| Chromosome: | chr18 |
| Position (hg19): | 21125039 |
| Reference: | T |
| Observed: | C |
| Gene: | NPC1 |
| Transcript: | NM_000271.4 |
| Type: | missense_variant |
| cDNA change: | c.1832A>G |
| AA change: | p.Asp611Gly |
| Exon/intron: | 12 |
| dbSNP id: | rs483352887 |
| 1000g AF: | |
| ExAC AF: | 0.00005765 |
| ESP6500ea AF: | 0 |
| ESP6500aa AF: | 0.0005 |
| Classification: | 4 (likely pathogenic) |
| # patients: | 3 |
| # controls: | 0 |
| Sources: | Lin_et_al__J_Lipid_Res._201455(2):338-4__Zech_(2013)__PLoS_One__Zhang_et_al_2014 http://www.ncbi.nlm.nih.gov/pubmed/24190732 |
