SGCD NM_000337.6(SGCD):c.507G>A (p.Ala169=)

CI-VAR-00008757Explore in graph →p.Ala169=NM_000337.6:c.507G>AClinVar 48120 rs10071079

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
48120	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Qualitative or quantitative defects of delta-sarcoglycan; Cardiomyopathy; Autosomal recessive limb-girdle muscular dystrophy type 2F; Inborn genetic diseases; Dilated cardiomyopathy 1L; SGCD-related disorder; Uterine carcinosarcoma	germline	15	Feb 02, 2026	clinvar