Primary Site >> Stomach Cancer

Gene >> MLNR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000218721
Start 49221010:49221010(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374254248
CDS Mutation c.673G>A
AA Mutation p.Ala225Thr(p.A225T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000218721
Start 49220711:49220711(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.374C>T
AA Mutation p.Thr125Met(p.T125M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000218721
Start 49222232:49222232(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1094C>T
AA Mutation p.Ala365Val(p.A365V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000218721
Start 49221200:49221200(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.863G>A
AA Mutation p.Gly288Glu(p.G288E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000218721
Start 49221138:49221138(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.801C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000218721
Start 49220871:49220871(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.534C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000218721
Start 49220484:49220484(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.147C>T
Mutation Classification Silent
Feature Type Transcript