| Chromosome: | chr18 |
| Position (hg19): | 21140203 |
| Reference: | C |
| Observed: | A |
| Gene: | NPC1 |
| Transcript: | NM_000271.4 |
| Type: | missense_variant |
| cDNA change: | c.873G>T |
| AA change: | p.Trp291Cys |
| Exon/intron: | 6 |
| dbSNP id: | rs138151007 |
| 1000g AF: | |
| ExAC AF: | 0.0000906 |
| ESP6500ea AF: | 0.0001 |
| ESP6500aa AF: | 0.0014 |
| Classification: | 3 (unknown significance) |
| # patients: | 0 |
| # controls: | 7 |
| Sources: | Exome_Variant_Server http://evs.gs.washington.edu/EVS/ |
