Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> AGPS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264167
Start	177462012:177462012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990G>T
AA Mutation	p.Glu330Asp(p.E330D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264167
Start	177445603:177445603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.847A>T
AA Mutation	p.Thr283Ser(p.T283S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264167
Start	177538077:177538077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1859G>A
AA Mutation	p.Gly620Asp(p.G620D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264167
Start	177436867:177436867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545G>A
AA Mutation	p.Arg182Gln(p.R182Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264167
Start	177434378:177434378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264167
Start	177462006:177462006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.984T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264167
Start	177497719:177497719(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1320delT
AA Mutation	p.Phe440LeufsTer8(p.F440Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AGPS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264167
Start	177437028:177437028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611G>A
AA Mutation	p.Arg204Gln(p.R204Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264167
Start	177493186:177493186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1272G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264167
Start	177499709:177499710(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1475+7_1475+8insAATATCATACACTTGATATTGCTGCAAAATTTGGGTATGGC
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript