Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ADIPOQ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320741
Start	186854630:186854630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138773406
CDS Mutation	c.661C>T
AA Mutation	p.Arg221Cys(p.R221C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320741
Start	186854424:186854424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.455G>A
AA Mutation	p.Cys152Tyr(p.C152Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320741
Start	186853219:186853219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161G>A
AA Mutation	p.Gly54Asp(p.G54D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320741
Start	186854396:186854396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427T>G
AA Mutation	p.Tyr143Asp(p.Y143D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000320741
Start	186854262:186854262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.293A>G
AA Mutation	p.Gln98Arg(p.Q98R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320741
Start	186854692:186854692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.723T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ADIPOQ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320741
Start	186854661:186854661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.692A>G
AA Mutation	p.Asp231Gly(p.D231G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320741
Start	186853138:186853138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.80T>C
AA Mutation	p.Val27Ala(p.V27A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320741
Start	186853170:186853170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112G>T
AA Mutation	p.Gly38Cys(p.G38C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript