Colon Cancer: Gene >> BPI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262865
Start	38304228:38304228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.17C>T
AA Mutation	p.Ala6Val(p.A6V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262865
Start	38311918:38311918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749629986
CDS Mutation	c.593G>A
AA Mutation	p.Arg198Gln(p.R198Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262865
Start	38323949:38323949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183269384
CDS Mutation	c.848G>A
AA Mutation	p.Arg283His(p.R283H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262865
Start	38310526:38310526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.422G>A
AA Mutation	p.Gly141Asp(p.G141D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262865
Start	38307674:38307674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250T>A
AA Mutation	p.Phe84Ile(p.F84I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262865
Start	38327610:38327610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1196T>C
AA Mutation	p.Val399Ala(p.V399A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262865
Start	38326320:38326320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555002988
CDS Mutation	c.1061C>T
AA Mutation	p.Pro354Leu(p.P354L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262865
Start	38323908:38323908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.807C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262865
Start	38337160:38337160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145842777
CDS Mutation	c.1440C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262865
Start	38326300:38326300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1041C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262865
Start	38308954:38308954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.282T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262865
Start	38318442:38318442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.642C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BPI

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262865
Start	38331089:38331089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375769120
CDS Mutation	c.1283C>T
AA Mutation	p.Pro428Leu(p.P428L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262865
Start	38310502:38310502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398G>A
AA Mutation	p.Gly133Asp(p.G133D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262865
Start	38304246:38304246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs5743498
CDS Mutation	c.35C>T
AA Mutation	p.Ala12Val(p.A12V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262865
Start	38335599:38335599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142119049
CDS Mutation	c.1350G>T
AA Mutation	p.Glu450Asp(p.E450D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262865
Start	38324032:38324032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931C>A
AA Mutation	p.Leu311Ile(p.L311I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262865
Start	38337160:38337160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145842777
CDS Mutation	c.1440C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262865
Start	38304250:38304250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768049988
CDS Mutation	c.39G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262865
Start	38326306:38326306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1047C>A
Mutation Classification	Silent
Feature Type	Transcript