Primary Site >> Stomach Cancer

Gene >> KPNA2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000330459
Start 68044357:68044357(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782484137
CDS Mutation c.1201G>A
AA Mutation p.Val401Met(p.V401M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000330459
Start 68037481:68037481(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.199A>C
AA Mutation p.Asn67His(p.N67H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000330459
Start 68042287:68042287(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.505T>C
AA Mutation p.Ser169Pro(p.S169P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000330459
Start 68037199:68037199(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs183061920
CDS Mutation c.67G>C
AA Mutation p.Asp23His(p.D23H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000330459
Start 68044484:68044484(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1328C>T
AA Mutation p.Ala443Val(p.A443V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000330459
Start 68037456:68037456(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.174T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000330459
Start 68040746:68040746(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.282C>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000330459
Start 68044032:68044042(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1127_1137delATGGATTAGTC
AA Mutation p.His376ProfsTer9(p.H376Pfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000330459
Start 68043286:68043286(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.853C>T
AA Mutation p.Arg285Ter(p.R285*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript