Primary Site >> Pancreatic Cancer

Gene >> DYSF

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000258104
Start 71669655:71669655(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143939123
CDS Mutation c.5576G>A
AA Mutation p.Arg1859His(p.R1859H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000258104
Start 71513873:71513873(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.615T>A
AA Mutation p.Ser205Arg(p.S205R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000258104
Start 71515714:71515714(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs398123802
CDS Mutation c.755C>T
AA Mutation p.Thr252Met(p.T252M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000258104
Start 71598686:71598686(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3643G>A
AA Mutation p.Ala1215Thr(p.A1215T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000258104
Start 71656280:71656280(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4628G>T
AA Mutation p.Gly1543Val(p.G1543V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000258104
Start 71568247:71568247(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2719G>A
AA Mutation p.Val907Ile(p.V907I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000258104
Start 71570642:71570642(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3075G>A
Mutation Classification Silent
Feature Type Transcript