Colon Cancer: Gene >> PGAP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300658
Start	39673543:39673543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.665G>A
AA Mutation	p.Gly222Asp(p.G222D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300658
Start	39673064:39673064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369388252
CDS Mutation	c.886G>A
AA Mutation	p.Val296Ile(p.V296I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300658
Start	39684704:39684704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752623171
CDS Mutation	c.325G>A
AA Mutation	p.Val109Met(p.V109M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300658
Start	39673551:39673551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372234504
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300658
Start	39673122:39673122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375997053
CDS Mutation	c.828G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300658
Start	39673568:39673568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300658
Start	39684659:39684659(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.370delC
AA Mutation	p.Arg124AlafsTer84(p.R124Afs*84)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PGAP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300658
Start	39673064:39673064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369388252
CDS Mutation	c.886G>A
AA Mutation	p.Val296Ile(p.V296I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300658
Start	39687855:39687855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160C>T
AA Mutation	p.Pro54Ser(p.P54S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript