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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q14654: Variant p.Leu270Val

ATP-sensitive inward rectifier potassium channel 11
Gene: KCNJ11
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Variant information Variant position: help 270 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help 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: help From Leucine (L) to Valine (V) at position 270 (L270V, p.Leu270Val). 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 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: 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

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


Sequence information Variant position: help 270 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 390 The length of the canonical sequence.
Location on the sequence: help FLVAPLIIYHVIDANSPLYD L APSDLHHHQDLEIIVILEGV 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                         FLVAPLIIYHVIDANSPLYDLAPSDLHHHQDLEIIVILEGV

Mouse                         FLVAPLIIYHVIDSNSPLYDLAPSDLHHHQDLEIIVILEGV

Rat                           FLVAPLIIYHVIDSNSPLYDLAPSDLHHHQDLEIIVILEGV

Rabbit                        FLVAPLIIHHVIDANSPLYDLAPSDLHHHQDLEIIVILEGV

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 – 390 ATP-sensitive inward rectifier potassium channel 11
Topological domain 167 – 390 Cytoplasmic



Literature citations
Sequence variations in the human Kir6.2 gene, a subunit of the beta-cell ATP-sensitive K-channel: no association with NIDDM in white Caucasian subjects or evidence of abnormal function when expressed in vitro.
Sakura H.; Wat N.; Horton V.; Millns H.; Turner R.C.; Ashcroft F.M.;
Diabetologia 39:1233-1236(1996)
Cited for: VARIANTS NIDDM PRO-355 AND LYS-PRO-380 INS; VARIANTS GLU-23; VAL-270; ILE-337 AND CYS-385; Sequence variants in the pancreatic islet beta-cell inwardly rectifying K+ channel Kir6.2 (Bir) gene: identification and lack of role in Caucasian patients with NIDDM.
Inoue H.; Ferrer J.; Warren-Perry M.; Zhang Y.; Millns H.; Turner R.C.; Elbein S.C.; Hampe C.L.; Suarez B.K.; Inagaki N.; Seino S.; Permutt M.A.;
Diabetes 46:502-507(1997)
Cited for: VARIANTS LYS-10; GLU-23; VAL-270 AND ILE-337;
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.