Colon Cancer: Gene >> LPAR4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000435339
Start	78754906:78754906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.37G>T
AA Mutation	p.Asp13Tyr(p.D13Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000435339
Start	78755767:78755767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.898G>A
AA Mutation	p.Ala300Thr(p.A300T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000435339
Start	78755267:78755267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.398G>A
AA Mutation	p.Ser133Asn(p.S133N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000435339
Start	78755303:78755303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434G>A
AA Mutation	p.Arg145Gln(p.R145Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000435339
Start	78755752:78755752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883A>T
AA Mutation	p.Ile295Phe(p.I295F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000435339
Start	78755874:78755874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1005G>T
AA Mutation	p.Lys335Asn(p.K335N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000435339
Start	78755555:78755555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686G>A
AA Mutation	p.Arg229Lys(p.R229K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000435339
Start	78755564:78755564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695G>A
AA Mutation	p.Arg232His(p.R232H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000435339
Start	78755148:78755148(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.282delT
AA Mutation	p.Phe94LeufsTer72(p.F94Lfs*72)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000435339
Start	78755602:78755602(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.738delA
AA Mutation	p.Val247TyrfsTer2(p.V247Yfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000435339
Start	78755968:78755968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099G>T
AA Mutation	p.Glu367Ter(p.E367*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000435339
Start	78755409:78755410(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.540_541insACAGGTGA
AA Mutation	p.Val181ThrfsTer40(p.V181Tfs*40)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LPAR4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000435339
Start	78755088:78755088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.219G>T
AA Mutation	p.Glu73Asp(p.E73D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000435339
Start	78755303:78755303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434G>A
AA Mutation	p.Arg145Gln(p.R145Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000435339
Start	78755308:78755308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439C>T
AA Mutation	p.Arg147Cys(p.R147C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript