Primary Site >> Stomach Cancer

Gene >> BHLHE22

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000321870
Start 64581797:64581797(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1007C>T
AA Mutation p.Pro336Leu(p.P336L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000321870
Start 64581680:64581680(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.890C>T
AA Mutation p.Ala297Val(p.A297V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000321870
Start 64581149:64581149(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.359C>T
AA Mutation p.Pro120Leu(p.P120L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000321870
Start 64581559:64581559(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.769G>A
AA Mutation p.Asp257Asn(p.D257N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000321870
Start 64581869:64581869(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs180818429
CDS Mutation c.1079C>T
AA Mutation p.Pro360Leu(p.P360L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000321870
Start 64581700:64581700(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.910C>T
AA Mutation p.Arg304Trp(p.R304W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000321870
Start 64580862:64580862(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.72C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000321870
Start 64581654:64581654(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.864C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000321870
Start 64581649:64581649(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.859C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000321870
Start 64581189:64581189(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.399G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000321870
Start 64581622:64581622(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.832C>T
AA Mutation p.Arg278Ter(p.R278*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript