Primary Site >> Stomach Cancer

Gene >> MASTL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375940
Start 27170106:27170106(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs117134003
CDS Mutation c.1147C>T
AA Mutation p.Arg383Cys(p.R383C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375940
Start 27170604:27170604(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1645T>A
AA Mutation p.Leu549Ile(p.L549I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000375940
Start 27170330:27170330(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1371A>C
AA Mutation p.Lys457Asn(p.K457N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000375940
Start 27170083:27170083(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1124G>A
AA Mutation p.Ser375Asn(p.S375N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000375940
Start 27181496:27181496(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2397A>C
AA Mutation p.Glu799Asp(p.E799D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000375940
Start 27170029:27170029(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367614863
CDS Mutation c.1070C>T
AA Mutation p.Thr357Met(p.T357M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000375940
Start 27165422:27165422(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763897918
CDS Mutation c.694G>A
AA Mutation p.Ala232Thr(p.A232T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000375940
Start 27165483:27165483(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.755C>A
AA Mutation p.Pro252His(p.P252H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000375940
Start 27170801:27170801(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1842C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000375940
Start 27170127:27170127(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1173delA
AA Mutation p.Lys391AsnfsTer12(p.K391Nfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000375940
Start 27170325:27170325(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1372delA
AA Mutation p.Ile458LeufsTer9(p.I458Lfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000375940
Start 27170343:27170343(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1390delA
AA Mutation p.Thr464LeufsTer3(p.T464Lfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript