Colon Cancer: Gene >> KPNA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330459
Start	68037199:68037199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183061920
CDS Mutation	c.67G>A
AA Mutation	p.Asp23Asn(p.D23N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330459
Start	68043112:68043112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782396125
CDS Mutation	c.679C>T
AA Mutation	p.Arg227Cys(p.R227C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330459
Start	68042110:68042110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.328C>T
AA Mutation	p.Pro110Ser(p.P110S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330459
Start	68043854:68043854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947C>T
AA Mutation	p.Ala316Val(p.A316V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330459
Start	68043168:68043168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782575040
CDS Mutation	c.735G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KPNA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330459
Start	68044048:68044048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1141T>G
AA Mutation	p.Phe381Val(p.F381V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330459
Start	68044497:68044497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1341C>T
Mutation Classification	Silent
Feature Type	Transcript