Primary Site >> Stomach Cancer

Gene >> SHOX2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000441443
Start 158102694:158102694(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.539C>T
AA Mutation p.Ser180Leu(p.S180L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000441443
Start 158098208:158098208(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.815C>T
AA Mutation p.Ala272Val(p.A272V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000441443
Start 158102880:158102880(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763913879
CDS Mutation c.353C>T
AA Mutation p.Pro118Leu(p.P118L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000441443
Start 158100266:158100266(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.601C>G
AA Mutation p.Gln201Glu(p.Q201E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000441443
Start 158098111:158098111(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.912A>G
Mutation Classification Silent
Feature Type Transcript