Colon Cancer: Gene >> CMKLR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312143
Start	108292211:108292211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750358962
CDS Mutation	c.752G>A
AA Mutation	p.Arg251His(p.R251H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312143
Start	108292719:108292719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.244G>A
AA Mutation	p.Ala82Thr(p.A82T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312143
Start	108292065:108292065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.898C>A
AA Mutation	p.Leu300Met(p.L300M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312143
Start	108292680:108292680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.283C>A
AA Mutation	p.His95Asn(p.H95N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312143
Start	108292695:108292695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268G>A
AA Mutation	p.Val90Ile(p.V90I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312143
Start	108292039:108292039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312143
Start	108292275:108292275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.688C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312143
Start	108292252:108292252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000312143
Start	108292354:108292354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609G>A
AA Mutation	p.Trp203Ter(p.W203*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000312143
Start	108292147:108292147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816C>A
AA Mutation	p.Cys272Ter(p.C272*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CMKLR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312143
Start	108291898:108291898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1065G>T
AA Mutation	p.Lys355Asn(p.K355N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312143
Start	108292665:108292665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370635582
CDS Mutation	c.298G>A
AA Mutation	p.Ala100Thr(p.A100T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312143
Start	108292228:108292228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.735C>G
AA Mutation	p.Cys245Trp(p.C245W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312143
Start	108292229:108292229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.734G>T
AA Mutation	p.Cys245Phe(p.C245F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312143
Start	108291895:108291895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1068G>A
AA Mutation	p.Met356Ile(p.M356I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript