Primary Site >> Stomach Cancer

Gene >> KLHL9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359039
Start 21333695:21333695(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1165C>T
AA Mutation p.Arg389Cys(p.R389C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359039
Start 21334481:21334481(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.379G>A
AA Mutation p.Glu127Lys(p.E127K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359039
Start 21333292:21333292(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1568A>G
AA Mutation p.Asp523Gly(p.D523G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359039
Start 21333641:21333641(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1219C>T
AA Mutation p.Arg407Cys(p.R407C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359039
Start 21333895:21333895(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.965A>G
AA Mutation p.Glu322Gly(p.E322G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000359039
Start 21333735:21333735(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1125G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000359039
Start 21334794:21334794(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.66A>G
Mutation Classification Silent
Feature Type Transcript