Colon Cancer: Gene >> LPAR5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329858
Start	6621137:6621137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112C>T
AA Mutation	p.Pro38Ser(p.P38S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329858
Start	6621017:6621017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232C>T
AA Mutation	p.Arg78Cys(p.R78C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329858
Start	6620747:6620747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.502C>T
AA Mutation	p.Arg168Trp(p.R168W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329858
Start	6621104:6621104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145C>T
AA Mutation	p.Arg49Cys(p.R49C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329858
Start	6621146:6621146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.103G>T
AA Mutation	p.Ala35Ser(p.A35S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329858
Start	6620508:6620508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550346191
CDS Mutation	c.741C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329858
Start	6620754:6620754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329858
Start	6621152:6621152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.97C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329858
Start	6620886:6620886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LPAR5

No Mutation Annotation!