IGHMBP2 NM_002180.3(IGHMBP2):c.1193C>T (p.Ala398Val)

CI-VAR-00037623Explore in graph →p.Ala398ValNM_002180.3:c.1193C>TClinVar 234315 rs35193202

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
234315	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Autosomal recessive distal spinal muscular atrophy 1; Charcot-Marie-Tooth disease axonal type 2S; Charcot-Marie-Tooth disease; Inborn genetic diseases; IGHMBP2-related disorder; Ovarian serous cystadenocarcinoma; Thyroid cancer, nonmedullary, 1; Melanoma; Malignant tumor of esophagus; Gastric cancer; Uterine carcinosarcoma	germline	14	Feb 01, 2026	clinvar