Chromosome: | chr18 |
Position (hg19): | 21119808 |
Reference: | T |
Observed: | G |
Gene: | NPC1 |
Transcript: | NM_000271.4 |
Type: | missense_variant |
cDNA change: | c.2762A>C |
AA change: | p.Gln921Pro |
Exon/intron: | 18 |
dbSNP id: | |
1000g AF: | |
ExAC AF: | 0.00004942 |
ESP6500ea AF: | 0.0001 |
ESP6500aa AF: | 0 |
Classification: | 5 (pathogenic) |
# patients: | 4 |
# controls: | 0 |
Sources: | Fancello_et_al._(2009)_Neurogenetics_10:229-239 http://www.ncbi.nlm.nih.gov/pubmed/19252935 |