| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 57817 |
Name | HAMP |
Synonymous | hepcidin antimicrobial peptide;HAMP;hepcidin antimicrobial peptide |
Definition | hepcidin|liver-expressed antimicrobial peptide 1|putative liver tumor regressor |
Position | 19q13.1 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.93_94GG>AA; p.G32R; 19:35284791-35284792 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.97C>A; p.Q33K; 19:35284795-35284795 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.252G>A; p.T84T; 19:35285039-35285039 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.162G>C; p.Q54H; 19:35284949-35284949 |
breast | carcinoma | Substitution - Missense |
c.220C>T; p.H74Y; 19:35285007-35285007 |
skin | malignant_melanoma | Substitution - Missense |
c.175C>T; p.R59*; 19:35284962-35284962 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.147G>A; p.W49*; 19:35284845-35284845 |
skin | malignant_melanoma | Substitution - Nonsense |
c.166C>T; p.R56*; 19:35284953-35284953 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.238A>G; p.M80V; 19:35285025-35285025 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.90+4A>G; p.?; 19:35282671-35282671 |
biliary_tract; gallbladder | carcinoma; adenocarcinoma | Unknown |
c.206G>T; p.C69F; 19:35284993-35284993 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.18G>T; p.Q6H; 19:35282595-35282595 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.213C>T; p.G71G; 19:35285000-35285000 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.12C>A; p.S4R; 19:35282589-35282589 |
liver | carcinoma | Substitution - Missense |
c.12C>A; p.S4R; 19:35282589-35282589 |
liver | carcinoma | Substitution - Missense |
c.236G>T; p.G79V; 19:35285023-35285023 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.236G>T; p.G79V; 19:35285023-35285023 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.146G>A; p.W49*; 19:35284844-35284844 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.39_40insCTC; p.L18_A19insL; 19:35282616-35282617 |
endometrium | carcinoma; endometrioid_carcinoma | Insertion - In frame |
c.14C>T; p.S5F; 19:35282591-35282591 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.167G>A; p.R56Q; 19:35284954-35284954 |
skin | malignant_melanoma | Substitution - Missense |
c.150+1G>A; p.?; 19:35284849-35284849 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Unknown |
c.40_42delCTC; p.L18delL; 19:35282617-35282619 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - In frame |
c.211G>T; p.G71C; 19:35284998-35284998 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.40_42delCTC; p.L18delL; 19:35282617-35282619 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - In frame |
c.40_42delCTC; p.L18delL; 19:35282617-35282619 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - In frame |
c.182C>A; p.T61N; 19:35284969-35284969 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.151-1G>T; p.?; 19:35284937-35284937 |
lung | carcinoma; adenocarcinoma | Unknown |
c.63G>A; p.L21L; 19:35282640-35282640 |
skin | malignant_melanoma | Substitution - coding silent |