Colon Cancer: Gene >> CD200R1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000471858
Start	112925149:112925149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745A>G
AA Mutation	p.Ile249Val(p.I249V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000471858
Start	112928989:112928989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377071470
CDS Mutation	c.527C>T
AA Mutation	p.Ala176Val(p.A176V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000471858
Start	112929439:112929439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202A>C
AA Mutation	p.Asn68His(p.N68H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000471858
Start	112929436:112929436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.205T>G
AA Mutation	p.Leu69Val(p.L69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000471858
Start	112931136:112931136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.103A>C
AA Mutation	p.Thr35Pro(p.T35P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000471858
Start	112924509:112924509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836C>A
AA Mutation	p.Ser279Tyr(p.S279Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000471858
Start	112923785:112923785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.870C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000471858
Start	112929500:112929500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.141T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CD200R1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000471858
Start	112929028:112929028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200448544
CDS Mutation	c.488G>T
AA Mutation	p.Arg163Ile(p.R163I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000471858
Start	112974841:112974841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.17G>T
AA Mutation	p.Arg6Ile(p.R6I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000471858
Start	112929214:112929214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550063106
CDS Mutation	c.427C>T
AA Mutation	p.Arg143Cys(p.R143C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000471858
Start	112931123:112931123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146696278
CDS Mutation	c.116C>T
AA Mutation	p.Ser39Leu(p.S39L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript