| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 152559 | ||
Name | PAQR3 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.765T>G; p.I255M; 4:78923885-78923885 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.117C>T; p.S39S; 4:78939108-78939108 |
skin | malignant_melanoma | Substitution - coding silent |
c.327T>C; p.S109S; 4:78935142-78935142 |
skin | malignant_melanoma | Substitution - coding silent |
c.24C>T; p.S8S; 4:78939201-78939201 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.248T>G; p.F83C; 4:78935221-78935221 |
prostate | adenoma | Substitution - Missense |
c.487G>A; p.A163T; 4:78930187-78930187 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.897A>G; p.R299R; 4:78920578-78920578 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.326C>A; p.S109Y; 4:78935143-78935143 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.884T>C; p.V295A; 4:78920591-78920591 |
large_intestine | adenoma | Substitution - Missense |
c.525G>A; p.L175L; 4:78926698-78926698 |
skin | malignant_melanoma | Substitution - coding silent |
c.37G>C; p.E13Q; 4:78939188-78939188 |
upper_aerodigestive_tract; pharynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.573T>A; p.H191Q; 4:78926650-78926650 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.10A>G; p.K4E; 4:78939215-78939215 |
breast | carcinoma | Substitution - Missense |
c.726G>A; p.V242V; 4:78923924-78923924 |
breast | carcinoma | Substitution - coding silent |
c.672C>T; p.L224L; 4:78926551-78926551 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.60G>A; p.W20*; 4:78939165-78939165 |
ovary | carcinoma; serous_carcinoma | Substitution - Nonsense |
c.684T>A; p.I228I; 4:78926539-78926539 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.394C>T; p.R132W; 4:78930280-78930280 |
liver | carcinoma | Substitution - Missense |
c.394C>T; p.R132W; 4:78930280-78930280 |
liver | carcinoma | Substitution - Missense |
c.546C>T; p.I182I; 4:78926677-78926677 |
skin | malignant_melanoma | Substitution - coding silent |
c.385T>A; p.S129T; 4:78930289-78930289 |
skin | malignant_melanoma | Substitution - Missense |
c.563C>T; p.A188V; 4:78926660-78926660 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.563C>T; p.A188V; 4:78926660-78926660 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.268G>C; p.D90H; 4:78935201-78935201 |
breast | carcinoma | Substitution - Missense |
c.503A>G; p.N168S; 4:78930171-78930171 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.234_235GG>AA; p.G79S; 4:78935234-78935235 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.741T>A; p.A247A; 4:78923909-78923909 |
pancreas | carcinoma | Substitution - coding silent |
c.369G>T; p.V123V; 4:78930305-78930305 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.250T>C; p.F84L; 4:78935219-78935219 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.250T>C; p.F84L; 4:78935219-78935219 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.7C>G; p.Q3E; 4:78939218-78939218 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.775C>A; p.P259T; 4:78923875-78923875 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.300G>A; p.A100A; 4:78935169-78935169 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.278C>T; p.S93F; 4:78935191-78935191 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.278C>T; p.S93F; 4:78935191-78935191 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.768C>G; p.S256S; 4:78923882-78923882 |
skin | malignant_melanoma | Substitution - coding silent |
c.571C>A; p.H191N; 4:78926652-78926652 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.406_407insA; p.T136fs*32; 4:78930267-78930268 |
large_intestine; rectum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.59G>A; p.W20*; 4:78939166-78939166 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.587C>T; p.T196M; 4:78926636-78926636 |
breast | carcinoma | Substitution - Missense |
c.907C>T; p.P303S; 4:78920568-78920568 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.22A>C; p.S8R; 4:78939203-78939203 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.560T>G; p.F187C; 4:78926663-78926663 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.282G>A; p.V94V; 4:78935187-78935187 |
liver | carcinoma | Substitution - coding silent |
c.282G>A; p.V94V; 4:78935187-78935187 |
liver | carcinoma | Substitution - coding silent |
c.926C>T; p.S309L; 4:78920549-78920549 |
skin | malignant_melanoma | Substitution - Missense |
c.842C>T; p.A281V; 4:78920633-78920633 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.528C>T; p.I176I; 4:78926695-78926695 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.258G>T; p.L86L; 4:78935211-78935211 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - coding silent |
c.407_408insA; p.C137fs*31; 4:78930266-78930267 |
stomach | carcinoma; intestinal_adenocarcinoma | Insertion - Frameshift |
c.299C>T; p.A100V; 4:78935170-78935170 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.927A>G; p.S309S; 4:78920548-78920548 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.365C>T; p.S122F; 4:78930309-78930309 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.298G>T; p.A100S; 4:78935171-78935171 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.679G>C; p.G227R; 4:78926544-78926544 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.727A>G; p.M243V; 4:78923923-78923923 |
parathyroid | adenoma | Substitution - Missense |
c.133T>C; p.Y45H; 4:78939092-78939092 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; hairy_cell_leukaemia | Substitution - Missense |
c.244C>G; p.L82V; 4:78935225-78935225 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma; medullomyoblastoma | Substitution - Missense |
c.244C>G; p.L82V; 4:78935225-78935225 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.339C>T; p.F113F; 4:78935130-78935130 |
thyroid | other; neoplasm | Substitution - coding silent |
c.405_406insA; p.T136fs*32; 4:78930268-78930269 |
oesophagus | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.405_406insA; p.T136fs*32; 4:78930268-78930269 |
oesophagus | carcinoma; adenocarcinoma | Insertion - Frameshift |