Primary Site >> Esophagus Cancer

Gene >> ELMO1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000310758
Start 37211471:37211471(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1001C>T
AA Mutation p.Ala334Val(p.A334V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000310758
Start 37224921:37224921(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776057144
CDS Mutation c.659C>T
AA Mutation p.Ala220Val(p.A220V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000310758
Start 37211426:37211426(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1046A>G
AA Mutation p.Lys349Arg(p.K349R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000310758
Start 37211468:37211468(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1004A>G
AA Mutation p.Glu335Gly(p.E335G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000310758
Start 37216658:37216658(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.818C>T
AA Mutation p.Ser273Phe(p.S273F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000310758
Start 36894961:36894961(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1494C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000310758
Start 36894880:36894880(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1575G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000310758
Start 37314901:37314901(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.141A>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000310758
Start 37342685:37342685(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6G>T
Mutation Classification Silent
Feature Type Transcript