Colon Cancer: Gene >> CCR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296140
Start	46203268:46203268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1046A>G
AA Mutation	p.His349Arg(p.H349R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296140
Start	46203653:46203653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.661G>T
AA Mutation	p.Gly221Trp(p.G221W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296140
Start	46203769:46203769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545C>T
AA Mutation	p.Thr182Ile(p.T182I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296140
Start	46203469:46203469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.845C>T
AA Mutation	p.Ala282Val(p.A282V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296140
Start	46203916:46203916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398T>G
AA Mutation	p.Leu133Arg(p.L133R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296140
Start	46203470:46203470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.844G>A
AA Mutation	p.Ala282Thr(p.A282T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296140
Start	46203404:46203404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199658624
CDS Mutation	c.910G>A
AA Mutation	p.Val304Ile(p.V304I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296140
Start	46203529:46203529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.785C>A
AA Mutation	p.Ser262Tyr(p.S262Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296140
Start	46204245:46204245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760444180
CDS Mutation	c.69G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296140
Start	46203417:46203417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.897G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296140
Start	46203957:46203957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146488613
CDS Mutation	c.357C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296140
Start	46203876:46203876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146268408
CDS Mutation	c.438C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000296140
Start	46203629:46203629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Ter(p.R229*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CCR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296140
Start	46203538:46203538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.776T>A
AA Mutation	p.Ile259Lys(p.I259K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296140
Start	46203746:46203746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370179296
CDS Mutation	c.568G>A
AA Mutation	p.Glu190Lys(p.E190K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript