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  Search Results: 2 unique variants retrieved



  c.6454_6455delTCinsATAT
p.(Ser2152Ilefs*4) (Legacy AA No.2133)
Variant Type:
Indel
Domain:
C1
Sequence Context:
Variant Effect:
Frameshift
Location:
Exon 23
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 (Indel | Frameshift) of mutation at Exon 23

Individual Case Information : Show


  c.6454T>C
p.(Ser2152Pro) (Legacy AA No.2133)
Variant Type:
Point
Domain:
C1
Sequence Context:
TCT > CCT
Variant Effect:
Missense
Location:
Exon 23
No of bases:
1
No. of cases reported:
2
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show