Data Display Options:

UNIQUE (Without Case Data) :
MULTIPLE (With Case Data) :

  Search Results: 2 unique variants retrieved



  c.5809T>G
p.(Phe1937Val) (Legacy AA No.1918)
Variant Type:
Point
Domain:
A3
Sequence Context:
TTC > GTC
Variant Effect:
Missense
Location:
Exon 17
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is the available information.

Individual Case Information : Show


  c.5810T>C
p.(Phe1937Ser) (Legacy AA No.1918)
Variant Type:
Point
Domain:
A3
Sequence Context:
TTC > TCC
Variant Effect:
Missense
Location:
Exon 17
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is the available information.

Individual Case Information : Show