Colon Cancer: Gene >> CXCR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295683
Start	218164214:218164214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149021594
CDS Mutation	c.998G>A
AA Mutation	p.Arg333His(p.R333H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295683
Start	218164358:218164358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140803476
CDS Mutation	c.854G>A
AA Mutation	p.Arg285Gln(p.R285Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295683
Start	218164781:218164781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431G>A
AA Mutation	p.Arg144His(p.R144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295683
Start	218164280:218164280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932A>C
AA Mutation	p.Asn311Thr(p.N311T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295683
Start	218165188:218165188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.24G>T
AA Mutation	p.Gln8His(p.Q8H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295683
Start	218164376:218164376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56030518
CDS Mutation	c.836G>A
AA Mutation	p.Arg279His(p.R279H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295683
Start	218164426:218164426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.786G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295683
Start	218165167:218165167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.45A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CXCR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295683
Start	218164923:218164923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289G>A
AA Mutation	p.Ala97Thr(p.A97T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295683
Start	218165113:218165113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99A>C
AA Mutation	p.Glu33Asp(p.E33D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript