Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.197C>T
p.Pro66Leu (Legacy AA No. 48)
Variant Type:
Point
Domain:
Apple 1
Codon Change:
C>T
Variant Effect:
Missense
No. of Patients Reported:
0
Phenotype:
None
Allele Count *:
18
Allele Number *:
282848
Allele Frequency *:
0.000064