Colon Cancer: Gene >> TRIB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311922
Start	125433501:125433501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545C>T
AA Mutation	p.Ala182Val(p.A182V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311922
Start	125436143:125436143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791C>A
AA Mutation	p.Ala264Asp(p.A264D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311922
Start	125436275:125436275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756032753
CDS Mutation	c.923C>T
AA Mutation	p.Ser308Phe(p.S308F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311922
Start	125436391:125436391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776955393
CDS Mutation	c.1039A>G
AA Mutation	p.Ile347Val(p.I347V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311922
Start	125436097:125436097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745G>A
AA Mutation	p.Val249Met(p.V249M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311922
Start	125436270:125436270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757119456
CDS Mutation	c.918C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311922
Start	125433373:125433373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311922
Start	125433535:125433535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774222003
CDS Mutation	c.579C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TRIB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311922
Start	125436299:125436299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138022510
CDS Mutation	c.947G>A
AA Mutation	p.Arg316His(p.R316H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311922
Start	125436420:125436420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1068G>T
AA Mutation	p.Gln356His(p.Q356H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript