LOVD - Variant listings for TNFRSF10B

About this overview [Show]

Patient data (#0000001)
Patient ID
Disease -
Reference Lee et al., 2010
Template -
Technique -
Frequency -
Remarks This variant is associated with survival outcome in early-stage non-small-cell lung cancer (NSCLC).

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
Exon 2
DNA change c.200C>T   (View in UCSC Genome Browser, Ensembl)
External ID dbSNP
Type Substitution
Mutation effect Missense
Protein p.(Ala67Val)
PolyPhen 2 Possibly damaging
Frequency -
DB-ID TNFRSF10B_00001

1 entry in TNFRSF10B

Path.
Allele Descending
Ascending
Exon Descending
Ascending
DNA change Descending
Ascending
External ID Descending
Ascending
Type Descending
Ascending
Mutation effect Descending
Ascending
Protein Descending
Ascending
PolyPhen 2 Descending
Ascending
Frequency Descending
Ascending
DB-ID Descending
Ascending
?/? Unknown 2 c.200C>T dbSNP Substitution Missense p.(Ala67Val) Possibly damaging - TNFRSF10B_00001