Colon Cancer: Gene >> NDRG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000570248
Start	58511443:58511443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370628261
CDS Mutation	c.926G>A
AA Mutation	p.Arg309His(p.R309H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000570248
Start	58504408:58504408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.298G>T
AA Mutation	p.Val100Leu(p.V100L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000570248
Start	58504185:58504185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760614649
CDS Mutation	c.159C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394282
Start	58487827:58487828(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.113dupG
AA Mutation	p.Gln39ProfsTer24(p.Q39Pfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NDRG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000570248
Start	58511500:58511500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983G>A
AA Mutation	p.Arg328His(p.R328H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000570248
Start	58511489:58511489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972G>T
Mutation Classification	Silent
Feature Type	Transcript