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Search Results: 2 unique variants retrieved


Variant No. 142
p.(Pro206Ser) Legacy AA No. 188
Variant Type:
Point
Genomic:
15288C>T
Domain:
Apple 3
Codon Change:
CCT > TCT
Variant Effect:
Missense
Location:
Exon (7)
No of bases:
1
No. of cases reported:
3
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show

Variant No. 143
p.(Pro206Arg) Legacy AA No. 188
Variant Type:
Point
Genomic:
15289C>G
Domain:
Apple 3
Codon Change:
CCT > CGT
Variant Effect:
Missense
Location:
Exon (7)
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 structural information available.

Individual Case Information : Show