Primary Site >> Stomach Cancer

Gene >> MARVELD3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000268485
Start 71634304:71634304(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.707A>G
AA Mutation p.Tyr236Cys(p.Y236C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000268485
Start 71634538:71634538(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.941C>A
AA Mutation p.Ala314Glu(p.A314E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000268485
Start 71629477:71629477(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.578A>G
AA Mutation p.Tyr193Cys(p.Y193C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000268485
Start 71634402:71634402(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.805A>G
AA Mutation p.Met269Val(p.M269V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000268485
Start 71634299:71634299(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.702C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000268485
Start 71634293:71634293(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.701delG
AA Mutation p.Gly234AlafsTer32(p.G234Afs*32)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000268485
Start 71634266:71634267(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.669_670insT
AA Mutation p.Gly224TrpfsTer25(p.G224Wfs*25)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript