Primary Site >> Stomach Cancer

Gene >> TPBG

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369750
Start 82365298:82365298(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.337C>T
AA Mutation p.Arg113Cys(p.R113C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369750
Start 82365370:82365370(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.409G>A
AA Mutation p.Ala137Thr(p.A137T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369750
Start 82365938:82365938(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.977C>T
AA Mutation p.Pro326Leu(p.P326L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000369750
Start 82365974:82365974(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1013A>C
AA Mutation p.Asn338Thr(p.N338T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000369750
Start 82366147:82366147(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773064119
CDS Mutation c.1186A>G
AA Mutation p.Met396Val(p.M396V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000369750
Start 82365985:82365985(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1024C>A
AA Mutation p.Leu342Met(p.L342M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000369750
Start 82365175:82365175(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.214G>A
AA Mutation p.Ala72Thr(p.A72T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000369750
Start 82365200:82365200(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.239G>A
AA Mutation p.Arg80His(p.R80H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000369750
Start 82365132:82365132(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.171G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000369750
Start 82365294:82365294(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.333C>T
Mutation Classification Silent
Feature Type Transcript