Colon Cancer: Gene >> PLIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300055
Start	89671507:89671507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754105186
CDS Mutation	c.308C>T
AA Mutation	p.Pro103Leu(p.P103L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300055
Start	89667159:89667159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372063597
CDS Mutation	c.986G>A
AA Mutation	p.Arg329Gln(p.R329Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300055
Start	89671505:89671505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756661343
CDS Mutation	c.310G>A
AA Mutation	p.Ala104Thr(p.A104T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300055
Start	89671489:89671489(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.326delC
AA Mutation	p.Pro109LeufsTer8(p.P109Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PLIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300055
Start	89667122:89667122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1023G>T
AA Mutation	p.Lys341Asn(p.K341N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300055
Start	89677486:89677486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4G>A
AA Mutation	p.Ala2Thr(p.A2T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript