Search Results: 2 unique variants retrieved
c.883T>A
p.(Phe295Ile) (Legacy AA No.276)
Variant Type:
Point
Domain:
A1
Sequence Context:
TTT > ATT
Variant Effect:
Missense
Location:
Exon 7
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show
c.883T>C
p.(Phe295Leu) (Legacy AA No.276)
Variant Type:
Point
Domain:
A1
Sequence Context:
TTT > CTT
Variant Effect:
Missense
Location:
Exon 7
No of bases:
1
No. of cases reported:
2
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show