WDPCP NM_015910.7(WDPCP):c.160G>A (p.Asp54Asn)

CI-VAR-00025708Explore in graph →p.Asp54AsnNM_015910.7:c.160G>AClinVar 162669 rs200322968

Curated evidence

Evidence by cancer (0 items)

Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.

Data not yet available

No curated evidence item references this variant yet.

ClinVar

Clinical significance (1)

ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
162669	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Heart defect - tongue hamartoma - polysyndactyly syndrome; Orofaciodigital syndrome; Bardet-Biedl syndrome; WDPCP-related disorder; Bardet-Biedl syndrome 15; Melanoma; Retinal disorder; Fetal anomalies with a likely genetic cause	germline	13	Jun 30, 2026	clinvar