Chromosome: | chr18 |
Position (hg19): | 21134704 |
Reference: | T |
Observed: | C |
Gene: | NPC1 |
Transcript: | NM_000271.4 |
Type: | splice_region_variant&intron_variant |
cDNA change: | c.1553+18A>G |
AA change: | |
Exon/intron: | 9 |
dbSNP id: | rs373017634 |
1000g AF: | |
ExAC AF: | 0.0003624 |
ESP6500ea AF: | 0.0007 |
ESP6500aa AF: | 0 |
Classification: | 2 (likely benign) |
# patients: | 0 |
# controls: | 6 |
Sources: | Exome_Variant_Server http://evs.gs.washington.edu/EVS/ |