Primary Site >> Stomach Cancer

Gene >> MAGEA12

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357916
Start 152736786:152736786(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.625A>G
AA Mutation p.Ile209Val(p.I209V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357916
Start 152736905:152736905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.744A>C
AA Mutation p.Gln248His(p.Q248H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000357916
Start 152736876:152736876(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.715T>A
AA Mutation p.Phe239Ile(p.F239I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000357916
Start 152736658:152736658(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.497T>C
AA Mutation p.Val166Ala(p.V166A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000357916
Start 152736950:152736950(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.789C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000357916
Start 152736731:152736731(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.570G>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000357916
Start 152736320:152736320(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.159G>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000357916
Start 152736896:152736896(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.735G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000357916
Start 152736905:152736905(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.744A>G
Mutation Classification Silent
Feature Type Transcript