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UniProtKB/Swiss-Prot O95477: Variant p.Val2244Ile

Phospholipid-transporting ATPase ABCA1
Gene: ABCA1
Variant information

Variant position:  2244
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  Polymorphism
The variants are classified into three categories: Disease, Polymorphism and Unclassified.
  • Disease: Variants implicated in disease according to literature reports.
  • Polymorphism: Variants not reported to be implicated in disease.
  • Unclassified: Variants with uncertain implication in disease according to literature reports. Evidence against or in favor of a pathogenic role is limited and/or conflicting.

Residue change:  From Valine (V) to Isoleucine (I) at position 2244 (V2244I, p.Val2244Ile).
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:  Similar physico-chemical property. Both residues are medium size and hydrophobic.
The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:  3
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

Polymorphism:  Genetic variations in ABCA1 define the high density lipoprotein cholesterol level quantitative trait locus 13 (HDLCQ13) [MIM:600046].
Additional information on the polymorphism described.

Variant description:  Could be associated with reduced plasma HDL cholesterol.
Any additional useful information about the variant.

Other resources:  
Links to websites of interest for the variant.



Sequence information

Variant position:  2244
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  2261
The length of the canonical sequence.

Location on the sequence:   QSDDDHLKDLSLHKNQTVVD  V AVLTSFLQDEKVKESYV
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                         QSDDDHLKDLSLHKNQTVVDVAVLTSFLQDEKVKESYV

Mouse                         QSDDDHLKDLSLHKNQTVVDVAVLTSFLQDEKVKESYV

Slime mold                    -----HLAKLKTQ-------------------------

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.

TypePositionsDescription
Chain 1 – 2261 Phospholipid-transporting ATPase ABCA1
Glycosylation 2238 – 2238 N-linked (GlcNAc...) asparagine


Literature citations

Screening for functional sequence variations and mutations in ABCA1.
Probst M.C.; Thumann H.; Aslanidis C.; Langmann T.; Buechler C.; Patsch W.; Baralle F.E.; Dallinga-Thie G.M.; Geisel J.; Keller C.; Menys V.C.; Schmitz G.;
Atherosclerosis 175:269-279(2004)
Cited for: VARIANTS HDLD1 LEU-590; ARG-840 AND CYS-1068; VARIANTS MET-771; SER-2163 AND ILE-2244;

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.