Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DEPTOR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286234
Start	120006866:120006866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.987G>T
AA Mutation	p.Lys329Asn(p.K329N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286234
Start	119929906:119929906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393G>T
AA Mutation	p.Lys131Asn(p.K131N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286234
Start	120006853:120006853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147092773
CDS Mutation	c.974C>T
AA Mutation	p.Pro325Leu(p.P325L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286234
Start	120003083:120003083(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.902delC
AA Mutation	p.Pro301LeufsTer10(p.P301Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000286234
Start	119928479:119928479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.202G>T
AA Mutation	p.Glu68Ter(p.E68*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DEPTOR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286234
Start	120002980:120002980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.794G>A
AA Mutation	p.Ser265Asn(p.S265N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286234
Start	119928447:119928447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170T>C
AA Mutation	p.Leu57Pro(p.L57P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286234
Start	119873907:119873907(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.64delG
AA Mutation	p.Ala22ArgfsTer48(p.A22Rfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript