Colon Cancer: Gene >> NDRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323851
Start	133262066:133262066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374160497
CDS Mutation	c.307G>A
AA Mutation	p.Ala103Thr(p.A103T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323851
Start	133256808:133256808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506C>T
AA Mutation	p.Ala169Val(p.A169V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323851
Start	133239084:133239084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.979C>T
AA Mutation	p.Arg327Cys(p.R327C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323851
Start	133250503:133250503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.635G>A
AA Mutation	p.Arg212His(p.R212H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323851
Start	133262147:133262147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.226C>A
AA Mutation	p.Leu76Ile(p.L76I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323851
Start	133238953:133238953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323851
Start	133248738:133248738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532191834
CDS Mutation	c.732G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NDRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323851
Start	133264640:133264640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112G>A
AA Mutation	p.Glu38Lys(p.E38K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript