Colon Cancer: Gene >> HBA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320868
Start	177373:177373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.391G>A
AA Mutation	p.Ala131Thr(p.A131T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320868
Start	177310:177310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328C>A
AA Mutation	p.Leu110Met(p.L110M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320868
Start	176723:176723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320868
Start	177097:177097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HBA1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320868
Start	176722:176722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6G>A
Mutation Classification	Silent
Feature Type	Transcript