Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KPNA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261667
Start	49719791:49719791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755A>G
AA Mutation	p.Tyr252Cys(p.Y252C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261667
Start	49705669:49705669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1324G>A
AA Mutation	p.Ala442Thr(p.A442T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261667
Start	49705667:49705667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535292951
CDS Mutation	c.1326C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261667
Start	49705683:49705683(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1310delA
AA Mutation	p.Asn437ThrfsTer3(p.N437Tfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000261667
Start	49706148:49706148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1159G>T
AA Mutation	p.Glu387Ter(p.E387*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KPNA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261667
Start	49733015:49733015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146G>C
AA Mutation	p.Arg49Thr(p.R49T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261667
Start	49701841:49701841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1525G>C
AA Mutation	p.Asp509His(p.D509H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261667
Start	49709578:49709578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1026A>G
AA Mutation	p.Ile342Met(p.I342M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript