| Chromosome: | chr18 |
| Position (hg19): | 21116826 |
| Reference: | T |
| Observed: | C |
| Gene: | NPC1 |
| Transcript: | NM_000271.4 |
| Type: | missense_variant |
| cDNA change: | c.3056A>G |
| AA change: | p.Tyr1019Cys |
| Exon/intron: | 21 |
| dbSNP id: | rs781261962 |
| 1000g AF: | |
| ExAC AF: | 0.000008236 |
| ESP6500ea AF: | 0 |
| ESP6500aa AF: | 0.0002 |
| Classification: | 5 (pathogenic) |
| # patients: | 4 |
| # controls: | 0 |
| Sources: | Fancello_et_al._(2009)_Neurogenetics_10:229-239 http://www.ncbi.nlm.nih.gov/pubmed/19252935 |
