Colon Cancer: Gene >> NUP62

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352066
Start	49909233:49909233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139206027
CDS Mutation	c.575C>T
AA Mutation	p.Pro192Leu(p.P192L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352066
Start	49908771:49908771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037A>G
AA Mutation	p.Asp346Gly(p.D346G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000352066
Start	49909140:49909140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.668C>A
AA Mutation	p.Ala223Glu(p.A223E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000352066
Start	49909704:49909704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769926725
CDS Mutation	c.104C>T
AA Mutation	p.Ser35Phe(p.S35F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000352066
Start	49908856:49908856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139269985
CDS Mutation	c.952G>A
AA Mutation	p.Ala318Thr(p.A318T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352066
Start	49909373:49909373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352066
Start	49909748:49909748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60T>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NUP62

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352066
Start	49908443:49908443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1365C>T
Mutation Classification	Silent
Feature Type	Transcript