Search Results: 2 unique variants retrieved
c.1468A>G
p.(Arg490Gly) (Legacy AA No.471)
Variant Type:
Point
Domain:
A2
Sequence Context:
AGA > GGA
Variant Effect:
Missense
Location:
Exon 10
No of bases:
1
No. of cases reported:
4
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
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c.1470A>T
p.(Arg490Ser) (Legacy AA No.471)
Variant Type:
Point
Domain:
A2
Sequence Context:
AGA > AGT
Variant Effect:
Missense
Location:
Exon 10
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show