Primary Site >> Stomach Cancer

Gene >> KIF2C

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000372224
Start 44760410:44760410(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766564343
CDS Mutation c.1498G>A
AA Mutation p.Ala500Thr(p.A500T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000372224
Start 44753233:44753233(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.541T>G
AA Mutation p.Ser181Ala(p.S181A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000372224
Start 44753243:44753243(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.551C>A
AA Mutation p.Pro184His(p.P184H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000372224
Start 44750544:44750544(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200680875
CDS Mutation c.419G>A
AA Mutation p.Arg140His(p.R140H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000372224
Start 44757923:44757923(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1084C>T
AA Mutation p.Leu362Phe(p.L362F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000372224
Start 44767099:44767099(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2098G>C
AA Mutation p.Val700Leu(p.V700L)
Mutation Classification Missense_Mutation
Feature Type Transcript