Colon Cancer: Gene >> NAT8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272425
Start	73641259:73641259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370G>T
AA Mutation	p.Ala124Ser(p.A124S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272425
Start	73641312:73641312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317G>A
AA Mutation	p.Gly106Asp(p.G106D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272425
Start	73641042:73641042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146559874
CDS Mutation	c.587C>T
AA Mutation	p.Thr196Met(p.T196M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272425
Start	73641562:73641562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555774069
CDS Mutation	c.67C>T
AA Mutation	p.Arg23Trp(p.R23W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000272425
Start	73641543:73641543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754121016
CDS Mutation	c.86C>T
AA Mutation	p.Ala29Val(p.A29V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272425
Start	73641380:73641380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149442492
CDS Mutation	c.249G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272425
Start	73641122:73641122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NAT8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272425
Start	73641457:73641457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172G>A
AA Mutation	p.Gly58Arg(p.G58R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript