Primary Site >> Stomach Cancer

Gene >> LIN28A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000254231
Start 26411536:26411536(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.182G>A
AA Mutation p.Arg61His(p.R61H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000254231
Start 26411503:26411503(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.149G>A
AA Mutation p.Arg50His(p.R50H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000254231
Start 26426332:26426332(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.504C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000254231
Start 26425404:26425404(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372279965
CDS Mutation c.330C>T
Mutation Classification Silent
Feature Type Transcript