Primary Site >> Stomach Cancer

Gene >> KLKB1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264690
Start 186236857:186236857(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.405A>C
AA Mutation p.Glu135Asp(p.E135D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264690
Start 186256002:186256002(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760562034
CDS Mutation c.1500A>C
AA Mutation p.Lys500Asn(p.K500N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264690
Start 186233987:186233987(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.257C>T
AA Mutation p.Thr86Ile(p.T86I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264690
Start 186233981:186233981(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.251C>T
AA Mutation p.Thr84Ile(p.T84I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264690
Start 186251799:186251799(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747716379
CDS Mutation c.1082C>T
AA Mutation p.Ala361Val(p.A361V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264690
Start 186251854:186251854(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1137C>A
AA Mutation p.Asp379Glu(p.D379E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000264690
Start 186251800:186251800(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs567160749
CDS Mutation c.1083G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000264690
Start 186252114:186252114(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1242T>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000264690
Start 186254692:186254692(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1421delA
AA Mutation p.Asn474ThrfsTer13(p.N474Tfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000264690
Start 186257350:186257350(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1713delA
AA Mutation p.Asp572MetfsTer11(p.D572Mfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript