Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PLA2G5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375108
Start	20084865:20084865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.35C>T
AA Mutation	p.Ala12Val(p.A12V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375108
Start	20086174:20086174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.132C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375108
Start	20084866:20084866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.36T>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PLA2G5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375108
Start	20089883:20089883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>A
AA Mutation	p.Val94Met(p.V94M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375108
Start	20090640:20090640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365T>C
AA Mutation	p.Leu122Pro(p.L122P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript