Colon Cancer: Gene >> OPRL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336866
Start	64098644:64098644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779141396
CDS Mutation	c.958G>A
AA Mutation	p.Ala320Thr(p.A320T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336866
Start	64098495:64098495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809C>T
AA Mutation	p.Ala270Val(p.A270V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336866
Start	64098494:64098494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808G>A
AA Mutation	p.Ala270Thr(p.A270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336866
Start	64098452:64098452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376128527
CDS Mutation	c.766C>T
AA Mutation	p.Arg256Trp(p.R256W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336866
Start	64097956:64097956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388G>T
AA Mutation	p.Asp130Tyr(p.D130Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336866
Start	64098011:64098011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768146093
CDS Mutation	c.443G>A
AA Mutation	p.Arg148His(p.R148H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336866
Start	64097821:64097821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253G>A
AA Mutation	p.Ala85Thr(p.A85T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336866
Start	64098712:64098712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145840163
CDS Mutation	c.1026C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336866
Start	64098057:64098057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141501506
CDS Mutation	c.489G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OPRL1

No Mutation Annotation!