Primary Site >> Stomach Cancer

Gene >> MMP11

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000215743
Start 23782379:23782379(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747596627
CDS Mutation c.1229G>A
AA Mutation p.Arg410His(p.R410H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000215743
Start 23780441:23780441(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.421A>C
AA Mutation p.Thr141Pro(p.T141P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000215743
Start 23783494:23783494(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1417G>A
AA Mutation p.Val473Met(p.V473M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000215743
Start 23783429:23783429(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776950374
CDS Mutation c.1352G>A
AA Mutation p.Arg451His(p.R451H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000215743
Start 23780412:23780412(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.392C>T
AA Mutation p.Ala131Val(p.A131V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000215743
Start 23781259:23781259(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.929delT
AA Mutation p.Phe310SerfsTer74(p.F310Sfs*74)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000215743
Start 23782269:23782269(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1122delC
AA Mutation p.Ala375HisfsTer9(p.A375Hfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000215743
Start 23780581:23780581(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.483-1G>T
Mutation Classification Splice_Site
Feature Type Transcript