Primary Site >> Stomach Cancer

Gene >> NHLH1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302101
Start 160370976:160370976(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.245C>T
AA Mutation p.Thr82Met(p.T82M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302101
Start 160370927:160370927(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.196C>T
AA Mutation p.Arg66Cys(p.R66C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302101
Start 160371042:160371042(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.311C>T
AA Mutation p.Thr104Met(p.T104M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000302101
Start 160370965:160370965(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.234G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000302101
Start 160370794:160370794(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.63G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000302101
Start 160371043:160371043(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.312G>A
Mutation Classification Silent
Feature Type Transcript