Colon Cancer: Gene >> HELT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000515777
Start	185020474:185020474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431A>T
AA Mutation	p.Asp144Val(p.D144V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000515777
Start	185020719:185020719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676G>A
AA Mutation	p.Ala226Thr(p.A226T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000515777
Start	185020392:185020392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349C>T
AA Mutation	p.Arg117Cys(p.R117C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515777
Start	185020460:185020460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HELT

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000515777
Start	185020286:185020286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772210049
CDS Mutation	c.243G>A
Mutation Classification	Silent
Feature Type	Transcript