LOVD - Variant listings for TNFRSF10D

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Patient data (#0000141)
Patient ID
Disease -
Reference -
Template -
Technique -
Frequency -
Remarks -

Variant data
Allele Unknown
Reported pathogenicity -
Concluded pathogenicity Unknown
Exon 9
External ID NHLBI Exome Sequencing Project
DNA change c.1139G>T
Type Substitution
Mutation effect Missense
Protein p.(Gly380Val)
PolyPhen 2 Probably damaging
Frequency A=1/C=10757
DB-ID TNFRSF10D_00001

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 9 NHLBI Exome Sequencing Project c.1139G>T Substitution Missense p.(Gly380Val) Probably damaging A=1/C=10757 TNFRSF10D_00001