Chromosome: | chr18 |
Position (hg19): | 21116665 |
Reference: | C |
Observed: | T |
Gene: | NPC1 |
Transcript: | NM_000271.4 |
Type: | missense_variant |
cDNA change: | c.3217G>A |
AA change: | p.Gly1073Ser |
Exon/intron: | 21 |
dbSNP id: | rs141440861 |
1000g AF: | |
ExAC AF: | 0.001458 |
ESP6500ea AF: | 0.0019 |
ESP6500aa AF: | 0.0005 |
Classification: | 1 (benign) |
# patients: | 0 |
# controls: | 18 |
Sources: | Exome_Variant_Server http://evs.gs.washington.edu/EVS/ |