UniProtKB/Swiss-Prot Q86VP6: Variant p.Ala952Val

Cullin-associated NEDD8-dissociated protein 1
Gene: CAND1
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Variant information Variant position:

952 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant:

LB/B 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:

From Alanine (A) to Valine (V) at position 952 (A952V, p.Ala952Val). 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:

Change from small size and hydrophobic (A) to medium size and hydrophobic (V) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

0 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
Other resources:

Links to websites of interest for the variant.

Variant rs17854618 [ dbSNP | Ensembl ]

Sequence information Variant position:

952 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:

1230 The length of the canonical sequence.
Location on the sequence:

IWALLLKHCECAEEGTRNVV A ECLGKLTLIDPETLLPRLKG 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:

The multiple alignment of the region surrounding the variant against various orthologous sequences.

Human                         IWALLLKHCECAEEGT----RNVVAECLGKLTLIDPETLLPRLKG

Mouse                         IWALLLKHCECAEEGT----RNVVAECLGKLTLIDPETLLP

Rat                           IWALLLKHCECAEEGT----RNVVAECLGKLTLIDPETLLP

Bovine                        IWALLLKHCECAEEGT----RNVVAECLGKLTLIDPETLLP

Caenorhabditis elegans        IWGMLMANAGGNEDGT----RSVVAECLGRLCSFDPESLLP

Drosophila                    IWDQLFKHCECSEEGS----RNVVAECLGKLVLVNPDELLP

Slime mold                    ILPLLFDNCVNEEEGT----RNIVAECLGKLSMIEPNEIIP

Fission yeast                 IWDILSKDIENIKDFSTSPFRTLLSECLGLLICNESSSLYY

Sequence annotation in neighborhood:

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.

Type	Positions	Description
Chain	2 – 1230	Cullin-associated NEDD8-dissociated protein 1
Repeat	928 – 960	HEAT 22
Modified residue	971 – 971	N6-acetyllysine
Alternative sequence	561 – 1230	Missing. In isoform 3.
Helix	947 – 960

Literature citations
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
The MGC Project Team;
Genome Res. 14:2121-2127(2004)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1); VARIANT VAL-952;

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.