LOVD - Variant listings for TNFRSF10D

About this overview [Show]

Patient data (#0000168)
Patient ID
Disease -
Reference -
Template -
Technique -
Frequency -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
Exon 9
External ID 1000 Genomes
DNA change c.1154G>A
Type Substitution
Mutation effect Missense
Protein p.(Cys385Tyr)
PolyPhen 2 Possibly damaging
Frequency -
DB-ID TNFRSF10D_00020

1 entry in TNFRSF10D

Path.
Allele Descending
Ascending
Exon Descending
Ascending
External ID Descending
Ascending
DNA change Descending
Ascending
Type Descending
Ascending
Mutation effect Descending
Ascending
Protein Descending
Ascending
PolyPhen 2 Descending
Ascending
Frequency Descending
Ascending
DB-ID Descending
Ascending
?/? Unknown 9 1000 Genomes c.1154G>A Substitution Missense p.(Cys385Tyr) Possibly damaging - TNFRSF10D_00020