Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GREM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318160
Start	240493252:240493252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224C>T
AA Mutation	p.Thr75Met(p.T75M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318160
Start	240493139:240493139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>A
AA Mutation	p.Glu113Lys(p.E113K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318160
Start	240493115:240493115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>A
AA Mutation	p.Ala121Thr(p.A121T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318160
Start	240493391:240493391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85G>A
AA Mutation	p.Ala29Thr(p.A29T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318160
Start	240493011:240493011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.465C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000318160
Start	240493341:240493341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.135G>A
AA Mutation	p.Trp45Ter(p.W45*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318160
Start	240493030:240493031(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.445dupA
AA Mutation	p.Ile149AsnfsTer66(p.I149Nfs*66)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GREM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318160
Start	240493252:240493252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224C>T
AA Mutation	p.Thr75Met(p.T75M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript