Primary Site >> Stomach Cancer

Gene >> DSE

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116399654:116399654(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370430595
CDS Mutation c.404C>T
AA Mutation p.Ala135Val(p.A135V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116436761:116436761(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766035826
CDS Mutation c.2293C>T
AA Mutation p.Arg765Trp(p.R765W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116426801:116426801(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs112379267
CDS Mutation c.644C>T
AA Mutation p.Thr215Met(p.T215M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116436930:116436930(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2462C>T
AA Mutation p.Ala821Val(p.A821V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116436582:116436582(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2114G>T
AA Mutation p.Gly705Val(p.G705V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116426689:116426689(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.532C>A
AA Mutation p.Leu178Ile(p.L178I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116436327:116436327(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1859A>G
AA Mutation p.Asp620Gly(p.D620G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116436601:116436601(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2133G>T
AA Mutation p.Gln711His(p.Q711H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000331677
Start 116399658:116399658(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.408G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000331677
Start 116436865:116436865(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2397A>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000331677
Start 116435857:116435857(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1389T>C
Mutation Classification Silent
Feature Type Transcript