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  Search Results: 1 unique variant retrieved.



  c.5581G>T
p.(Asp1861Tyr) (Legacy AA No.1842)
Variant Type:
Point
Domain:
A3
Sequence Context:
GAC > TAC
Variant Effect:
Missense
Location:
Exon 16
No of bases:
No. of cases reported:
2
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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