Colon Cancer: Gene >> CD33

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262262
Start	51225572:51225572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.392C>A
AA Mutation	p.Ser131Tyr(p.S131Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262262
Start	51225365:51225365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144102805
CDS Mutation	c.185G>A
AA Mutation	p.Arg62Gln(p.R62Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262262
Start	51225476:51225476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296A>T
AA Mutation	p.Asn99Ile(p.N99I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262262
Start	51225934:51225934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550C>T
AA Mutation	p.Pro184Ser(p.P184S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262262
Start	51225502:51225502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150563546
CDS Mutation	c.322G>A
AA Mutation	p.Ala108Thr(p.A108T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262262
Start	51225836:51225836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.452G>A
AA Mutation	p.Gly151Asp(p.G151D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262262
Start	51226075:51226075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748041775
CDS Mutation	c.691G>A
AA Mutation	p.Val231Ile(p.V231I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262262
Start	51235224:51235224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757339393
CDS Mutation	c.813C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262262
Start	51225124:51225124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs3959248
CDS Mutation	c.6G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CD33

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262262
Start	51226004:51226004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620G>A
AA Mutation	p.Gly207Asp(p.G207D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262262
Start	51225355:51225355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175T>G
AA Mutation	p.Tyr59Asp(p.Y59D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript