Colon Cancer: Gene >> LPCAT1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000283415
Start	1483429:1483429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.725T>G
AA Mutation	p.Leu242Arg(p.L242R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283415
Start	1501600:1501600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139G>A
AA Mutation	p.Ala47Thr(p.A47T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000283415
Start	1489748:1489748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.604C>G
AA Mutation	p.Gln202Glu(p.Q202E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000283415
Start	1463747:1463747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1509G>T
AA Mutation	p.Glu503Asp(p.E503D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000283415
Start	1494835:1494835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747860604
CDS Mutation	c.358C>T
AA Mutation	p.Arg120Trp(p.R120W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000283415
Start	1488403:1488403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655A>G
AA Mutation	p.Thr219Ala(p.T219A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000283415
Start	1489774:1489774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780038428
CDS Mutation	c.578G>A
AA Mutation	p.Arg193Gln(p.R193Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000283415
Start	1479628:1479628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.809A>T
AA Mutation	p.Glu270Val(p.E270V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283415
Start	1466861:1466861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774319281
CDS Mutation	c.1308C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283415
Start	1494827:1494827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283415
Start	1474652:1474652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769756864
CDS Mutation	c.933C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283415
Start	1466879:1466879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763872166
CDS Mutation	c.1290G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000283415
Start	1474559:1474559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1025+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LPCAT1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283415
Start	1463723:1463723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748548369
CDS Mutation	c.1533C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283415
Start	1463762:1463762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758011089
CDS Mutation	c.1494C>T
Mutation Classification	Silent
Feature Type	Transcript