Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.1084G>A
p.Gly362Arg (Legacy AA No. 344)
Variant Type:
Point
Domain:
Apple 4
Codon Change:
Variant Effect:
Missense
No. of Patients Reported:
1
Phenotype:
U
Allele Count *:
22
Allele Number *:
282750
Allele Frequency *:
0.000078