Primary Site >> Stomach Cancer

Gene >> DPYSL2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000311151
Start 26643528:26643528(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.901T>G
AA Mutation p.Phe301Val(p.F301V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000311151
Start 26647717:26647717(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765277758
CDS Mutation c.1198C>T
AA Mutation p.Arg400Cys(p.R400C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000311151
Start 26583894:26583894(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759388658
CDS Mutation c.224G>A
AA Mutation p.Arg75His(p.R75H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000311151
Start 26634859:26634859(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.770G>A
AA Mutation p.Ser257Asn(p.S257N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000311151
Start 26624151:26624151(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752044385
CDS Mutation c.322G>A
AA Mutation p.Val108Ile(p.V108I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000311151
Start 26624243:26624243(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.414T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000311151
Start 26647731:26647731(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1212A>T
Mutation Classification Silent
Feature Type Transcript