ANKRD36C — 22 ClinVar variants
All ClinVar germline ANKRD36C variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 1 flagged for review →
21 Likely benign · 1 Uncertain significance
Full ANKRD36C gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 1
Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.
Predictors split 1
The independent predictors disagree with each other — read with care.
All ANKRD36C variants
Likely benign 21
- p.Asp1068= Single submitter
- p.Asp2046Asn Single submitter
- p.Asp742= Single submitter
- p.Asp966= Single submitter
- p.Gln2014= Single submitter
- p.His1888= Single submitter
- p.Ile1666= Single submitter
- p.Leu1582= Single submitter
- p.Leu1812= Single submitter
- p.Leu1816= Single submitter
- p.Leu1852= Single submitter
- p.Leu2051= Single submitter
- p.Leu33= Single submitter
- p.Leu768Ser Single submitter
- p.Phe461= Single submitter
- p.Ser2034= Single submitter
- p.Ser836= Single submitter
- p.Ser955= Single submitter
- p.Val1851= Single submitter
- p.Val430= Single submitter
- p.His1286Asp No assertion criteria EBV-positive nodal T- and NK-cell lymphoma
Uncertain significance 1
- p.Asp1960His Single submitter ⚠