Chromosome: | chr18 |
Position (hg19): | 21114516 |
Reference: | C |
Observed: | A |
Gene: | NPC1 |
Transcript: | NM_000271.4 |
Type: | missense_variant |
cDNA change: | c.3485G>T |
AA change: | p.Gly1162Val |
Exon/intron: | 23 |
dbSNP id: | |
1000g AF: | |
ExAC AF: | 0.000008237 |
ESP6500ea AF: | 0 |
ESP6500aa AF: | 0.0005 |
Classification: | 4 (likely pathogenic) |
# patients: | 1 |
# controls: | 0 |
Sources: | Harzer_(2014)_JIMD_Rep_12:25 na |