Colon Cancer: Gene >> PLBD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280800
Start	113380759:113380759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874G>A
AA Mutation	p.Val292Ile(p.V292I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280800
Start	113374878:113374878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761114976
CDS Mutation	c.730T>C
AA Mutation	p.Cys244Arg(p.C244R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280800
Start	113369180:113369180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765071928
CDS Mutation	c.355G>A
AA Mutation	p.Gly119Ser(p.G119S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000280800
Start	113374998:113374998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850G>A
AA Mutation	p.Gly284Ser(p.G284S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PLBD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280800
Start	113387827:113387827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745951952
CDS Mutation	c.1523G>A
AA Mutation	p.Arg508His(p.R508H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280800
Start	113384134:113384134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987G>T
AA Mutation	p.Lys329Asn(p.K329N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript