N19K (p.Asn19Lys) variant of MYH11 (Myosin-11)
N19K (p.Asn19Lys) in MYH11 (Myosin-11) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Familial thoracic aortic aneurysm and aortic dissection. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
N19K (p.Asn19Lys) variant details
- p.Asn19Lys
- rs148464745
- ClinGen CA395198916
- ClinVar RCV001183946
- 1000Genomes rs148464745
- Uncertain significance
- Familial thoracic aortic aneurysm and aortic dissection
- Missense
- Variant Prioritization Score for Impact Estimate 0.265
- REVEL 0.25
- CADD 18.40
- PolyPhen-2 0.15
- SIFT 0.06
- ClinVar: Uncertain significance (Familial thoracic aortic aneurysm and aortic dissection)
- EBI: Benign
- UniProt: Benign
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available
- Cited in: Heritable Thoracic Aortic Disease Overview. (PMID 20301299)
- Cited in: Canadian Cardiovascular Society position statement on the management of thoracic aortic disease. (PMID 24882528)