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

Basic Information

Gene ID

389421

Name

LIN28B

Synonymous

lin-28 homolog B (C. elegans);LIN28B;lin-28 homolog B (C. elegans)

Definition

Lin-28.2|lin-28B|protein lin-28 homolog B

Position

6q21

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.447G>T; p.K149N; 6:105078477-105078477

 breastcarcinomaSubstitution - Missense

c.437C>T; p.P146L; 6:105078467-105078467

 breastcarcinomaSubstitution - Missense

c.558A>T; p.P186P; 6:105078588-105078588

 breastcarcinomaSubstitution - coding silent

c.135C>A; p.F45L; 6:104958223-104958223

 breastcarcinomaSubstitution - Missense

c.728C>G; p.S243*; 6:105078758-105078758

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.13G>A; p.G5R; 6:104958101-104958101

 kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - Missense

c.223A>T; p.R75*; 6:105026322-105026322

 kidneyother; neoplasmSubstitution - Nonsense

c.42C>G; p.P14P; 6:104958130-104958130

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.160A>C; p.S54R; 6:104958248-104958248

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.581A>G; p.E194G; 6:105078611-105078611

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.650G>A; p.R217Q; 6:105078680-105078680

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.724C>T; p.P242S; 6:105078754-105078754

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.534A>C; p.G178G; 6:105078564-105078564

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.52C>T; p.P18S; 6:104958140-104958140

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.52C>T; p.P18S; 6:104958140-104958140

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.663A>T; p.S221S; 6:105078693-105078693

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.487A>T; p.N163Y; 6:105078517-105078517

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.301G>T; p.G101*; 6:105026400-105026400

 livercarcinoma; hepatocellular_carcinomaSubstitution - Nonsense

c.681C>A; p.S227S; 6:105078711-105078711

 lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.181G>A; p.D61N; 6:104958269-104958269

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.31G>T; p.G11*; 6:104958119-104958119

 lungcarcinoma; adenocarcinomaSubstitution - Nonsense

c.97C>A; p.H33N; 6:104958185-104958185

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.409C>A; p.H137N; 6:105078439-105078439

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.611C>A; p.P204Q; 6:105078641-105078641

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.10G>A; p.G4S; 6:104957260-104957260

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.531G>T; p.Q177H; 6:105078561-105078561

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.453C>T; p.C151C; 6:105078483-105078483

 oesophaguscarcinomaSubstitution - coding silent

c.475C>T; p.H159Y; 6:105078505-105078505

 oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.564T>C; p.T188T; 6:105078594-105078594

 oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - coding silent

c.437C>T; p.P146L; 6:105078467-105078467

 ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.295G>T; p.V99L; 6:105026394-105026394

 pancreascarcinomaSubstitution - Missense

c.131G>T; p.G44V; 6:104958219-104958219

 prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.125G>A; p.G42E; 6:104958213-104958213

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.347G>A; p.G116E; 6:105026446-105026446

 skinmalignant_melanomaSubstitution - Missense

c.308G>C; p.G103A; 6:105026407-105026407

 skinmalignant_melanomaSubstitution - Missense

c.533G>A; p.G178E; 6:105078563-105078563

 skinmalignant_melanomaSubstitution - Missense

c.684G>A; p.T228T; 6:105078714-105078714

 skinmalignant_melanomaSubstitution - coding silent

c.684G>A; p.T228T; 6:105078714-105078714

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.566C>T; p.S189L; 6:105078596-105078596

 skinmalignant_melanomaSubstitution - Missense

c.335G>A; p.R112K; 6:105026434-105026434

 skinmalignant_melanomaSubstitution - Missense

c.123G>A; p.M41I; 6:104958211-104958211

 skinmalignant_melanomaSubstitution - Missense

c.217G>A; p.G73R; 6:105026316-105026316

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.547G>C; p.E183Q; 6:105078577-105078577

 skinmalignant_melanomaSubstitution - Missense

c.465G>A; p.Q155Q; 6:105078495-105078495

 skinmalignant_melanomaSubstitution - coding silent

c.250G>A; p.E84K; 6:105026349-105026349

 skinmalignant_melanomaSubstitution - Missense

c.740G>A; p.R247K; 6:105078770-105078770

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.721G>C; p.G241R; 6:105078751-105078751

 skinmalignant_melanomaSubstitution - Missense

c.294G>A; p.R98R; 6:105026393-105026393

 skinmalignant_melanomaSubstitution - coding silent

c.586G>A; p.G196R; 6:105078616-105078616

 skinmalignant_melanomaSubstitution - Missense

c.362A>T; p.K121I; 6:105026461-105026461

 skinmalignant_melanomaSubstitution - Missense

c.13G>A; p.G5R; 6:104958101-104958101

 skinmalignant_melanomaSubstitution - Missense

c.57G>A; p.E19E; 6:104958145-104958145

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.591C>T; p.G197G; 6:105078621-105078621

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.570T>C; p.T190T; 6:105078600-105078600

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent