Substitution - Missense |
c.875C>A; p.A292D; 12:57449838-57449838 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.574C>T; p.Q192*; 12:57449537-57449537 |
breast | carcinoma | Substitution - Nonsense |
c.813C>T; p.Y271Y; 12:57449776-57449776 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.813C>T; p.Y271Y; 12:57449776-57449776 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.813C>T; p.Y271Y; 12:57449776-57449776 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.815C>T; p.A272V; 12:57449778-57449778 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.832G>T; p.G278W; 12:57449795-57449795 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.734G>A; p.R245K; 12:57449697-57449697 |
skin | malignant_melanoma | Substitution - Missense |
c.862C>T; p.P288S; 12:57449825-57449825 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.69C>T; p.G23G; 12:57434955-57434955 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.835C>T; p.Q279*; 12:57449798-57449798 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.488C>T; p.T163I; 12:57449451-57449451 |
skin | malignant_melanoma | Substitution - Missense |
c.705A>T; p.R235R; 12:57449668-57449668 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.431_432CC>GA; p.T144R; 12:57449394-57449395 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.510G>A; p.L170L; 12:57449473-57449473 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.961G>A; p.A321T; 12:57449924-57449924 |
skin | malignant_melanoma | Substitution - Missense |
c.787G>A; p.D263N; 12:57449750-57449750 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.521C>T; p.A174V; 12:57449484-57449484 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.564T>C; p.A188A; 12:57449527-57449527 |
stomach | adenocarcinoma | Substitution - coding silent |
c.1014G>T; p.K338N; 12:57449977-57449977 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.608G>A; p.G203D; 12:57449571-57449571 |
skin | malignant_melanoma | Substitution - Missense |
c.642A>T; p.G214G; 12:57449605-57449605 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - coding silent |
c.81A>C; p.P27P; 12:57434967-57434967 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.1005C>G; p.N335K; 12:57449968-57449968 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.715G>A; p.D239N; 12:57449678-57449678 |
skin | malignant_melanoma | Substitution - Missense |
c.616G>A; p.A206T; 12:57449579-57449579 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.24C>T; p.A8A; 12:57434910-57434910 |
skin | malignant_melanoma | Substitution - coding silent |
c.24C>T; p.A8A; 12:57434910-57434910 |
skin | malignant_melanoma | Substitution - coding silent |
c.216G>C; p.L72F; 12:57435102-57435102 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.157G>A; p.D53N; 12:57435043-57435043 |
skin | malignant_melanoma | Substitution - Missense |
c.948C>A; p.C316*; 12:57449911-57449911 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.819G>A; p.M273I; 12:57449782-57449782 |
skin | malignant_melanoma | Substitution - Missense |
c.746G>A; p.R249Q; 12:57449709-57449709 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.486C>T; p.L162L; 12:57449449-57449449 |
skin | malignant_melanoma | Substitution - coding silent |
c.769C>T; p.R257C; 12:57449732-57449732 |
skin | malignant_melanoma | Substitution - Missense |
c.965G>A; p.R322Q; 12:57449928-57449928 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.965G>A; p.R322Q; 12:57449928-57449928 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.965G>A; p.R322Q; 12:57449928-57449928 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |