Primary Site >> Stomach Cancer

Gene >> BHLHE23

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370346
Start 63006321:63006321(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781619083
CDS Mutation c.406C>T
AA Mutation p.Arg136Cys(p.R136C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370346
Start 63006408:63006408(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.319G>A
AA Mutation p.Ala107Thr(p.A107T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370346
Start 63006360:63006360(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.367C>A
AA Mutation p.Leu123Met(p.L123M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370346
Start 63006398:63006398(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.329G>A
AA Mutation p.Arg110Gln(p.R110Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000370346
Start 63006200:63006200(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.527C>T
AA Mutation p.Ala176Val(p.A176V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000370346
Start 63006371:63006371(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.356C>T
AA Mutation p.Ala119Val(p.A119V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000370346
Start 63006376:63006376(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.351C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000370346
Start 63006184:63006184(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.543G>A
Mutation Classification Silent
Feature Type Transcript