Chromosome: | chr18 |
Position (hg19): | 21114435 |
Reference: | T |
Observed: | C |
Gene: | NPC1 |
Transcript: | NM_000271.4 |
Type: | missense_variant |
cDNA change: | c.3566A>G |
AA change: | p.Glu1189Gly |
Exon/intron: | 23 |
dbSNP id: | rs369098773 |
1000g AF: | |
ExAC AF: | 0.00001647 |
ESP6500ea AF: | 0.0001 |
ESP6500aa AF: | 0 |
Classification: | 4 (likely pathogenic) |
# patients: | 1 |
# controls: | 1 |
Sources: | Exome_Variant_Server__Niemann-Pick_Type_C_Disease_Gene_Variation_Database Sun_et_al._(2001)_Am_J_Hum_Genet_68:1361-1372 |