Primary Site >> Stomach Cancer

Gene >> ESRRG

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000408911
Start 216564276:216564276(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.805T>A
AA Mutation p.Cys269Ser(p.C269S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000408911
Start 216506946:216506946(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1370A>G
AA Mutation p.Lys457Arg(p.K457R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000408911
Start 216677147:216677147(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.401T>C
AA Mutation p.Ile134Thr(p.I134T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000408911
Start 216519293:216519293(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.991A>T
AA Mutation p.Ile331Leu(p.I331L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000408911
Start 216507081:216507081(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1235G>A
AA Mutation p.Arg412His(p.R412H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000408911
Start 216723287:216723287(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.13G>A
AA Mutation p.Glu5Lys(p.E5K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000408911
Start 216568093:216568093(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.595C>A
AA Mutation p.Arg199Ser(p.R199S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000408911
Start 216677312:216677312(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.236T>G
AA Mutation p.Leu79Arg(p.L79R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000408911
Start 216677186:216677186(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.362A>C
AA Mutation p.Asn121Thr(p.N121T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000408911
Start 216519359:216519359(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.925T>G
AA Mutation p.Leu309Val(p.L309V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000408911
Start 216677232:216677232(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.316A>G
AA Mutation p.Ser106Gly(p.S106G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000408911
Start 216677300:216677300(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.248C>T
AA Mutation p.Pro83Leu(p.P83L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000408911
Start 216507121:216507121(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745321895
CDS Mutation c.1195C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000408911
Start 216519411:216519411(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.873G>A
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000408911
Start 216506964:216506964(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1352delT
AA Mutation p.Leu451TrpfsTer10(p.L451Wfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000408911
Start 216677316:216677316(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.232G>T
AA Mutation p.Gly78Ter(p.G78*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000408911
Start 216506963:216506964(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1352dupT
AA Mutation p.Leu451PhefsTer38(p.L451Ffs*38)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 18
Mutation Consequence inframe_deletion
Transcription ID ENST00000408911
Start 216519294:216519296(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.988_990delTAT
AA Mutation p.Tyr330del(p.Y330del)
Mutation Classification In_Frame_Del
Feature Type Transcript