Search Results: 2 unique variants retrieved
c.535T>C
p.(Ser179Pro) (Legacy AA No.160)
Variant Type:
Point
Domain:
A1
Sequence Context:
TCT > CCT
Variant Effect:
Missense
Location:
Exon 4
No of bases:
1
No. of cases reported:
2
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show
c.536C>T
p.(Ser179Phe) (Legacy AA No.160)
Variant Type:
Point
Domain:
A1
Sequence Context:
TCT > TTT
Variant Effect:
Missense
Location:
Exon 4
No of bases:
No. of cases reported:
2
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show