Primary Site >> Stomach Cancer

Gene >> ATOH1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000306011
Start 93829299:93829299(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.373C>T
AA Mutation p.Arg125Trp(p.R125W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000306011
Start 93829269:93829269(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.343A>G
AA Mutation p.Ser115Gly(p.S115G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000306011
Start 93829442:93829442(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.516G>A
AA Mutation p.Met172Ile(p.M172I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000306011
Start 93829028:93829028(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.102G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000306011
Start 93829895:93829895(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371160490
CDS Mutation c.969G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000306011
Start 93829772:93829772(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.846G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000306011
Start 93829231:93829231(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.310delG
AA Mutation p.Glu104SerfsTer3(p.E104Sfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript