Colon Cancer: Gene >> PDRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000202017
Start	31948859:31948859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187A>G
AA Mutation	p.Asn63Asp(p.N63D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000202017
Start	31948818:31948818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.228G>T
AA Mutation	p.Met76Ile(p.M76I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000202017
Start	31945851:31945851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358A>G
AA Mutation	p.Asn120Asp(p.N120D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202017
Start	31946536:31946536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.279G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PDRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000202017
Start	31951930:31951930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755286962
CDS Mutation	c.32G>A
AA Mutation	p.Arg11Gln(p.R11Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript