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Search Results: 1 unique variant retrieved.


Variant No. 54
p.(Thr60Pro) (Legacy AA No. 42)
Variant Type:
Indel
Genomic:
10767_10768delinsTC
Codon Change:
ACT CCT
Variant Effect:
Missense
Location:
Exon 3
No of bases:
2
No. of cases reported:
3
Allele Frequency (MAF):
Domain:
Apple 1
Pathogenicity(ACMG): 2=Likely Benign, 3=Uncertain, 4=Likely Pathogenic:

Individual Case Information : Show