| Chromosome: | chr18 |
| Position (hg19): | 21121304 |
| Reference: | A |
| Observed: | C |
| Gene: | NPC1 |
| Transcript: | NM_000271.4 |
| Type: | missense_variant |
| cDNA change: | c.2339T>G |
| AA change: | p.Val780Gly |
| Exon/intron: | 15 |
| dbSNP id: | |
| 1000g AF: | |
| ExAC AF: | 0.00006589 |
| ESP6500ea AF: | 0.0001 |
| ESP6500aa AF: | 0 |
| Classification: | 4 (likely pathogenic) |
| # patients: | 1 |
| # controls: | 0 |
| Sources: | Fancello_et_al._(2009)_Neurogenetics_10:229-239 http://www.ncbi.nlm.nih.gov/pubmed/19252935 |
