Most severe consequence
13
missense variant
Alleles
G/C/T|Highest population MAF: 0.50
Location
Chromosome 10:1474937 (forward strand)|VCF:10 1474937 ENSVVVI00603001 G C,T
HGVS names
This variant has 6 HGVS names - Show
External Links
Original source
Cold Spring Harbor Laboratory / Cornell University [[remapped to PN40024.v4] (release 1)
About this variant
This variant overlaps 1 transcript and has 11 sample genotypes.
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