| Chromosome: | chr18 |
| Position (hg19): | 21114440 |
| Reference: | C |
| Observed: | A |
| Gene: | NPC1 |
| Transcript: | NM_000271.4 |
| Type: | synonymous_variant |
| cDNA change: | c.3561G>T |
| AA change: | p.Ala1187Ala |
| Exon/intron: | 23 |
| dbSNP id: | rs55724504 |
| 1000g AF: | |
| ExAC AF: | 0.002487 |
| ESP6500ea AF: | 0.0029 |
| ESP6500aa AF: | 0.002 |
| Classification: | 1 (benign) |
| # patients: | 1 |
| # controls: | 34 |
| Sources: | Exome_Variant_Server__Niemann-Pick_Type_C_Disease_Gene_Variation_Database Fernandez-Valero_et_al._(2005)_Clin_Genet_68:245-254 |
