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Pediatric cancer database
General information | Literature | Expression | Regulation | Variant | Interaction

Basic Information

Gene ID

7298

Name

TYMS

Synonymous

HST422|TMS|TS;thymidylate synthetase;TYMS;thymidylate synthetase

Definition

TSase|thymidylate synthase

Position

18p11.32

Gene Type

protein-coding

Gene Mutation:

PCGP germline mutation
PCGP somatic mutation
COSMIC somatic mutation

PCGP germline mutation   [Top]

There is no record for TYMS

PCGP somatic mutation   [Top]

Variant (Variant; Chr; Position)

Genotype (MutationType; MutationClass; ReferenceAllele; Genotype; Origin)

Disease (CancerType; ValidationStatus; SequencingType)

TYMS_G143R; chr18; 662293

SUB; MISSENSE; G; G/A; SOMATICRHB; VALID; WGS

TYMS_G143R; chr18; 662293

SUB; MISSENSE; G; G/A; SOMATICRHB; VALID; WGS

TYMS_G143R; chr18; 662293

SUB; MISSENSE; G; G/A; SOMATICRHB; VALID; WGS

TYMS_G143R; chr18; 662293

SUB; MISSENSE; G; G/A; SOMATICRHB; PUTATIVE-HQ; EXOME

TYMS_G143R; chr18; 662293

SUB; MISSENSE; G; G/A; SOMATICRHB; PUTATIVE-HQ; WGS

TYMS_G143R; chr18; 662293

SUB; MISSENSE; G; G/A; SOMATICRHB; PUTATIVE-HQ; EXOME

TYMS_G143R; chr18; 662293

SUB; MISSENSE; G; G/A; SOMATICRHB; PUTATIVE-HQ; WGS

TYMS_G143R; chr18; 662293

SUB; MISSENSE; G; G/A; SOMATICRHB; PUTATIVE-HQ; EXOME

TYMS_G143R; chr18; 662293

SUB; MISSENSE; G; G/A; SOMATICRHB; PUTATIVE-HQ; WGS

COSMIC somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

c.494T>C; p.I165T;

livercarcinoma; hepatocellular_carcinoma

c.125G>T; p.R42L;

oesophaguscarcinoma; adenocarcinoma

c.812G>A; p.R271Q;

oesophaguscarcinoma; adenocarcinoma

c.425T>G; p.F142C;

large_intestine; coloncarcinoma; adenocarcinoma

c.603C>A; p.F201L;

large_intestine; coloncarcinoma; adenocarcinoma

c.572C>T; p.A191V;

livercarcinoma

c.572C>T; p.A191V;

livercarcinoma

c.889C>G; p.Q297E;

lungcarcinoma; adenocarcinoma

c.811C>T; p.R271*;

endometriumcarcinoma; serous_carcinoma

c.445A>G; p.M149V;

lungcarcinoma; adenocarcinoma

c.594C>G; p.L198L;

lungcarcinoma; adenocarcinoma

c.663C>T; p.L221L;

lung; right_upper_lobecarcinoma; adenocarcinoma

c.519C>T; p.D173D;

large_intestine; coloncarcinoma; adenocarcinoma

c.902A>G; p.Y301C;

large_intestine; caecumcarcinoma; adenocarcinoma

c.687C>G; p.S229R;

large_intestine; coloncarcinoma; adenocarcinoma

c.847C>T; p.R283*;

large_intestine; rectumcarcinoma; adenocarcinoma

c.527G>A; p.R176K;

large_intestine; rectumcarcinoma; adenocarcinoma

c.636G>A; p.L212L;

large_intestine; caecumcarcinoma; adenocarcinoma

c.619G>A; p.E207K;

urinary_tract; bladdercarcinoma

c.612G>A; p.V204V;

urinary_tract; bladdercarcinoma

c.700A>G; p.T234A;

large_intestine; coloncarcinoma; adenocarcinoma

c.634C>T; p.L212L;

large_intestine; caecumcarcinoma; adenocarcinoma

c.681C>T; p.I227I;

endometriumcarcinoma; endometrioid_carcinoma

c.604T>C; p.Y202H;

breastcarcinoma

c.197G>A; p.S66N;

large_intestine; caecumcarcinoma; adenocarcinoma

c.692_693CC>AT; p.A231D;

skinmalignant_melanoma

c.259G>A; p.E87K;

skinmalignant_melanoma


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