L48I (p.Leu48Ile) variant of DNMT1 (P26358)
L48I (p.Leu48Ile) in DNMT1 (P26358) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary sensory neuropathy-deafness-dementia syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes published literature and structural context.
L48I (p.Leu48Ile) variant details
- p.Leu48Ile
- rs2145379887
- ClinGen CA403947275
- ClinVar RCV001925968
- Ensembl rs2145379887
- Uncertain significance
- Hereditary sensory neuropathy-deafness-dementia syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.392
- AlphaMissense 0.14
- MetaLR 0.29
- MetaSVM -0.68
- PolyPhen-2 1.00
- SIFT 0.00
- MutPred 0.69
- ClinVar: Uncertain significance (Hereditary sensory neuropathy-deafness-dementia syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: Charcot-Marie-Tooth Hereditary Neuropathy Overview. (PMID 20301532)
- Cited in: DNMT1-Related Disorder. (PMID 22338191)