Colon Cancer: Gene >> HCCS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321143
Start	11112137:11112137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.77C>G
AA Mutation	p.Pro26Arg(p.P26R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321143
Start	11114939:11114939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.205A>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HCCS

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000321143
Start	11117267:11117267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752050558
CDS Mutation	c.253A>G
AA Mutation	p.Met85Val(p.M85V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321143
Start	11121754:11121754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751T>A
AA Mutation	p.Ser251Thr(p.S251T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321143
Start	11121740:11121740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.737G>A
AA Mutation	p.Arg246His(p.R246H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321143
Start	11114849:11114849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.115A>G
AA Mutation	p.Thr39Ala(p.T39A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript