MYH14 NM_001145809.2(MYH14):c.3468-3C>T

CI-VAR-00008542Explore in graph →NM_001145809.2:c.3468-3C>TClinVar 44066 rs78192108

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
44066	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Autosomal dominant nonsyndromic hearing loss 4A; Uterine carcinosarcoma; Melanoma; Cholangiocarcinoma; Malignant tumor of esophagus; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Adrenocortical carcinoma, hereditary; Cervical cancer; Colorectal cancer; Lung cancer; Familial cancer of breast	germline/somatic	13	Feb 02, 2026	clinvar