LOVD - Variant listings for TNFRSF10B

About this overview [Show]

Patient data (#0000036)
Patient ID
Disease -
Reference -
Template -
Technique -
Frequency -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
Exon 5
DNA change c.677T>C   (View in UCSC Genome Browser, Ensembl)
External ID 1000 Genomes
Type Substitution
Mutation effect Missense
Protein p.(Ile226Thr)
PolyPhen 2 Benign
Frequency -
DB-ID TNFRSF10B_00031

1 entry in TNFRSF10B

Path.
Allele Descending
Ascending
Exon Descending
Ascending
DNA change Descending
Ascending
External ID Descending
Ascending
Type Descending
Ascending
Mutation effect Descending
Ascending
Protein Descending
Ascending
PolyPhen 2 Descending
Ascending
Frequency Descending
Ascending
DB-ID Descending
Ascending
?/? Unknown 5 c.677T>C 1000 Genomes Substitution Missense p.(Ile226Thr) Benign - TNFRSF10B_00031