Primary Site >> Stomach Cancer

Gene >> MAP4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47872017:47872017(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2406G>T
AA Mutation p.Lys802Asn(p.K802N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47916595:47916595(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1232T>C
AA Mutation p.Val411Ala(p.V411A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47916665:47916665(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1162A>G
AA Mutation p.Met388Val(p.M388V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47921824:47921824(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200887208
CDS Mutation c.470G>A
AA Mutation p.Ser157Asn(p.S157N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47869290:47869290(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771820978
CDS Mutation c.2897C>T
AA Mutation p.Thr966Ile(p.T966I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47916462:47916462(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1365A>C
AA Mutation p.Glu455Asp(p.E455D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000360240
Start 47872062:47872062(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2361A>G
Mutation Classification Silent
Feature Type Transcript