Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GRB14

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263915
Start	164508470:164508470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200456570
CDS Mutation	c.1008G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263915
Start	164508826:164508826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762217333
CDS Mutation	c.843C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263915
Start	164493141:164493141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749661032
CDS Mutation	c.1518C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000263915
Start	164522063:164522063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.733G>T
AA Mutation	p.Glu245Ter(p.E245*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263915
Start	164497391:164497392(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1203dupA
AA Mutation	p.Glu402ArgfsTer18(p.E402Rfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GRB14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263915
Start	164493083:164493083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142669508
CDS Mutation	c.1576G>A
AA Mutation	p.Val526Ile(p.V526I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263915
Start	164497476:164497476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1119G>T
AA Mutation	p.Glu373Asp(p.E373D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263915
Start	164497481:164497481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1114T>C
AA Mutation	p.Ser372Pro(p.S372P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263915
Start	164497218:164497218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1287A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000263915
Start	164527073:164527073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.544G>T
AA Mutation	p.Glu182Ter(p.E182*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript