LOVD - Variant listings for TNFRSF10C

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Patient data (#0000149)
Patient ID
Disease -
Reference -
Template -
Technique -
Frequency -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
Exon 5
External ID dbSNP
DNA change c.514C>T   (View in UCSC Genome Browser, Ensembl)
Type Substitution
Mutation effect Missense
Protein p.(Pro172Ser)
PolyPhen 2 Possibly damaging
Frequency C=0.993/T=0.007
DB-ID TNFRSF10C_00009

1 entry in TNFRSF10C

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 5 dbSNP c.514C>T Substitution Missense p.(Pro172Ser) Possibly damaging C=0.993/T=0.007 TNFRSF10C_00009