Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LPAR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358883
Start	110941598:110941598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616T>C
AA Mutation	p.Tyr206His(p.Y206H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358883
Start	110941873:110941873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778252713
CDS Mutation	c.341G>A
AA Mutation	p.Arg114Gln(p.R114Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358883
Start	110941664:110941664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550G>A
AA Mutation	p.Val184Met(p.V184M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358883
Start	110875575:110875575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769855870
CDS Mutation	c.941G>A
AA Mutation	p.Arg314His(p.R314H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358883
Start	110875715:110875715(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.801delT
AA Mutation	p.Phe267LeufsTer14(p.F267Lfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000358883
Start	110941650:110941650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564T>A
AA Mutation	p.Cys188Ter(p.C188*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LPAR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358883
Start	110941843:110941843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371G>A
AA Mutation	p.Arg124His(p.R124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358883
Start	110875637:110875637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.879G>T
AA Mutation	p.Glu293Asp(p.E293D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358883
Start	110941781:110941781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433G>A
AA Mutation	p.Glu145Lys(p.E145K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358883
Start	110875554:110875554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.962C>T
AA Mutation	p.Thr321Ile(p.T321I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript