Primary Site >> Stomach Cancer

Gene >> GLG1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000422840
Start 74462131:74462131(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2999G>A
AA Mutation p.Arg1000His(p.R1000H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000422840
Start 74462568:74462568(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761056314
CDS Mutation c.2854G>A
AA Mutation p.Gly952Ser(p.G952S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000422840
Start 74492999:74492999(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1192C>T
AA Mutation p.Leu398Phe(p.L398F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000422840
Start 74492983:74492983(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762159317
CDS Mutation c.1208T>C
AA Mutation p.Met403Thr(p.M403T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000422840
Start 74483033:74483033(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1663C>T
AA Mutation p.Arg555Trp(p.R555W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000422840
Start 74470040:74470040(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2263T>C
AA Mutation p.Phe755Leu(p.F755L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000422840
Start 74491080:74491080(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745573951
CDS Mutation c.1370G>A
AA Mutation p.Arg457Gln(p.R457Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000422840
Start 74606749:74606749(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.346G>A
AA Mutation p.Glu116Lys(p.E116K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000422840
Start 74496609:74496609(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.810G>T
AA Mutation p.Leu270Phe(p.L270F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000422840
Start 74462183:74462183(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2947G>C
AA Mutation p.Asp983His(p.D983H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000422840
Start 74453240:74453240(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3467G>T
AA Mutation p.Cys1156Phe(p.C1156F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000422840
Start 74485865:74485865(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759441082
CDS Mutation c.1502G>A
AA Mutation p.Arg501Gln(p.R501Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000422840
Start 74491194:74491194(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1256G>A
AA Mutation p.Cys419Tyr(p.C419Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000422840
Start 74491111:74491111(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1339delG
AA Mutation p.Glu447ArgfsTer19(p.E447Rfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000422840
Start 74468960:74468960(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2422delG
AA Mutation p.Glu808ArgfsTer5(p.E808Rfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000422840
Start 74485866:74485866(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1501C>T
AA Mutation p.Arg501Ter(p.R501*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000422840
Start 74503683:74503683(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.622C>T
AA Mutation p.Arg208Ter(p.R208*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000422840
Start 74472412:74472412(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2053-1G>T
Mutation Classification Splice_Site
Feature Type Transcript