Colon Cancer: Gene >> PLP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376327
Start	49173139:49173139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107T>C
AA Mutation	p.Leu36Pro(p.L36P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376327
Start	49173162:49173162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130G>A
AA Mutation	p.Ala44Thr(p.A44T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376327
Start	49173244:49173244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782368813
CDS Mutation	c.212T>C
AA Mutation	p.Leu71Pro(p.L71P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376327
Start	49174676:49174676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141287647
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376327
Start	49172060:49172060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PLP2

No Mutation Annotation!