Colon Cancer: Gene >> CD200

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000473539
Start	112347806:112347806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759192172
CDS Mutation	c.745G>A
AA Mutation	p.Asp249Asn(p.D249N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000473539
Start	112347587:112347587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526T>C
AA Mutation	p.Phe176Leu(p.F176L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000473539
Start	112347766:112347766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.705G>T
AA Mutation	p.Lys235Asn(p.K235N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000473539
Start	112347589:112347589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202184567
CDS Mutation	c.528C>A
AA Mutation	p.Phe176Leu(p.F176L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000473539
Start	112345230:112345230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.438T>G
AA Mutation	p.Cys146Trp(p.C146W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000473539
Start	112335965:112335965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35G>C
AA Mutation	p.Gly12Ala(p.G12A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000473539
Start	112345047:112345047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.255C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000473539
Start	112345228:112345229(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.436_437insTTTCTG
AA Mutation	p.Cys146delinsPheSerGly(p.C146delinsFSG)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CD200

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000473539
Start	112347630:112347630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759307241
CDS Mutation	c.569G>A
AA Mutation	p.Arg190His(p.R190H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000473539
Start	112347782:112347782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748502402
CDS Mutation	c.721G>T
AA Mutation	p.Val241Leu(p.V241L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000473539
Start	112349765:112349765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.823C>T
AA Mutation	p.Leu275Phe(p.L275F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript