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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9P2D1: Variant p.Arg2065Ser

Chromodomain-helicase-DNA-binding protein 7
Gene: CHD7
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Variant information Variant position: help 2065 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] The variants are classified into three categories: LP/P, LB/B and US.
  • LP/P: likely pathogenic or pathogenic.
  • LB/B: likely benign or benign.
  • US: uncertain significance
Residue change: help From Arginine (R) to Serine (S) at position 2065 (R2065S, p.Arg2065Ser). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties: help Change from large size and basic (R) to small size and polar (S) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -1 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page
Variant description: help In CHARGES. Any additional useful information about the variant.


Sequence information Variant position: help 2065 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 2997 The length of the canonical sequence.
Location on the sequence: help PITEERASRTLYRIELLRKI R EQVLHHPQLGERLKLCQPSL The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: help The multiple alignment of the region surrounding the variant against various orthologous sequences. 
Human                         PITEERASRTLYRIELLRKIREQVLHHPQLGERLKLCQPSL

Mouse                         PITEERASRTLYRIELLRKIREQVLHHPQLSDRLKLCQPSL

Chicken                       PITEERASRTLYRIELLRKIREQVLHHPQLGERLKLCQPSL
Sequence annotation in neighborhood: help The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
  • Type: the type of sequence feature.
  • Positions: endpoints of the sequence feature.
  • Description: contains additional information about the feature.
TypePositionsDescription
Chain 1 – 2997 Chromodomain-helicase-DNA-binding protein 7
Alternative sequence 572 – 2620 Missing. In isoform 4.
Alternative sequence 834 – 2620 Missing. In isoform 3.
Alternative sequence 1139 – 2997 Missing. In isoform 2.



Literature citations
CHD7 mutational analysis and clinical considerations for auditory rehabilitation in deaf patients with CHARGE syndrome.
Song M.H.; Cho H.J.; Lee H.K.; Kwon T.J.; Lee W.S.; Oh S.; Bok J.; Choi J.Y.; Kim U.K.;
PLoS ONE 6:E24511-E24511(2011)
Cited for: VARIANT CHARGES SER-2065;
Disclaimer: Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.