Primary Site >> Stomach Cancer

Gene >> MLST8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000397124
Start 2208807:2208807(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.911T>A
AA Mutation p.Ile304Asn(p.I304N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000397124
Start 2207252:2207252(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.480C>A
AA Mutation p.Asp160Glu(p.D160E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000397124
Start 2206518:2206518(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.203A>G
AA Mutation p.Tyr68Cys(p.Y68C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000397124
Start 2208303:2208303(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773318959
CDS Mutation c.667G>A
AA Mutation p.Ala223Thr(p.A223T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000397124
Start 2207279:2207279(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751240038
CDS Mutation c.507C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000397124
Start 2208498:2208498(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.747G>A
Mutation Classification Silent
Feature Type Transcript