Primary Site >> Stomach Cancer

Gene >> PDHB

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302746
Start 58428587:58428587(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.820A>G
AA Mutation p.Met274Val(p.M274V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302746
Start 58431609:58431609(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.287C>T
AA Mutation p.Ala96Val(p.A96V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302746
Start 58428140:58428140(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.974T>C
AA Mutation p.Val325Ala(p.V325A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000302746
Start 58428108:58428108(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767192593
CDS Mutation c.1006A>G
AA Mutation p.Lys336Glu(p.K336E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000302746
Start 58431979:58431979(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.102A>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000302746
Start 58433676:58433676(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.51G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000302746
Start 58430733:58430733(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.513C>T
Mutation Classification Silent
Feature Type Transcript