Chromosome: | chr18 |
Position (hg19): | 21140158 |
Reference: | G |
Observed: | C |
Gene: | NPC1 |
Transcript: | NM_000271.4 |
Type: | intron_variant |
cDNA change: | c.881+37C>G |
AA change: | |
Exon/intron: | 6 |
dbSNP id: | rs142700149 |
1000g AF: | |
ExAC AF: | 0.00103 |
ESP6500ea AF: | 0 |
ESP6500aa AF: | 0.012 |
Classification: | 1 (benign) |
# patients: | 0 |
# controls: | 53 |
Sources: | Exome_Variant_Server http://evs.gs.washington.edu/EVS/ |