Colon Cancer: Gene >> LPAR6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345941
Start	48412149:48412149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275C>T
AA Mutation	p.Ser92Phe(p.S92F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345941
Start	48412189:48412189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.235A>G
AA Mutation	p.Thr79Ala(p.T79A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345941
Start	48411710:48411710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714C>A
AA Mutation	p.Phe238Leu(p.F238L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345941
Start	48411819:48411819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605C>T
AA Mutation	p.Thr202Ile(p.T202I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345941
Start	48412150:48412150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274T>C
AA Mutation	p.Ser92Pro(p.S92P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345941
Start	48411911:48411911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.513T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345941
Start	48411392:48411392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772128045
CDS Mutation	c.1032C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345941
Start	48411835:48411835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.589C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345941
Start	48411764:48411764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345941
Start	48411727:48411728(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.696dupT
AA Mutation	p.Val233CysfsTer30(p.V233Cfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LPAR6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345941
Start	48411423:48411423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1001A>C
AA Mutation	p.Lys334Thr(p.K334T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345941
Start	48411540:48411540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367788266
CDS Mutation	c.884C>T
AA Mutation	p.Ser295Leu(p.S295L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345941
Start	48411455:48411455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.969G>T
AA Mutation	p.Glu323Asp(p.E323D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345941
Start	48412382:48412382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345941
Start	48411618:48411622(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.802_806delGCAGT
AA Mutation	p.Ala268LysfsTer18(p.A268Kfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript