Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> OAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000202917
Start	112911104:112911104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148820389
CDS Mutation	c.523G>A
AA Mutation	p.Glu175Lys(p.E175K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000202917
Start	112919422:112919422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1072G>A
AA Mutation	p.Asp358Asn(p.D358N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000202917
Start	112917596:112917596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934G>T
AA Mutation	p.Asp312Tyr(p.D312Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202917
Start	112908796:112908796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202917
Start	112911160:112911160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.579A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000202917
Start	112916689:112916689(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.839delA
AA Mutation	p.Asn280ThrfsTer8(p.N280Tfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> OAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000202917
Start	112907097:112907097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58C>A
AA Mutation	p.Leu20Ile(p.L20I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000202917
Start	112917668:112917668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1006G>A
AA Mutation	p.Asp336Asn(p.D336N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000202917
Start	112907167:112907167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128A>G
AA Mutation	p.Glu43Gly(p.E43G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript