| Chromosome: | chr18 |
| Position (hg19): | 21118573 |
| Reference: | C |
| Observed: | T |
| Gene: | NPC1 |
| Transcript: | NM_000271.4 |
| Type: | missense_variant |
| cDNA change: | c.2974G>A |
| AA change: | p.Gly992Arg |
| Exon/intron: | 20 |
| dbSNP id: | rs80358254 |
| 1000g AF: | |
| ExAC AF: | 0.000008236 |
| ESP6500ea AF: | 0.0001 |
| ESP6500aa AF: | 0 |
| Classification: | 3 (unknown significance) |
| # patients: | 1 |
| # controls: | 0 |
| Sources: | Niemann-Pick_Type_C_Disease_Gene_Variation_Database Millat_et_al._(2001)_Am_J_Hum_Genet_69:1013-1021 |
