Colon Cancer: Gene >> GCG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375497
Start	162144082:162144082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481A>C
AA Mutation	p.Asn161His(p.N161H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375497
Start	162149165:162149165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14A>G
AA Mutation	p.Tyr5Cys(p.Y5C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375497
Start	162147391:162147391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000375497
Start	162147381:162147381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226C>T
AA Mutation	p.Gln76Ter(p.Q76*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GCG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375497
Start	162144114:162144114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449C>A
AA Mutation	p.Ser150Tyr(p.S150Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375497
Start	162144155:162144155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202010736
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript