Primary Site >> Stomach Cancer

Gene >> STC1

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000290271
Start 23851321:23851321(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.472A>G
AA Mutation p.Arg158Gly(p.R158G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000290271
Start 23852372:23852372(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778423061
CDS Mutation c.131G>A
AA Mutation p.Arg44His(p.R44H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000290271
Start 23844792:23844792(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201521623
CDS Mutation c.722G>A
AA Mutation p.Arg241His(p.R241H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000290271
Start 23852347:23852347(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751715085
CDS Mutation c.156C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000290271
Start 23852287:23852287(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.216C>T
Mutation Classification Silent
Feature Type Transcript