Search Results: 3 unique variants retrieved
c.934_935delTT
p.(Phe312Profs*25) (Legacy AA No.293)
Variant Type:
Deletion
Domain:
A1
Sequence Context:
Variant Effect:
Frameshift
Location:
Exon 7
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Structural Analysis cannot be performed for this type (Deletion | Frameshift) of mutation at Exon 7
Individual Case Information :
Show
(presumed 1-st) |
(2-st/Chr) |
(1-st/2-st) |
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---|---|---|---|---|---|---|---|---|---|---|
c.935T>C
p.(Phe312Ser) (Legacy AA No.293)
Variant Type:
Point
Domain:
A1
Sequence Context:
TTC > TCC
Variant Effect:
Missense
Location:
Exon 7
No of bases:
1
No. of cases reported:
38
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show
(presumed 1-st) |
(2-st/Chr) |
(1-st/2-st) |
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---|---|---|---|---|---|---|---|---|---|---|
c.935delT
p.(Phe312Serfs*8) (Legacy AA No.293)
Variant Type:
Deletion
Domain:
A1
Sequence Context:
Variant Effect:
Frameshift
Location:
Exon 7
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 (Deletion | Frameshift) of mutation at Exon 7
Individual Case Information :
Show
(presumed 1-st) |
(2-st/Chr) |
(1-st/2-st) |
||||||||
---|---|---|---|---|---|---|---|---|---|---|