LOVD - Variant listings for TNFRSF10A

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Patient data (#0000073)
Patient ID
Disease -
Reference -
Template -
Technique -
Frequency -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
External ID dbSNP
Exon 8
DNA change c.889A>C   (View in UCSC Genome Browser, Ensembl)
Type Substitution
Mutation effect Missense
Protein p.(Asn297His)
PolyPhen 2 Probably damaging
Frequency A=0.981/C=0.019
DB-ID TNFRSF10A_00016

1 entry in TNFRSF10A

Path.
Allele Descending
Ascending
External ID Descending
Ascending
Exon 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 dbSNP 8 c.889A>C Substitution Missense p.(Asn297His) Probably damaging A=0.981/C=0.019 TNFRSF10A_00016