LOVD - Variant listings for TNFRSF10D

About this overview [Show]

Patient data (#0000156)
Patient ID
Disease -
Reference -
Template -
Technique -
Frequency -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
Exon 7
External ID dbSNP
DNA change c.872G>C
Type Substitution
Mutation effect Missense
Protein p.(Ser291Cys)
PolyPhen 2 Probably damaging
Frequency G=0.989/C=0.011
DB-ID TNFRSF10D_00008

1 entry in TNFRSF10D

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 7 dbSNP c.872G>C Substitution Missense p.(Ser291Cys) Probably damaging G=0.989/C=0.011 TNFRSF10D_00008