Colon Cancer: Gene >> TRIT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316891
Start	39844569:39844569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078C>A
AA Mutation	p.Leu360Ile(p.L360I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316891
Start	39883443:39883443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.49A>T
AA Mutation	p.Arg17Trp(p.R17W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000316891
Start	39848095:39848095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706C>A
AA Mutation	p.Leu236Ile(p.L236I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316891
Start	39844160:39844160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1175G>T
AA Mutation	p.Arg392Ile(p.R392I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316891
Start	39850158:39850158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664T>C
AA Mutation	p.Ser222Pro(p.S222P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316891
Start	39841900:39841900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1248C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316891
Start	39852862:39852862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.429C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316891
Start	39844630:39844630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1017C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316891
Start	39844549:39844549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs16826617
CDS Mutation	c.1098C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316891
Start	39847225:39847225(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1001delT
AA Mutation	p.Leu334Ter(p.L334*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRIT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316891
Start	39852842:39852842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777502421
CDS Mutation	c.449G>A
AA Mutation	p.Arg150Gln(p.R150Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript