Colon Cancer: Gene >> CA10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285273
Start	51931041:51931041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.228G>T
AA Mutation	p.Met76Ile(p.M76I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285273
Start	51633609:51633609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831G>C
AA Mutation	p.Gln277His(p.Q277H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285273
Start	51633637:51633637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146043972
CDS Mutation	c.803G>A
AA Mutation	p.Arg268His(p.R268H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CA10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285273
Start	51635927:51635927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717G>T
AA Mutation	p.Met239Ile(p.M239I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285273
Start	52157738:52157738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49G>A
AA Mutation	p.Val17Ile(p.V17I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000285273
Start	51653691:51653691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511G>T
AA Mutation	p.Glu171Ter(p.E171*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript