Primary Site >> Esophagus Cancer

Gene >> VWF

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 5953516:5953516(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7966G>A
AA Mutation p.Gly2656Arg(p.G2656R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 6019369:6019369(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764155969
CDS Mutation c.4049C>T
AA Mutation p.Ala1350Val(p.A1350V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 6019475:6019475(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs61749395
CDS Mutation c.3943C>T
AA Mutation p.Arg1315Cys(p.R1315C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 6018979:6018979(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778742589
CDS Mutation c.4439C>T
AA Mutation p.Pro1480Leu(p.P1480L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 5994452:5994452(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6219C>A
AA Mutation p.Ser2073Arg(p.S2073R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000261405
Start 6057925:6057925(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1653C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000261405
Start 6073629:6073629(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.987C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000261405
Start 5952481:5952481(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8025C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000261405
Start 6018468:6018468(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4950C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000261405
Start 6044426:6044426(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2307C>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000261405
Start 6023647:6023647(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3363G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000261405
Start 5949801:5949801(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8238T>C
Mutation Classification Silent
Feature Type Transcript