Colon Cancer: Gene >> DTX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337737
Start	57607590:57607590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201091006
CDS Mutation	c.727G>A
AA Mutation	p.Val243Ile(p.V243I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337737
Start	57607421:57607421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.558G>T
AA Mutation	p.Glu186Asp(p.E186D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337737
Start	57607314:57607314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752141567
CDS Mutation	c.451C>T
AA Mutation	p.Pro151Ser(p.P151S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337737
Start	57607568:57607568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200246539
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337737
Start	57607187:57607187(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.329delG
AA Mutation	p.Gly110ValfsTer86(p.G110Vfs*86)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DTX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337737
Start	57607020:57607020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157G>A
AA Mutation	p.Glu53Lys(p.E53K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337737
Start	57608624:57608624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376657147
CDS Mutation	c.855G>A
Mutation Classification	Silent
Feature Type	Transcript