Data Display Options:

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

  Search Results: 4 unique variants retrieved



  c.1702G>T
p.(Gly568Cys) (Legacy AA No.549)
Variant Type:
Point
Domain:
A2
Sequence Context:
GGC > TGC
Variant Effect:
Missense
Location:
Exon 11
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.1702G>A
p.(Gly568Ser) (Legacy AA No.549)
Variant Type:
Point
Domain:
A2
Sequence Context:
GGC > AGC
Variant Effect:
Missense
Location:
Exon 11
No of bases:
1
No. of cases reported:
3
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is the available information.

Individual Case Information : Show


  c.1703G>A
p.(Gly568Asp) (Legacy AA No.549)
Variant Type:
Point
Domain:
A2
Sequence Context:
GGC > GAC
Variant Effect:
Missense
Location:
Exon 11
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.1703G>T
p.(Gly568Val) (Legacy AA No.549)
Variant Type:
Point
Domain:
A2
Sequence Context:
GGC > GTC
Variant Effect:
Missense
Location:
Exon 11
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