Primary Site >> Stomach Cancer

Gene >> MAGT1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000618282
Start 77857412:77857412(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782169515
CDS Mutation c.476G>A
AA Mutation p.Arg159Gln(p.R159Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000618282
Start 77895386:77895386(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.25T>C
AA Mutation p.Cys9Arg(p.C9R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000618282
Start 77895371:77895371(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782145425
CDS Mutation c.40A>G
AA Mutation p.Met14Val(p.M14V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000618282
Start 77856840:77856840(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781861140
CDS Mutation c.565C>T
AA Mutation p.Pro189Ser(p.P189S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000618282
Start 77875516:77875516(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.184C>T
AA Mutation p.Arg62Cys(p.R62C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000618282
Start 77857479:77857479(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.409C>T
AA Mutation p.Pro137Ser(p.P137S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000618282
Start 77855581:77855581(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.682C>T
AA Mutation p.Leu228Phe(p.L228F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000618282
Start 77841256:77841256(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.891A>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000618282
Start 77855521:77855542(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.721_742delGGACCACCATATGCCCATAAGA
AA Mutation p.Gly241IlefsTer7(p.G241Ifs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript