Colon Cancer: Gene >> PLIN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221957
Start	4852166:4852166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484G>A
AA Mutation	p.Val162Met(p.V162M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221957
Start	4839253:4839253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749599909
CDS Mutation	c.1244C>T
AA Mutation	p.Thr415Met(p.T415M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221957
Start	4847854:4847854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142986276
CDS Mutation	c.671C>T
AA Mutation	p.Ala224Val(p.A224V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221957
Start	4859941:4859941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150G>T
AA Mutation	p.Lys50Asn(p.K50N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221957
Start	4844696:4844696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574992524
CDS Mutation	c.932G>A
AA Mutation	p.Gly311Asp(p.G311D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000221957
Start	4839200:4839200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768566079
CDS Mutation	c.1297A>G
AA Mutation	p.Lys433Glu(p.K433E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221957
Start	4852083:4852083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774125815
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221957
Start	4859911:4859911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PLIN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221957
Start	4839216:4839216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1281G>T
AA Mutation	p.Glu427Asp(p.E427D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript