Chromosome: | chr18 |
Position (hg19): | 21115414 |
Reference: | A |
Observed: | G |
Gene: | NPC1 |
Transcript: | NM_000271.4 |
Type: | splice_region_variant&intron_variant |
cDNA change: | c.3477+19T>C |
AA change: | |
Exon/intron: | 22 |
dbSNP id: | rs375942184 |
1000g AF: | |
ExAC AF: | 0.0001318 |
ESP6500ea AF: | 0.0005 |
ESP6500aa AF: | 0 |
Classification: | 2 (likely benign) |
# patients: | 0 |
# controls: | 4 |
Sources: | Exome_Variant_Server http://evs.gs.washington.edu/EVS/ |