Colon Cancer: Gene >> LPAR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407877
Start	19627043:19627043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.242C>T
AA Mutation	p.Ala81Val(p.A81V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000407877
Start	19627161:19627161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575876718
CDS Mutation	c.124G>A
AA Mutation	p.Val42Ile(p.V42I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000407877
Start	19624300:19624300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012A>G
AA Mutation	p.Met338Val(p.M338V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000407877
Start	19626599:19626599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686A>G
AA Mutation	p.His229Arg(p.H229R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407877
Start	19624292:19624292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1020C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407877
Start	19627039:19627039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407877
Start	19624400:19624400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760187590
CDS Mutation	c.912C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407877
Start	19627042:19627042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759419632
CDS Mutation	c.243G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407877
Start	19626964:19626964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000407877
Start	19626633:19626633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652C>T
AA Mutation	p.Arg218Ter(p.R218*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LPAR2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407877
Start	19624376:19624376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144833106
CDS Mutation	c.936C>T
Mutation Classification	Silent
Feature Type	Transcript