Colon Cancer: Gene >> NUP88

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5387091:5387091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1936A>C
AA Mutation	p.Ser646Arg(p.S646R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5387873:5387873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1675G>A
AA Mutation	p.Glu559Lys(p.E559K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5391589:5391589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1456A>G
AA Mutation	p.Thr486Ala(p.T486A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5419553:5419553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.98A>G
AA Mutation	p.Asn33Ser(p.N33S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5408850:5408850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740C>T
AA Mutation	p.Ala247Val(p.A247V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5419500:5419500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151C>T
AA Mutation	p.Pro51Ser(p.P51S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000573584
Start	5419516:5419516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000573584
Start	5416662:5416662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.318A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000573584
Start	5419501:5419501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000573584
Start	5419415:5419415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.236T>A
AA Mutation	p.Leu79Ter(p.L79*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NUP88

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5394971:5394971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1302T>G
AA Mutation	p.Asp434Glu(p.D434E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5399561:5399561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282C>A
AA Mutation	p.Leu428Ile(p.L428I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript