Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SUCNR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000362032
Start	151881432:151881432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.889C>A
AA Mutation	p.Leu297Ile(p.L297I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000362032
Start	151881084:151881084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.541C>T
AA Mutation	p.Pro181Ser(p.P181S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000362032
Start	151880948:151880948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.405G>T
AA Mutation	p.Lys135Asn(p.K135N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000362032
Start	151881018:151881018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475C>T
AA Mutation	p.Pro159Ser(p.P159S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SUCNR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000362032
Start	151881188:151881188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645G>T
AA Mutation	p.Lys215Asn(p.K215N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000362032
Start	151881335:151881335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.792G>T
AA Mutation	p.Lys264Asn(p.K264N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000362032
Start	151881266:151881266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723C>A
AA Mutation	p.Phe241Leu(p.F241L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362032
Start	151881188:151881188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.645G>A
Mutation Classification	Silent
Feature Type	Transcript