Colon Cancer: Gene >> NAT9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357814
Start	74772233:74772233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379G>A
AA Mutation	p.Ala127Thr(p.A127T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357814
Start	74772218:74772218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746674904
CDS Mutation	c.394G>A
AA Mutation	p.Gly132Arg(p.G132R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357814
Start	74771802:74771802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780397329
CDS Mutation	c.546C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NAT9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357814
Start	74773579:74773579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187G>T
AA Mutation	p.Asp63Tyr(p.D63Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript