Colon Cancer: Gene >> PGF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000405431
Start	74948519:74948519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764795497
CDS Mutation	c.380G>A
AA Mutation	p.Arg127His(p.R127H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405431
Start	74948524:74948524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749171908
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405431
Start	74942730:74942730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576817206
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405431
Start	74955198:74955198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751945485
CDS Mutation	c.45C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PGF

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405431
Start	74949411:74949411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201159181
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript