Primary Site >> Stomach Cancer

Gene >> ILKAP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000254654
Start 238182081:238182081(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.820G>A
AA Mutation p.Ala274Thr(p.A274T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000254654
Start 238170658:238170658(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142248095
CDS Mutation c.1057C>T
AA Mutation p.Arg353Trp(p.R353W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000254654
Start 238182163:238182163(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.738G>T
AA Mutation p.Glu246Asp(p.E246D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000254654
Start 238194293:238194293(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.160G>A
AA Mutation p.Ala54Thr(p.A54T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000254654
Start 238173571:238173571(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.919C>T
AA Mutation p.Pro307Ser(p.P307S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000254654
Start 238173634:238173634(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.856G>A
AA Mutation p.Val286Met(p.V286M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000254654
Start 238194319:238194319(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.134C>A
AA Mutation p.Pro45His(p.P45H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000254654
Start 238184088:238184088(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.558C>T
Mutation Classification Silent
Feature Type Transcript