S14W (p.Ser14Trp) variant of MALT1 (Q9UDY8)
S14W (p.Ser14Trp) in MALT1 (Q9UDY8) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Inborn genetic diseases; Combined immunodeficiency due to MALT1 deficiency. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
S14W (p.Ser14Trp) variant details
- p.Ser14Trp
- rs941975162
- ClinGen CA300934661
- ClinVar RCV001052466
- ClinVar RCV003346282
- Uncertain significance
- Inborn genetic diseases; Combined immunodeficiency due to MALT1 deficiency
- Missense
- Variant Prioritization Score for Impact Estimate 0.24
- CADD 15.80
- PolyPhen-2 0.19
- SIFT 0.02
- ClinVar: Uncertain significance (Inborn genetic diseases; Combined immunodeficiency due to MALT1)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the 1KG:LWK population (allele frequency 0.0058)
- Structural context available
- Cited in: Specific guidelines for assessing and improving the methodological quality of economic evaluations of newborn screening. (PMID 22947299)
- Cited in: Including the initial newborn screening bloodspot collection device serial number on birth certificates: basis and… (PMID 23037933)