Colon Cancer: Gene >> PLIN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276914
Start	19123620:19123620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.254A>G
AA Mutation	p.Lys85Arg(p.K85R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276914
Start	19116549:19116549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013A>C
AA Mutation	p.Asn338Thr(p.N338T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276914
Start	19116509:19116509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778848881
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000276914
Start	19116520:19116520(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1042delG
AA Mutation	p.Val348Ter(p.V348*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PLIN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276914
Start	19118438:19118438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373365753
CDS Mutation	c.795G>T
AA Mutation	p.Lys265Asn(p.K265N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276914
Start	19126238:19126238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.102C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000276914
Start	19116469:19116469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093G>T
AA Mutation	p.Glu365Ter(p.E365*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000276914
Start	19126112:19126112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.226+2T>A
Mutation Classification	Splice_Site
Feature Type	Transcript