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Gene information | Literature | Expression | lncRNA | Mutation | Homolog

Basic Information

Gene ID

79727

Name

LIN28A

Synonymous

lin-28 homolog A (C. elegans);LIN28A;lin-28 homolog A (C. elegans)

Definition

RNA-binding protein LIN-28|protein lin-28 homolog A|zinc finger CCHC domain-containing protein 1|zinc finger, CCHC domain containing 1

Position

1p36.11

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.50C>A; p.A17E; 1:26411404-26411404

 breastcarcinomaSubstitution - Missense

c.125G>A; p.G42D; 1:26411479-26411479

 central_nervous_system; braingliomaSubstitution - Missense

c.518C>G; p.S173*; 1:26426346-26426346

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.387G>A; p.M129I; 1:26425461-26425461

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.574C>T; p.R192*; 1:26426402-26426402

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.11T>C; p.V4A; 1:26410902-26410902

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.25delT; p.F9fs*50; 1:26410916-26410916

 haematopoietic_and_lymphoid_tissue; spleenlymphoid_neoplasm; marginal_zone_lymphomaDeletion - Frameshift

c.201delC; p.P69fs*19; 1:26411555-26411555

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.148C>T; p.R50C; 1:26411502-26411502

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.297G>C; p.K99N; 1:26425371-26425371

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.439C>A; p.H147N; 1:26426267-26426267

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.415T>A; p.C139S; 1:26426243-26426243

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.186C>T; p.A62A; 1:26411540-26411540

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.159C>T; p.F53F; 1:26411513-26411513

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.574C>T; p.R192*; 1:26426402-26426402

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.126C>T; p.G42G; 1:26411480-26411480

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.98A>G; p.D33G; 1:26411452-26411452

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.122C>T; p.A41V; 1:26411476-26411476

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.226-7C>T; p.?; 1:26425293-26425293

 livercarcinomaUnknown

c.226-7C>T; p.?; 1:26425293-26425293

 livercarcinomaUnknown

c.615G>A; p.P205P; 1:26426443-26426443

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.194C>T; p.A65V; 1:26411548-26411548

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.335C>T; p.P112L; 1:26425409-26425409

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.123G>A; p.A41A; 1:26411477-26411477

 oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - coding silent

c.85G>A; p.A29T; 1:26411439-26411439

 pancreascarcinomaSubstitution - Missense

c.614C>A; p.P205Q; 1:26426442-26426442

 prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.606C>T; p.T202T; 1:26426434-26426434

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.616G>A; p.E206K; 1:26426444-26426444

 skinmalignant_melanomaSubstitution - Missense

c.312G>A; p.L104L; 1:26425386-26425386

 skinmalignant_melanomaSubstitution - coding silent

c.629G>A; p.*210*; 1:26426457-26426457

 skinmalignant_melanomaSubstitution - coding silent

c.601C>T; p.P201S; 1:26426429-26426429

 skinmalignant_melanomaSubstitution - Missense

c.355G>A; p.G119R; 1:26425429-26425429

 skinmalignant_melanomaSubstitution - Missense

c.570C>T; p.Y190Y; 1:26426398-26426398

 skinmalignant_melanomaSubstitution - coding silent

c.436G>A; p.D146N; 1:26426264-26426264

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.377G>A; p.G126E; 1:26425451-26425451

 skinmalignant_melanomaSubstitution - Missense

c.377G>A; p.G126E; 1:26425451-26425451

 skinmalignant_melanomaSubstitution - Missense

c.253C>T; p.R85W; 1:26425327-26425327

 skinmalignant_melanomaSubstitution - Missense

c.504C>T; p.S168S; 1:26426332-26426332

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.624G>T; p.Q208H; 1:26426452-26426452

 stomachcarcinoma; diffuse_adenocarcinomaSubstitution - Missense

c.369G>A; p.R123R; 1:26425443-26425443

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.330C>T; p.T110T; 1:26425404-26425404

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.442C>T; p.H148Y; 1:26426270-26426270

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.567C>G; p.T189T; 1:26426395-26426395

 urinary_tract; bladdercarcinomaSubstitution - coding silent