| Chromosome: | chr18 |
| Position (hg19): | 21134769 |
| Reference: | G |
| Observed: | C |
| Gene: | NPC1 |
| Transcript: | NM_000271.4 |
| Type: | missense_variant |
| cDNA change: | c.1506C>G |
| AA change: | p.Asp502Glu |
| Exon/intron: | 9 |
| dbSNP id: | rs191537721 |
| 1000g AF: | |
| ExAC AF: | 0.00006589 |
| ESP6500ea AF: | 0.0001 |
| ESP6500aa AF: | 0.0093 |
| Classification: | 2 (likely benign) |
| # patients: | 0 |
| # controls: | 1 |
| Sources: | 1000Genome_Project http://www.1000genomes.org/ |
