Most severe consequence
12
Missense variant
Alleles
C/G|Ancestral: C|Highest population MAF: < 0.01
Location
Chromosome 1:150579012 (forward strand)|View in location tab
HGVS names
This variant has 11 HGVS names - Show
Synonyms
Uniprot VAR_024021
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 5 transcripts, 1 regulatory feature and has 2 sample genotypes.
