Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CXCR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318507
Start	218135864:218135864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1063C>A
AA Mutation	p.His355Asn(p.H355N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318507
Start	218135105:218135105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.304C>T
AA Mutation	p.Pro102Ser(p.P102S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318507
Start	218135794:218135794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.993A>G
AA Mutation	p.Ile331Met(p.I331M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318507
Start	218134818:218134818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.17T>C
AA Mutation	p.Met6Thr(p.M6T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318507
Start	218135293:218135293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492C>A
AA Mutation	p.Phe164Leu(p.F164L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000318507
Start	218135376:218135376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.575T>G
AA Mutation	p.Val192Gly(p.V192G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CXCR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318507
Start	218134859:218134859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
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	ENST00000318507
Start	218135293:218135293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492C>A
AA Mutation	p.Phe164Leu(p.F164L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318507
Start	218135469:218135469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668C>A
AA Mutation	p.Pro223Gln(p.P223Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318507
Start	218135134:218135134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333C>A
Mutation Classification	Silent
Feature Type	Transcript