Primary Site >> Stomach Cancer

Gene >> POM121

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000434423
Start 72928465:72928465(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1103A>T
AA Mutation p.Lys368Met(p.K368M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000434423
Start 72942050:72942050(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs551810669
CDS Mutation c.2057C>T
AA Mutation p.Thr686Met(p.T686M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000434423
Start 72942916:72942916(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782328273
CDS Mutation c.2923G>A
AA Mutation p.Ala975Thr(p.A975T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000434423
Start 72942124:72942124(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2131A>G
AA Mutation p.Thr711Ala(p.T711A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000434423
Start 72946167:72946167(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377106663
CDS Mutation c.3683C>T
AA Mutation p.Ala1228Val(p.A1228V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000434423
Start 72942288:72942288(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2295C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000434423
Start 72938607:72938607(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1293C>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000434423
Start 72945698:72945698(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3642T>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000434423
Start 72942885:72942885(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782716752
CDS Mutation c.2892G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000434423
Start 72943095:72943095(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139238552
CDS Mutation c.3102G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000434423
Start 72938642:72938642(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1330delC
AA Mutation p.Arg444AlafsTer12(p.R444Afs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000434423
Start 72930097:72930097(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1261C>T
AA Mutation p.Arg421Ter(p.R421*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000434423
Start 72926888:72926889(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.948dupC
AA Mutation p.Lys317GlnfsTer18(p.K317Qfs*18)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript