| Chromosome: | chr18 |
| Position (hg19): | 21118568 |
| Reference: | TCCCCCC |
| Observed: | T |
| Gene: | NPC1 |
| Transcript: | NM_000271.4 |
| Type: | disruptive_inframe_deletion |
| cDNA change: | c.2973_2978delGGGGGG |
| AA change: | p.Gly992_Gly993del |
| Exon/intron: | 20 |
| dbSNP id: | |
| 1000g AF: | |
| ExAC AF: | 0.000008236 |
| ESP6500ea AF: | 0.0008 |
| ESP6500aa AF: | 0.0002 |
| Classification: | 4 (likely pathogenic) |
| # patients: | 1 |
| # controls: | 0 |
| Sources: | Fern�ndez-Valero_E.M_(2005).__Clin_Genet._68_245�254 Fernandez-Valero_et_al._(2005)_Clin_Genet_68:245-254 |
