Colon Cancer: Gene >> TRDMT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377799
Start	17168876:17168876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216G>T
AA Mutation	p.Met72Ile(p.M72I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377799
Start	17161523:17161523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776907517
CDS Mutation	c.349C>A
AA Mutation	p.Leu117Ile(p.L117I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377799
Start	17157537:17157537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.791A>G
AA Mutation	p.Asn264Ser(p.N264S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377799
Start	17162201:17162201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138454921
CDS Mutation	c.288G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377799
Start	17153523:17153523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1059A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TRDMT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377799
Start	17149104:17149104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1112G>A
AA Mutation	p.Arg371His(p.R371H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377799
Start	17168881:17168881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371526424
CDS Mutation	c.211G>A
AA Mutation	p.Asp71Asn(p.D71N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377799
Start	17157701:17157701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745653840
CDS Mutation	c.627C>T
Mutation Classification	Silent
Feature Type	Transcript