Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.67C>T
p.Gln23* (Legacy AA No. 5)
Variant Type:
Point
Domain:
Apple 1
Codon Change:
C>T
Variant Effect:
Nonsense
No. of Patients Reported:
0
Phenotype:
U
Allele Count *:
3
Allele Number *:
251420
Allele Frequency *:
0.000012