Colon Cancer: Gene >> LPCAT4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314891
Start	34365158:34365158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.328C>T
AA Mutation	p.Arg110Cys(p.R110C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314891
Start	34365106:34365106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380C>T
AA Mutation	p.Ala127Val(p.A127V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314891
Start	34367051:34367051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.50G>A
AA Mutation	p.Gly17Glu(p.G17E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314891
Start	34364222:34364222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563G>T
AA Mutation	p.Arg188Leu(p.R188L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000314891
Start	34364262:34364262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523C>T
AA Mutation	p.Pro175Ser(p.P175S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000314891
Start	34360205:34360205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1148C>T
AA Mutation	p.Thr383Ile(p.T383I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314891
Start	34367067:34367067(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.34delC
AA Mutation	p.Leu12Ter(p.L12*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000314891
Start	34362299:34362299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907G>T
AA Mutation	p.Glu303Ter(p.E303*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314891
Start	34359232:34359233(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs766365810
CDS Mutation	c.1469dupC
AA Mutation	p.His491ThrfsTer75(p.H491Tfs*75)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000314891
Start	34365229:34365230(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.258-2_258-1insAAGAAAGT
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LPCAT4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314891
Start	34365219:34365219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript