Colon Cancer: Gene >> SENP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000448372
Start	48048983:48048983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1557T>G
AA Mutation	p.Phe519Leu(p.F519L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000448372
Start	48096396:48096396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.167G>A
AA Mutation	p.Arg56Gln(p.R56Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000448372
Start	48065072:48065072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1268T>A
AA Mutation	p.Ile423Asn(p.I423N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000448372
Start	48074537:48074537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727T>G
AA Mutation	p.Ser243Ala(p.S243A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000448372
Start	48065643:48065643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539740517
CDS Mutation	c.1072C>T
AA Mutation	p.Arg358Cys(p.R358C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000448372
Start	48065089:48065089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1251A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000448372
Start	48098009:48098009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751030434
CDS Mutation	c.120G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SENP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000448372
Start	48074374:48074374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890C>A
AA Mutation	p.Ser297Tyr(p.S297Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000448372
Start	48063810:48063810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771938522
CDS Mutation	c.1307G>A
AA Mutation	p.Arg436His(p.R436H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000448372
Start	48065644:48065644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1071G>A
Mutation Classification	Silent
Feature Type	Transcript