Primary Site >> Stomach Cancer

Gene >> MAPK8IP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000329492
Start 50605714:50605714(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1994G>A
AA Mutation p.Gly665Asp(p.G665D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000329492
Start 50604965:50604965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1666G>A
AA Mutation p.Gly556Ser(p.G556S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000329492
Start 50601887:50601887(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.164G>A
AA Mutation p.Cys55Tyr(p.C55Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000329492
Start 50610711:50610711(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2407G>A
AA Mutation p.Ala803Thr(p.A803T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000329492
Start 50605682:50605682(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1962G>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000329492
Start 50605003:50605003(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1704T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000329492
Start 50605667:50605667(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1951delG
AA Mutation p.Glu651SerfsTer65(p.E651Sfs*65)
Mutation Classification Frame_Shift_Del
Feature Type Transcript