Colon Cancer: Gene >> SMR3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226460
Start	70366795:70366795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751646049
CDS Mutation	c.206C>A
AA Mutation	p.Pro69Gln(p.P69Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226460
Start	70366852:70366852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263G>T
AA Mutation	p.Arg88Ile(p.R88I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226460
Start	70366849:70366849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.260G>A
AA Mutation	p.Gly87Glu(p.G87E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226460
Start	70366885:70366885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.296G>A
AA Mutation	p.Gly99Asp(p.G99D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SMR3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226460
Start	70366852:70366852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263G>T
AA Mutation	p.Arg88Ile(p.R88I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226460
Start	70366715:70366715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126T>C
Mutation Classification	Silent
Feature Type	Transcript