Colon Cancer: Gene >> PCSK9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302118
Start	55056133:55056133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.940G>A
AA Mutation	p.Ala314Thr(p.A314T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302118
Start	55059588:55059588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776367625
CDS Mutation	c.1606G>A
AA Mutation	p.Val536Ile(p.V536I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302118
Start	55052729:55052729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.737G>T
AA Mutation	p.Ser246Ile(p.S246I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302118
Start	55043925:55043925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376385276
CDS Mutation	c.290G>A
AA Mutation	p.Arg97His(p.R97H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302118
Start	55052771:55052771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777111934
CDS Mutation	c.779C>T
AA Mutation	p.Thr260Met(p.T260M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302118
Start	55058057:55058057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202C>A
AA Mutation	p.Ser401Tyr(p.S401Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302118
Start	55046627:55046627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776208295
CDS Mutation	c.504G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302118
Start	55052396:55052396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302118
Start	55056153:55056153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.960C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PCSK9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302118
Start	55056008:55056008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.815G>T
AA Mutation	p.Arg272Leu(p.R272L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302118
Start	55043887:55043887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768895535
CDS Mutation	c.252G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302118
Start	55057381:55057381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1047G>A
Mutation Classification	Silent
Feature Type	Transcript