Primary Site >> Stomach Cancer

Gene >> MYBL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000522677
Start 66576225:66576225(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1252A>G
AA Mutation p.Lys418Glu(p.K418E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000522677
Start 66576028:66576028(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765182430
CDS Mutation c.1449A>G
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000522677
Start 66580310:66580310(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.924T>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000522677
Start 66576218:66576218(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1259delA
AA Mutation p.Asn420ThrfsTer13(p.N420Tfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000522677
Start 66576369:66576369(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1108delG
AA Mutation p.Val370Ter(p.V370*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000522677
Start 66576217:66576218(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1259dupA
AA Mutation p.Asn420LysfsTer4(p.N420Kfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript