Chromosome: | chr18 |
Position (hg19): | 21115440 |
Reference: | A |
Observed: | G |
Gene: | NPC1 |
Transcript: | NM_000271.4 |
Type: | missense_variant |
cDNA change: | c.3470T>C |
AA change: | p.Leu1157Pro |
Exon/intron: | 22 |
dbSNP id: | |
1000g AF: | |
ExAC AF: | 0.0007825 |
ESP6500ea AF: | 0.0002 |
ESP6500aa AF: | 0.0059 |
Classification: | 4 (likely pathogenic) |
# patients: | 1 |
# controls: | 0 |
Sources: | Niemann-Pick_Type_C_Disease_Gene_Variation_Database Saraiva-Pereira__ML_unpublished_(personal_communication) |