Variant (rsID / SNP)
rs4144901
rs4144901 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPAT. Location: chromosome 11, position 108,044,091. The table records no clinical significance for this variant.
Reference-table entries
NPATNot classified
- Variant type
- missense_variant
- Chromosome / position
- 11:108044091
- HGVS
- NM_001321307.1,c.1620A>T,p.Leu540Phe
- Allele change
- Missense_L540F
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.