Colon Cancer: Gene >> NAT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286479
Start	18400163:18400163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>A
AA Mutation	p.Ala54Thr(p.A54T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286479
Start	18400403:18400403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752501077
CDS Mutation	c.400C>T
AA Mutation	p.Pro134Ser(p.P134S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286479
Start	18400093:18400093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NAT2

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286479
Start	18400447:18400448(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.445dupA
AA Mutation	p.Ile149AsnfsTer29(p.I149Nfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript