Colon Cancer: Gene >> EXOG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287675
Start	38496459:38496459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.92C>A
AA Mutation	p.Ala31Asp(p.A31D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000287675
Start	38501453:38501453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756034502
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Ter(p.R138*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EXOG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287675
Start	38524214:38524214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570781004
CDS Mutation	c.959G>A
AA Mutation	p.Arg320Gln(p.R320Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287675
Start	38501480:38501480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.439A>C
AA Mutation	p.Asn147His(p.N147H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000287675
Start	38523902:38523902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.647T>C
AA Mutation	p.Val216Ala(p.V216A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287675
Start	38501482:38501482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript