Colon Cancer: Gene >> OAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368845
Start	124398082:124398082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121965054
CDS Mutation	c.1180T>C
AA Mutation	p.Cys394Arg(p.C394R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368845
Start	124403829:124403829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140966644
CDS Mutation	c.740T>C
AA Mutation	p.Met247Thr(p.M247T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368845
Start	124398012:124398012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121965044
CDS Mutation	c.1250C>T
AA Mutation	p.Pro417Leu(p.P417L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368845
Start	124398074:124398074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1188A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368845
Start	124412075:124412075(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.97delA
AA Mutation	p.Thr33GlnfsTer28(p.T33Qfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> OAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368845
Start	124400977:124400977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1022A>G
AA Mutation	p.Glu341Gly(p.E341G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368845
Start	124412075:124412075(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.97delA
AA Mutation	p.Thr33GlnfsTer28(p.T33Qfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript