Colon Cancer: Gene >> OLFM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219022
Start	53050184:53050184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946A>T
AA Mutation	p.Ile316Leu(p.I316L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219022
Start	53041948:53041948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.396G>T
AA Mutation	p.Lys132Asn(p.K132N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219022
Start	53043153:53043153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619A>T
AA Mutation	p.Asn207Tyr(p.N207Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000219022
Start	53028902:53028902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.66G>T
AA Mutation	p.Leu22Phe(p.L22F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000219022
Start	53042021:53042021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370172371
CDS Mutation	c.469G>A
AA Mutation	p.Glu157Lys(p.E157K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000219022
Start	53050440:53050440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202G>A
AA Mutation	p.Ser401Asn(p.S401N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000219022
Start	53050698:53050698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1460A>C
AA Mutation	p.Asp487Ala(p.D487A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000219022
Start	53050584:53050584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346G>A
AA Mutation	p.Arg449Lys(p.R449K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219022
Start	53041933:53041933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.381T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219022
Start	53050111:53050111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147184057
CDS Mutation	c.873G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000219022
Start	53043177:53043177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643G>T
AA Mutation	p.Glu215Ter(p.E215*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000219022
Start	53029042:53029042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> OLFM4

No Mutation Annotation!