Data Display Options:

UNIQUE (Without Case Data) :
MULTIPLE (With Case Data) :

  Search Results: 4 unique variants retrieved



  c.6520C>G
p.(His2174Asp) (Legacy AA No.2155)
Variant Type:
Point
Domain:
C1
Sequence Context:
CAT > GAT
Variant Effect:
Missense
Location:
Exon 23
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 the available information.

Individual Case Information : Show


  c.6520C>T
p.(His2174Tyr) (Legacy AA No.2155)
Variant Type:
Point
Domain:
C1
Sequence Context:
CAT > TAT
Variant Effect:
Missense
Location:
Exon 23
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 the available information.

Individual Case Information : Show


  c.6521A>G
p.(His2174Arg) (Legacy AA No.2155)
Variant Type:
Point
Domain:
C1
Sequence Context:
CAT > CGT
Variant Effect:
Missense
Location:
Exon 23
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is the available information.

Individual Case Information : Show


  c.6521A>C
p.(His2174Pro) (Legacy AA No.2155)
Variant Type:
Point
Domain:
C1
Sequence Context:
CAT > CCT
Variant Effect:
Missense
Location:
Exon 23
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is the available information.

Individual Case Information : Show