Search Results: 2 unique variants retrieved
c.2213A>G
p.(Tyr738Cys) (Legacy AA No.719)
Variant Type:
Point
Domain:
A2
Sequence Context:
TAC > TGC
Variant Effect:
Missense
Location:
Exon 14
No of bases:
1
No. of cases reported:
2
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
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c.2214C>G
p.(Tyr738*) (Legacy AA No.719)
Variant Type:
Point
Domain:
A2
Sequence Context:
TAC > TAG
Variant Effect:
Nonsense
Location:
Exon 14
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Structural Analysis cannot be performed for this type (Point | Nonsense) of mutation at Exon 14
Individual Case Information :
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