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Search Results: 2 unique variants retrieved


Variant No. 219
p.(Cys339Phe) Legacy AA No. 321
Variant Type:
Point
Genomic:
19410G>T
Domain:
Apple 4
Codon Change:
TGC > TTC
Variant Effect:
Missense
Location:
Exon (9)
No of bases:
1
No. of cases reported:
2
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show

Variant No. 218
p.(Cys339Ser) Legacy AA No. 321
Variant Type:
Point
Genomic:
19410G>C
Domain:
Apple 4
Codon Change:
TGC > TCC
Variant Effect:
Missense
Location:
Exon (9)
No of bases:
1
No. of cases reported:
0
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is structural information available.

Individual Case Information : Show