Primary Site >> Stomach Cancer

Gene >> KIFC1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000428849
Start 33404002:33404002(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773177817
CDS Mutation c.629G>A
AA Mutation p.Arg210His(p.R210H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000428849
Start 33403779:33403779(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.406G>T
AA Mutation p.Ala136Ser(p.A136S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000428849
Start 33406268:33406268(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779218729
CDS Mutation c.1609C>T
AA Mutation p.Arg537Cys(p.R537C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000428849
Start 33406221:33406221(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1562G>T
AA Mutation p.Arg521Leu(p.R521L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000428849
Start 33404994:33404994(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.899T>G
AA Mutation p.Leu300Arg(p.L300R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000428849
Start 33405580:33405580(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1485G>T
AA Mutation p.Glu495Asp(p.E495D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000428849
Start 33398345:33398345(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.208C>G
AA Mutation p.Pro70Ala(p.P70A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000428849
Start 33398151:33398151(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.135C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000428849
Start 33405289:33405289(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1194C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000428849
Start 33406264:33406264(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1605A>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000428849
Start 33406335:33406335(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1681delC
AA Mutation p.Leu561SerfsTer16(p.L561Sfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript