Colon Cancer: Gene >> OPRM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330432
Start	154091287:154091287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.979G>C
AA Mutation	p.Gly327Arg(p.G327R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330432
Start	154091348:154091348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77013544
CDS Mutation	c.1040G>A
AA Mutation	p.Arg347Gln(p.R347Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330432
Start	154039704:154039704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779965433
CDS Mutation	c.160G>A
AA Mutation	p.Gly54Arg(p.G54R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330432
Start	154091282:154091282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974C>T
AA Mutation	p.Ala325Val(p.A325V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330432
Start	154091383:154091383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1075A>G
AA Mutation	p.Asn359Asp(p.N359D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000330432
Start	154091413:154091413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105C>T
AA Mutation	p.Arg369Cys(p.R369C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000330432
Start	154091087:154091087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1799974
CDS Mutation	c.779G>A
AA Mutation	p.Arg260His(p.R260H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330432
Start	154091211:154091211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200986335
CDS Mutation	c.903C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330432
Start	154039787:154039787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200915701
CDS Mutation	c.243C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330432
Start	154090129:154090129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.594A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330432
Start	154039679:154039679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199980523
CDS Mutation	c.135C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330432
Start	154091061:154091061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762355741
CDS Mutation	c.753C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000330432
Start	154091268:154091268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.960G>A
AA Mutation	p.Trp320Ter(p.W320*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000330432
Start	154039637:154039637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.93G>A
AA Mutation	p.Trp31Ter(p.W31*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000330432
Start	154091140:154091140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832C>T
AA Mutation	p.Arg278Ter(p.R278*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> OPRM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330432
Start	154091083:154091083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775T>G
AA Mutation	p.Leu259Val(p.L259V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330432
Start	154091343:154091343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1035C>A
AA Mutation	p.Phe345Leu(p.F345L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000330432
Start	154091140:154091140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832C>T
AA Mutation	p.Arg278Ter(p.R278*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript