Chromosome: | chr18 |
Position (hg19): | 21112371 |
Reference: | G |
Observed: | A |
Gene: | NPC1 |
Transcript: | NM_000271.4 |
Type: | intron_variant |
cDNA change: | c.3755-123C>T |
AA change: | |
Exon/intron: | 24 |
dbSNP id: | |
1000g AF: | |
ExAC AF: | 0.001054 |
ESP6500ea AF: | 0.0013 |
ESP6500aa AF: | 0 |
Classification: | 3 (unknown significance) |
# patients: | 1 |
# controls: | 0 |
Sources: | Niemann-Pick_Type_C_Disease_Gene_Variation_Database Morris_et_al._(1999)_Biochem_Biophys_Res_Commun_261:493-498 |