| Gene ID | 6236 |
| Symbol | RRAD |
| Synonymous | RAD|RAD1|REM3 |
| Full name | Ras-related associated with diabetes |
| Gene description | GTP-binding protein RAD|RAS (RAD and GEM) like GTP binding 3|ras associated with diabetes |
| Cytoband | 16q22 |
| Gene type | protein-coding |
| Synonymous | MIM:179503; HGNC:HGNC:10446; Ensembl:ENSG00000166592; HPRD:01536; Vega:OTTHUMG00000137511 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.644T>C; p.V215A; 16:66923521-66923521 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.836A>G; p.K279R; 16:66922167-66922167 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.429C>T; p.Y143Y; 16:66923861-66923861 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.382G>A; p.D128N; 16:66923908-66923908 |
skin | malignant_melanoma | Substitution - Missense |
c.509C>T; p.S170L; 16:66923656-66923656 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.454C>T; p.R152C; 16:66923711-66923711 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.403G>C; p.G135R; 16:66923887-66923887 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.267G>C; p.E89D; 16:66924913-66924913 |
breast | carcinoma | Substitution - Missense |
c.664G>A; p.A222T; 16:66922339-66922339 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.775G>A; p.E259K; 16:66922228-66922228 |
skin | malignant_melanoma | Substitution - Missense |
c.806G>A; p.R269Q; 16:66922197-66922197 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.788G>A; p.R263Q; 16:66922215-66922215 |
skin | malignant_melanoma | Substitution - Missense |
c.420C>T; p.L140L; 16:66923870-66923870 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.850C>T; p.R284C; 16:66922153-66922153 |
skin; extremity | malignant_melanoma | Substitution - Missense |
c.626G>A; p.R209H; 16:66923539-66923539 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.896C>T; p.S299F; 16:66922107-66922107 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.745C>T; p.R249C; 16:66922258-66922258 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.761G>A; p.R254H; 16:66922242-66922242 |
prostate | carcinoma | Substitution - Missense |
c.26G>T; p.G9V; 16:66925154-66925154 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.833C>A; p.A278E; 16:66922170-66922170 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.833C>A; p.A278E; 16:66922170-66922170 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.833C>A; p.A278E; 16:66922170-66922170 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.833C>A; p.A278E; 16:66922170-66922170 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.833C>A; p.A278E; 16:66922170-66922170 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.833C>A; p.A278E; 16:66922170-66922170 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.459G>A; p.W153*; 16:66923706-66923706 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Substitution - Nonsense |
c.389C>G; p.S130C; 16:66923901-66923901 |
liver | carcinoma | Substitution - Missense |
c.380A>G; p.Y127C; 16:66923910-66923910 |
breast | carcinoma | Substitution - Missense |
c.394G>C; p.V132L; 16:66923896-66923896 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.389C>G; p.S130C; 16:66923901-66923901 |
liver | carcinoma | Substitution - Missense |
c.889G>A; p.A297T; 16:66922114-66922114 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.886C>T; p.R296C; 16:66922117-66922117 |
skin | malignant_melanoma | Substitution - Missense |
c.886C>T; p.R296C; 16:66922117-66922117 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.886C>T; p.R296C; 16:66922117-66922117 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.886C>T; p.R296C; 16:66922117-66922117 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.807G>A; p.R269R; 16:66922196-66922196 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.385C>T; p.R129C; 16:66923905-66923905 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.363G>A; p.E121E; 16:66924817-66924817 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.833C>T; p.A278V; 16:66922170-66922170 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.833C>T; p.A278V; 16:66922170-66922170 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.597C>T; p.I199I; 16:66923568-66923568 |
skin | malignant_melanoma | Substitution - coding silent |
c.343G>C; p.E115Q; 16:66924837-66924837 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.843C>A; p.F281L; 16:66922160-66922160 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.663C>T; p.C221C; 16:66922340-66922340 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.664G>T; p.A222S; 16:66922339-66922339 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.812G>A; p.R271Q; 16:66922191-66922191 |
skin | malignant_melanoma | Substitution - Missense |
c.791G>A; p.R264Q; 16:66922212-66922212 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.791G>A; p.R264Q; 16:66922212-66922212 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.729_730GT>AC; p.L243>?; 16:66922273-66922274 |
large_intestine; colon | carcinoma; adenocarcinoma | Complex |
c.566G>A; p.R189H; 16:66923599-66923599 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.872G>A; p.R291H; 16:66922131-66922131 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.639C>T; p.V213V; 16:66923526-66923526 |
skin | malignant_melanoma | Substitution - coding silent |
c.839G>A; p.R280H; 16:66922164-66922164 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.783C>T; p.N261N; 16:66922220-66922220 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.563G>A; p.R188Q; 16:66923602-66923602 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.236C>T; p.S79L; 16:66924944-66924944 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.576_579delAACA; p.T193fs*93; 16:66923586-66923589 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.411G>T; p.E137D; 16:66923879-66923879 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |