| Chromosome: | chr18 |
| Position (hg19): | 21113447 |
| Reference: | C |
| Observed: | T |
| Gene: | NPC1 |
| Transcript: | NM_000271.4 |
| Type: | missense_variant |
| cDNA change: | c.3626G>A |
| AA change: | p.Gly1209Glu |
| Exon/intron: | 24 |
| dbSNP id: | |
| 1000g AF: | |
| ExAC AF: | 0.00001647 |
| ESP6500ea AF: | 0 |
| ESP6500aa AF: | 0.0002 |
| Classification: | 4 (likely pathogenic) |
| # patients: | 1 |
| # controls: | 0 |
| Sources: | Mac�as-Vidal_J_Clin_Genet_2011:_80:_39_�_49. http://www.ncbi.nlm.nih.gov/pubmed/20718790 |
