Primary Site >> Esophagus Cancer

Gene >> FLT1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000282397
Start 28385022:28385022(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1979C>A
AA Mutation p.Ala660Glu(p.A660E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000282397
Start 28322865:28322865(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs554058758
CDS Mutation c.2878G>A
AA Mutation p.Val960Ile(p.V960I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000282397
Start 28306690:28306690(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368266056
CDS Mutation c.3803C>T
AA Mutation p.Ser1268Leu(p.S1268L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000282397
Start 28438272:28438272(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.462C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000282397
Start 28334122:28334122(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2496A>C
Mutation Classification Silent
Feature Type Transcript