LOVD - Variant listings for TNFRSF10C

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Patient data (#0000146)
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.242A>G   (View in UCSC Genome Browser, Ensembl)
Type Substitution
Mutation effect Missense
Protein p.(Asn81Ser)
PolyPhen 2 Probably damaging
Frequency A=0.998/G=0.002
DB-ID TNFRSF10C_00006

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.242A>G Substitution Missense p.(Asn81Ser) Probably damaging A=0.998/G=0.002 TNFRSF10C_00006