Chromosome: | chr18 |
Position (hg19): | 21116646 |
Reference: | A |
Observed: | G |
Gene: | NPC1 |
Transcript: | NM_000271.4 |
Type: | missense_variant |
cDNA change: | c.3236T>C |
AA change: | p.Phe1079Ser |
Exon/intron: | 21 |
dbSNP id: | |
1000g AF: | |
ExAC AF: | 0.00001647 |
ESP6500ea AF: | 0 |
ESP6500aa AF: | 0.0002 |
Classification: | 4 (likely pathogenic) |
# patients: | 1 |
# controls: | 0 |
Sources: | Mac�as-Vidal_J_Clin_Genet_2011:_80:_39_�_49. http://www.ncbi.nlm.nih.gov/pubmed/20718790 |