LOVD - Variant listings for TNFRSF10D

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Patient data (#0000170)
Patient ID
Disease -
Reference -
Template -
Technique -
Frequency -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
Exon 2
External ID 1000 Genomes
DNA change c.186C>G
Type Substitution
Mutation effect Missense
Protein p.(Asp62Glu)
PolyPhen 2 Possibly damaging
Frequency -
DB-ID TNFRSF10D_00021

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 2 1000 Genomes c.186C>G Substitution Missense p.(Asp62Glu) Possibly damaging - TNFRSF10D_00021