Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> OGN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262551
Start	92403365:92403365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43C>T
AA Mutation	p.Pro15Ser(p.P15S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262551
Start	92390039:92390039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764235963
CDS Mutation	c.445G>A
AA Mutation	p.Asp149Asn(p.D149N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262551
Start	92390005:92390005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479A>T
AA Mutation	p.Asp160Val(p.D160V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262551
Start	92393199:92393199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314A>G
AA Mutation	p.Tyr105Cys(p.Y105C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262551
Start	92390040:92390040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754036150
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OGN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262551
Start	92389942:92389942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542A>C
AA Mutation	p.Lys181Thr(p.K181T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262551
Start	92386249:92386249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.678A>C
AA Mutation	p.Glu226Asp(p.E226D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262551
Start	92390039:92390039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764235963
CDS Mutation	c.445G>A
AA Mutation	p.Asp149Asn(p.D149N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript