Colon Cancer: Gene >> GTF3A

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381140
Start	27429871:27429871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.304T>A
AA Mutation	p.Cys102Ser(p.C102S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381140
Start	27435177:27435177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918G>T
AA Mutation	p.Lys306Asn(p.K306N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381140
Start	27435473:27435473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974T>G
AA Mutation	p.Leu325Arg(p.L325R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381140
Start	27434145:27434145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569T>C
AA Mutation	p.Val190Ala(p.V190A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381140
Start	27434825:27434825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664T>C
AA Mutation	p.Cys222Arg(p.C222R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GTF3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381140
Start	27435177:27435177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918G>T
AA Mutation	p.Lys306Asn(p.K306N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript