Colon Cancer: Gene >> OLFM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264833
Start	9854515:9854515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765662180
CDS Mutation	c.1036G>A
AA Mutation	p.Val346Met(p.V346M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264833
Start	9860769:9860769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.89G>A
AA Mutation	p.Gly30Asp(p.G30D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264833
Start	9854832:9854832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554951359
CDS Mutation	c.719G>A
AA Mutation	p.Arg240His(p.R240H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264833
Start	9854744:9854744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764075369
CDS Mutation	c.807G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264833
Start	9854351:9854351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1200G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264833
Start	9854342:9854342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549029152
CDS Mutation	c.1209C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264833
Start	9854702:9854702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.849C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OLFM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264833
Start	9857791:9857791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.284G>A
AA Mutation	p.Gly95Asp(p.G95D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264833
Start	9854407:9854407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148943256
CDS Mutation	c.1144G>A
AA Mutation	p.Val382Met(p.V382M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript