Colon Cancer: Gene >> LPCAT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262134
Start	55528562:55528562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762221312
CDS Mutation	c.497G>A
AA Mutation	p.Arg166Gln(p.R166Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262134
Start	55583034:55583034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781024961
CDS Mutation	c.1571C>T
AA Mutation	p.Thr524Ile(p.T524I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262134
Start	55579118:55579118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539874304
CDS Mutation	c.1324G>A
AA Mutation	p.Val442Ile(p.V442I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262134
Start	55545793:55545793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.911A>C
AA Mutation	p.Asn304Thr(p.N304T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262134
Start	55549396:55549396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1055A>C
AA Mutation	p.Lys352Thr(p.K352T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262134
Start	55582921:55582921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1458T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262134
Start	55551039:55551039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550820236
CDS Mutation	c.1152C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000262134
Start	55579148:55579148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1354G>T
AA Mutation	p.Glu452Ter(p.E452*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LPCAT2

No Mutation Annotation!