Primary Site >> Stomach Cancer

Gene >> KIF22

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000160827
Start 29805284:29805284(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1972G>T
AA Mutation p.Ala658Ser(p.A658S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000160827
Start 29798999:29798999(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.574T>A
AA Mutation p.Ser192Thr(p.S192T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000160827
Start 29798426:29798426(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.319T>C
AA Mutation p.Ser107Pro(p.S107P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000160827
Start 29804953:29804953(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1817G>T
AA Mutation p.Ser606Ile(p.S606I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000160827
Start 29799150:29799150(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs550717370
CDS Mutation c.725G>A
AA Mutation p.Arg242His(p.R242H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000160827
Start 29803593:29803593(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1594A>G
AA Mutation p.Met532Val(p.M532V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000160827
Start 29804971:29804971(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1835C>T
AA Mutation p.Pro612Leu(p.P612L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000160827
Start 29804041:29804041(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1653G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000160827
Start 29798600:29798600(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.402G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000160827
Start 29802856:29802856(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1372delG
AA Mutation p.Ala458ProfsTer4(p.A458Pfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript