Primary Site >> Stomach Cancer

Gene >> ECHS1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368547
Start 133370722:133370722(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.124G>T
AA Mutation p.Gly42Trp(p.G42W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368547
Start 133366027:133366027(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.688G>A
AA Mutation p.Ala230Thr(p.A230T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368547
Start 133366038:133366038(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.677C>T
AA Mutation p.Ala226Val(p.A226V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368547
Start 133366033:133366033(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.682A>C
AA Mutation p.Lys228Gln(p.K228Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000368547
Start 133366064:133366064(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.651A>G
Mutation Classification Silent
Feature Type Transcript