Search Results: 2 unique variants retrieved
c.5809T>G
p.(Phe1937Val) (Legacy AA No.1918)
Variant Type:
Point
Domain:
A3
Sequence Context:
TTC > GTC
Variant Effect:
Missense
Location:
Exon 17
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
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c.5810T>C
p.(Phe1937Ser) (Legacy AA No.1918)
Variant Type:
Point
Domain:
A3
Sequence Context:
TTC > TCC
Variant Effect:
Missense
Location:
Exon 17
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show