Primary Site >> Stomach Cancer

Gene >> SCPEP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262288
Start 56981142:56981142(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs556719579
CDS Mutation c.137G>A
AA Mutation p.Arg46His(p.R46H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262288
Start 57002071:57002071(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1186C>A
AA Mutation p.Gln396Lys(p.Q396K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262288
Start 56987764:56987764(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.385G>C
AA Mutation p.Gly129Arg(p.G129R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000262288
Start 57006184:57006184(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747888573
CDS Mutation c.1308C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000262288
Start 56998404:56998404(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766164757
CDS Mutation c.900C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000262288
Start 56981215:56981215(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.210G>T
Mutation Classification Silent
Feature Type Transcript