| Chromosome: | chr18 |
| Position (hg19): | 21140384 |
| Reference: | A |
| Observed: | C |
| Gene: | NPC1 |
| Transcript: | NM_000271.4 |
| Type: | missense_variant |
| cDNA change: | c.692T>G |
| AA change: | p.Val231Gly |
| Exon/intron: | 6 |
| dbSNP id: | |
| 1000g AF: | |
| ExAC AF: | 0.00003295 |
| ESP6500ea AF: | 0.0004 |
| ESP6500aa AF: | 0 |
| Classification: | 3 (unknown significance) |
| # patients: | 1 |
| # controls: | 0 |
| Sources: | Niemann-Pick_Type_C_Disease_Gene_Variation_Database Kaminski_et_al._(2002)_J_Inherit_Metab_Dis_25:385-389 |
