Cancer metastasis database

Annotation category 5

Gene information

Gene ID 8000
Symbol

PSCA

Synonymous

PRO232

Full name

prostate stem cell antigen

Gene description

-

Cytoband

8q24.2

Gene type

protein-coding

Synonymous

MIM:602470; HGNC:HGNC:9500; Ensembl:ENSG00000167653; HPRD:03919; Vega:OTTHUMG00000162077

COSMIC somatic mutation

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.92A>G; p.N31S; 8:142681393-142681393

skinmalignant_melanomaSubstitution - Missense

c.92A>G; p.N31S; 8:142681393-142681393

skinmalignant_melanomaSubstitution - Missense

c.191A>G; p.D64G; 8:142681978-142681978

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.78C>A; p.C26*; 8:142681379-142681379

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Nonsense

c.127C>T; p.R43C; 8:142681428-142681428

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.133C>T; p.R45C; 8:142681434-142681434

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.279G>T; p.P93P; 8:142682066-142682066

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.231C>A; p.C77*; 8:142682018-142682018

stomachcarcinoma; adenocarcinomaSubstitution - Nonsense

c.231C>A; p.C77*; 8:142682018-142682018

urinary_tract; bladdercarcinomaSubstitution - Nonsense

c.313G>A; p.G105S; 8:142682100-142682100

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; myelofibrosisSubstitution - Missense

c.126G>A; p.A42A; 8:142681427-142681427

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.208G>A; p.V70M; 8:142681995-142681995

stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.105delG; p.E37fs*14; 8:142681406-142681406

skin; breastmalignant_melanomaDeletion - Frameshift

c.285T>C; p.A95A; 8:142682072-142682072

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.285T>C; p.A95A; 8:142682072-142682072

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.285T>C; p.A95A; 8:142682072-142682072

thyroidother; neoplasmSubstitution - coding silent

c.136G>A; p.A46T; 8:142681923-142681923

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.224T>G; p.I75S; 8:142682011-142682011

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.326G>A; p.W109*; 8:142682113-142682113

large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.326G>A; p.W109*; 8:142682113-142682113

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.177G>A; p.L59L; 8:142681964-142681964

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.333C>T; p.P111P; 8:142682120-142682120

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.209T>C; p.V70A; 8:142681996-142681996

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.10T>C; p.L4L; 8:142680548-142680548

thyroidother; neoplasmSubstitution - coding silent

c.342C>A; p.L114L; 8:142682129-142682129

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.342C>A; p.L114L; 8:142682129-142682129

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.342C>A; p.L114L; 8:142682129-142682129

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.342C>A; p.L114L; 8:142682129-142682129

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.342C>A; p.L114L; 8:142682129-142682129

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.342C>A; p.L114L; 8:142682129-142682129

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.342C>A; p.L114L; 8:142682129-142682129

upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.342C>A; p.L114L; 8:142682129-142682129

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent