Search Results: 2 unique variants retrieved
c.1984G>A
p.(Gly662Arg) (Legacy AA No.643)
Variant Type:
Point
Domain:
A2
Sequence Context:
GGA > AGA
Variant Effect:
Missense
Location:
Exon 13
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show
c.1985G>C
p.(Gly662Ala) (Legacy AA No.643)
Variant Type:
Point
Domain:
A2
Sequence Context:
GGA > GCA
Variant Effect:
Missense
Location:
Exon 13
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show