Colon Cancer: Gene >> CCR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292301
Start	46358417:46358417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890A>T
AA Mutation	p.His297Leu(p.H297L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292301
Start	46358144:46358144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617G>T
AA Mutation	p.Arg206Met(p.R206M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292301
Start	46357703:46357703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.176G>C
AA Mutation	p.Gly59Ala(p.G59A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292301
Start	46359838:46359838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1103T>G
AA Mutation	p.Leu368Arg(p.L368R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000292301
Start	46359679:46359679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.944T>G
AA Mutation	p.Leu315Arg(p.L315R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292301
Start	46358141:46358141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771654222
CDS Mutation	c.614T>C
AA Mutation	p.Met205Thr(p.M205T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292301
Start	46358415:46358415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292301
Start	46357719:46357719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292301
Start	46357893:46357893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292301
Start	46358448:46358448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.921C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292301
Start	46357935:46357935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781525332
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000292301
Start	46358224:46358224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.697C>T
AA Mutation	p.Arg233Ter(p.R233*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CCR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292301
Start	46358225:46358225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539087679
CDS Mutation	c.698G>A
AA Mutation	p.Arg233Gln(p.R233Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292301
Start	46359789:46359789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368150580
CDS Mutation	c.1054G>A
AA Mutation	p.Asp352Asn(p.D352N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292301
Start	46358084:46358084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.557C>A
AA Mutation	p.Ser186Tyr(p.S186Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292301
Start	46357638:46357638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.111G>T
Mutation Classification	Silent
Feature Type	Transcript