LOVD - Variant listings for TNFRSF10A

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Patient data (#0000106)
Patient ID
Disease -
Reference -
Template -
Technique -
Frequency -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
External ID NHLBI Exome Sequencing Project
Exon 10
DNA change c.1135T>C   (View in UCSC Genome Browser, Ensembl)
Type Substitution
Mutation effect Missense
Protein p.(Ser379Pro)
PolyPhen 2 Probably damaging
Frequency C=1/T=10755
DB-ID TNFRSF10A_00049

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 NHLBI Exome Sequencing Project 10 c.1135T>C Substitution Missense p.(Ser379Pro) Probably damaging C=1/T=10755 TNFRSF10A_00049