| Chromosome: | chr18 |
| Position (hg19): | 21113341 |
| Reference: | G |
| Observed: | A |
| Gene: | NPC1 |
| Transcript: | NM_000271.4 |
| Type: | synonymous_variant |
| cDNA change: | c.3732C>T |
| AA change: | p.Leu1244Leu |
| Exon/intron: | 24 |
| dbSNP id: | rs1621962 |
| 1000g AF: | |
| ExAC AF: | 0.00006589 |
| ESP6500ea AF: | 0 |
| ESP6500aa AF: | 0.0007 |
| Classification: | 2 (likely benign) |
| # patients: | 1 |
| # controls: | 3 |
| Sources: | Exome_Variant_Server__Niemann-Pick_Type_C_Disease_Gene_Variation_Database NCBI_Entrez_SNP_database_(dbSNP_BUILD_127) |
