Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.861C>T
p.Ile287= (Legacy AA No. 269)
Variant Type:
Point
Domain:
Linker
Codon Change:
C>T
Variant Effect:
Silent
No. of Patients Reported:
0
Phenotype:
None
Allele Count *:
281
Allele Number *:
282734
Allele Frequency *:
0.000994