Search Results: 2 unique variants retrieved
c.1364T>G
p.(Phe455Cys) (Legacy AA No.436)
Variant Type:
Point
Domain:
A2
Sequence Context:
TTT > TGT
Variant Effect:
Missense
Location:
Exon 9
No of bases:
1
No. of cases reported:
3
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show
c.1364T>C
p.(Phe455Ser) (Legacy AA No.436)
Variant Type:
Point
Domain:
A2
Sequence Context:
TTT > TCT
Variant Effect:
Missense
Location:
Exon 9
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show