Colon Cancer: Gene >> TIRAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392679
Start	126292779:126292779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370A>G
AA Mutation	p.Thr124Ala(p.T124A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000392679
Start	126293053:126293053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185114125
CDS Mutation	c.644G>A
AA Mutation	p.Arg215His(p.R215H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392679
Start	126292790:126292790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769940334
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392679
Start	126292604:126292604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371062583
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392679
Start	126292958:126292958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.549C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392679
Start	126292893:126292893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TIRAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392679
Start	126292945:126292945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.536T>A
AA Mutation	p.Leu179Gln(p.L179Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript