Colon Cancer: Gene >> SNX27

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000458013
Start	151693429:151693429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1524T>A
AA Mutation	p.Asn508Lys(p.N508K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000458013
Start	151693028:151693028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1507T>A
AA Mutation	p.Phe503Ile(p.F503I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000458013
Start	151638994:151638994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418G>A
AA Mutation	p.Ala140Thr(p.A140T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000458013
Start	151668591:151668591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105C>A
AA Mutation	p.Leu369Ile(p.L369I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000458013
Start	151693038:151693038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1517A>G
AA Mutation	p.Tyr506Cys(p.Y506C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000458013
Start	151639090:151639090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514C>T
AA Mutation	p.His172Tyr(p.H172Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458013
Start	151612264:151612264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.63C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458013
Start	151692985:151692985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767464354
CDS Mutation	c.1464C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458013
Start	151660802:151660802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.741T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000458013
Start	151660797:151660797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.737-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000458013
Start	151693041:151693041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1518+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SNX27

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000458013
Start	151668591:151668591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105C>A
AA Mutation	p.Leu369Ile(p.L369I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript