Primary Site >> Stomach Cancer

Gene >> SIX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000247182
Start 60648877:60648877(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.313G>A
AA Mutation p.Ala105Thr(p.A105T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000247182
Start 60646294:60646294(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.844T>G
AA Mutation p.Leu282Val(p.L282V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000247182
Start 60649103:60649103(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.87C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000247182
Start 60648758:60648758(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.432G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence inframe_insertion
Transcription ID ENST00000247182
Start 60648938:60648939(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.219_251dupCCAGTTCTCGCCTCACAACCACCCCAAACTGCA
AA Mutation p.His73_Leu83dup(p.H73_L83dup)
Mutation Classification In_Frame_Ins
Feature Type Transcript