Data Display Options:

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

  Search Results: 2 unique variants retrieved



  c.1825A>T
p.(Asn609Tyr) (Legacy AA No.590)
Variant Type:
Point
Domain:
A2
Sequence Context:
AAT > TAT
Variant Effect:
Missense
Location:
Exon 12
No of bases:
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.1826A>T
p.(Asn609Ile) (Legacy AA No.590)
Variant Type:
Point
Domain:
A2
Sequence Context:
AAT > ATT
Variant Effect:
Missense
Location:
Exon 12
No of bases:
1
No. of cases reported:
5
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is the available information.

Individual Case Information : Show