Primary Site >> Stomach Cancer

Gene >> MAGEA3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370278
Start 152701547:152701547(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.715T>G
AA Mutation p.Leu239Val(p.L239V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370278
Start 152701200:152701200(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.368A>G
AA Mutation p.Lys123Arg(p.K123R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370278
Start 152701598:152701598(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.766C>G
AA Mutation p.Leu256Val(p.L256V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370278
Start 152701495:152701495(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.663C>G
AA Mutation p.Ile221Met(p.I221M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000370278
Start 152701218:152701218(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.386C>T
AA Mutation p.Pro129Leu(p.P129L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000370278
Start 152701262:152701262(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.430C>A
AA Mutation p.Gln144Lys(p.Q144K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000370278
Start 152701377:152701377(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.545T>C
AA Mutation p.Leu182Pro(p.L182P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000370278
Start 152701600:152701600(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.768G>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000370278
Start 152701714:152701714(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.882T>C
Mutation Classification Silent
Feature Type Transcript