| Chromosome: | chr18 |
| Position (hg19): | 21119914 |
| Reference: | C |
| Observed: | G |
| Gene: | NPC1 |
| Transcript: | NM_000271.4 |
| Type: | missense_variant |
| cDNA change: | c.2656G>C |
| AA change: | p.Gly886Arg |
| Exon/intron: | 18 |
| dbSNP id: | |
| 1000g AF: | |
| ExAC AF: | 0.001828 |
| ESP6500ea AF: | 0 |
| ESP6500aa AF: | 0.015 |
| Classification: | 4 (likely pathogenic) |
| # patients: | 1 |
| # controls: | 0 |
| Sources: | Niemann-Pick_Type_C_Disease_Gene_Variation_Database Imrie_et_al._(2007)_J_Inherit_Metab_Dis_30:51-59 |
