Chromosome: | chr18 |
Position (hg19): | 21136474 |
Reference: | G |
Observed: | A |
Gene: | NPC1 |
Transcript: | NM_000271.4 |
Type: | synonymous_variant |
cDNA change: | c.1059C>T |
AA change: | p.Val353Val |
Exon/intron: | 8 |
dbSNP id: | rs138567139 |
1000g AF: | |
ExAC AF: | 0.00001647 |
ESP6500ea AF: | 0.0001 |
ESP6500aa AF: | 0.0118 |
Classification: | 2 (likely benign) |
# patients: | 0 |
# controls: | 1 |
Sources: | 1000Genome_Project http://www.1000genomes.org/ |