Search Results: 2 unique variants retrieved
c.6082G>T
p.(Gly2028Trp ) (Legacy AA No.2009)
Variant Type:
Point
Domain:
A3
Sequence Context:
GGG > TGG
Variant Effect:
Missense
Location:
Exon 19
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show
c.6082G>A
p.(Gly2028Arg) (Legacy AA No.2009)
Variant Type:
Point
Domain:
A3
Sequence Context:
GGG > AGG
Variant Effect:
Missense
Location:
Exon 19
No of bases:
1
No. of cases reported:
10
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show