Primary Site >> Stomach Cancer

Gene >> MMP24

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000246186
Start 35274332:35274332(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1661T>C
AA Mutation p.Val554Ala(p.V554A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000246186
Start 35271657:35271657(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1422A>C
AA Mutation p.Glu474Asp(p.E474D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000246186
Start 35274468:35274468(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779868110
CDS Mutation c.1797C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000246186
Start 35263876:35263876(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752992245
CDS Mutation c.903G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000246186
Start 35274381:35274381(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1710C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000246186
Start 35254732:35254732(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs554368304
CDS Mutation c.795G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000246186
Start 35254603:35254604(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.672dupT
AA Mutation p.Ala225CysfsTer12(p.A225Cfs*12)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript