Chromosome: | chr18 |
Position (hg19): | 21136478 |
Reference: | C |
Observed: | A |
Gene: | NPC1 |
Transcript: | NM_000271.4 |
Type: | missense_variant |
cDNA change: | c.1055G>T |
AA change: | p.Cys352Phe |
Exon/intron: | 8 |
dbSNP id: | rs149020783 |
1000g AF: | |
ExAC AF: | 0.00001647 |
ESP6500ea AF: | 0.0002 |
ESP6500aa AF: | 0 |
Classification: | 2 (likely benign) |
# patients: | 0 |
# controls: | 2 |
Sources: | Exome_Variant_Server http://evs.gs.washington.edu/EVS/ |