Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> OR51B4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380224
Start	5301849:5301849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.98A>G
AA Mutation	p.Tyr33Cys(p.Y33C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380224
Start	5301927:5301927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.20C>T
AA Mutation	p.Ala7Val(p.A7V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380224
Start	5301126:5301126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.821G>C
AA Mutation	p.Ser274Thr(p.S274T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380224
Start	5301739:5301739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372411119
CDS Mutation	c.208G>A
AA Mutation	p.Gly70Arg(p.G70R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380224
Start	5301633:5301633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747263622
CDS Mutation	c.314C>T
AA Mutation	p.Ala105Val(p.A105V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380224
Start	5301451:5301451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496T>C
AA Mutation	p.Cys166Arg(p.C166R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380224
Start	5301719:5301719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.228G>A
AA Mutation	p.Met76Ile(p.M76I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380224
Start	5301581:5301581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OR51B4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380224
Start	5301577:5301577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142325891
CDS Mutation	c.370C>T
AA Mutation	p.Arg124Cys(p.R124C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380224
Start	5301676:5301676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271G>T
AA Mutation	p.Ala91Ser(p.A91S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380224
Start	5301071:5301071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.876G>C
AA Mutation	p.Lys292Asn(p.K292N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380224
Start	5301270:5301270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116026654
CDS Mutation	c.677C>T
AA Mutation	p.Ala226Val(p.A226V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380224
Start	5301647:5301647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300C>A
AA Mutation	p.Phe100Leu(p.F100L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380224
Start	5301230:5301230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375187554
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript