Colon Cancer: Gene >> SMPD2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000258052
Start	109442884:109442884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.624G>T
AA Mutation	p.Lys208Asn(p.K208N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258052
Start	109443735:109443735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102G>T
AA Mutation	p.Ala368Ser(p.A368S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258052
Start	109443027:109443027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.675G>C
AA Mutation	p.Gln225His(p.Q225H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000258052
Start	109441359:109441359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138354272
CDS Mutation	c.53G>A
AA Mutation	p.Gly18Asp(p.G18D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258052
Start	109443522:109443522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.889G>A
AA Mutation	p.Ala297Thr(p.A297T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258052
Start	109442552:109442552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150792146
CDS Mutation	c.418G>A
AA Mutation	p.Glu140Lys(p.E140K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000258052
Start	109443064:109443064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712G>T
AA Mutation	p.Asp238Tyr(p.D238Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000258052
Start	109443070:109443070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142939267
CDS Mutation	c.718G>A
AA Mutation	p.Val240Met(p.V240M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258052
Start	109442284:109442284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371903352
CDS Mutation	c.393C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SMPD2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258052
Start	109442773:109442773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201190627
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript