Primary Site >> Stomach Cancer

Gene >> ISM1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262487
Start 13299299:13299299(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1235C>T
AA Mutation p.Ala412Val(p.A412V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262487
Start 13279865:13279865(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374878260
CDS Mutation c.610C>T
AA Mutation p.Arg204Trp(p.R204W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262487
Start 13299269:13299269(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1205C>T
AA Mutation p.Thr402Met(p.T402M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262487
Start 13279658:13279658(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.403C>A
AA Mutation p.Pro135Thr(p.P135T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262487
Start 13270625:13270625(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768775917
CDS Mutation c.260G>A
AA Mutation p.Arg87Gln(p.R87Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000262487
Start 13299100:13299100(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1036T>G
AA Mutation p.Phe346Val(p.F346V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000262487
Start 13270724:13270724(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.359G>A
AA Mutation p.Gly120Glu(p.G120E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000262487
Start 13292442:13292442(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.856G>A
AA Mutation p.Ala286Thr(p.A286T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000262487
Start 13298960:13298960(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.896G>A
AA Mutation p.Arg299His(p.R299H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000262487
Start 13299126:13299126(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1062C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000262487
Start 13299228:13299228(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1164C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000262487
Start 13279836:13279836(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.585delG
AA Mutation p.Trp196GlyfsTer80(p.W196Gfs*80)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000262487
Start 13279828:13279828(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.579delC
AA Mutation p.Arg194GlyfsTer82(p.R194Gfs*82)
Mutation Classification Frame_Shift_Del
Feature Type Transcript