LOVD - Variant listings for TNFRSF10C

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Patient data (#0000143)
Patient ID
Disease -
Reference -
Template -
Technique -
Frequency -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
Exon 3
External ID dbSNP
DNA change c.172C>G   (View in UCSC Genome Browser, Ensembl)
Type Substitution
Mutation effect Missense
Protein p.(His58Asp)
PolyPhen 2 Probably damaging
Frequency C=0.999/G=0.001
DB-ID TNFRSF10C_00003

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 3 dbSNP c.172C>G Substitution Missense p.(His58Asp) Probably damaging C=0.999/G=0.001 TNFRSF10C_00003