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Search Results: 2 unique variants retrieved


Variant No. 13
p.(Met1?) Legacy AA No. -18
Variant Type:
Point
Genomic:
6175T>A
Domain:
Signal Peptide
Codon Change:
ATG > AAT
Variant Effect:
Missense
Location:
Exon (2)
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show

Variant No. 14
p.(Met1?) Legacy AA No. -18
Variant Type:
Point
Genomic:
6176G>T
Domain:
Signal Peptide
Codon Change:
ATG > ATT
Variant Effect:
Missense
Location:
Exon (2)
No of bases:
1
No. of cases reported:
4
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is structural information available.

Individual Case Information : Show