Colon Cancer: Gene >> NDRG2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298687
Start	21021858:21021858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298687
Start	21022408:21022408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769551465
CDS Mutation	c.207C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298687
Start	21023304:21023304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000298687
Start	21023294:21023294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.22C>T
AA Mutation	p.Gln8Ter(p.Q8*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000298687
Start	21023258:21023259(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.57_58insTTAGAATAAGATCAGT
AA Mutation	p.Thr20LeufsTer3(p.T20Lfs*3)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NDRG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298687
Start	21022886:21022886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750572401
CDS Mutation	c.95G>A
AA Mutation	p.Arg32Gln(p.R32Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298687
Start	21022127:21022127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279G>T
AA Mutation	p.Gln93His(p.Q93H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298687
Start	21021834:21021834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370648416
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript