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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9HC96: Variant p.Arg202His

Calpain-10
Gene: CAPN10
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Variant information Variant position: help 202 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 Arginine (R) to Histidine (H) at position 202 (R202H, p.Arg202His). 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 medium size and polar (H) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help 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: help Links to websites of interest for the variant.


Sequence information Variant position: help 202 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 672 The length of the canonical sequence.
Location on the sequence: help AERWNLKGVAGSGGQQDRPG R WEHRTCRQLLHLKDQCLISC 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                         AERWNLKGVAGSGGQQDRPGRWEHRTCRQLLHLKDQCLISC

Mouse                         AERWSLKDVTKASGQQDRPSGGEHRTCRQLLHLKDRCLISC

Rat                           AERWSLKDIRKASGQQDRPSGGEHRACQQLLRLKDQCLLSC

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 – 672 Calpain-10
Domain 13 – 321 Calpain catalytic
Alternative sequence 48 – 581 Missing. In isoform H.
Alternative sequence 140 – 672 Missing. In isoform G.
Alternative sequence 154 – 274 VYAKVHGSYEHLWAGQVADALVDLTGGLAERWNLKGVAGSGGQQDRPGRWEHRTCRQLLHLKDQCLISCCVLSPRAGARELGEFHAFIVSDLRELQGQAGQCILLLRIQNPWGRRCWQGLW -> GPWVLRAPVGRAGGGCPGGPDRRPGRKMEPEGRSRKRRPAGQARPLGAQDLSAAAPPEGPVSDQLLRAQPQSRCPGAGGVPCLHCLGPAGAPGSGGPVHPAAADPEPLGPAVLAGALERGG. In isoform F.



Literature citations
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.
Horikawa Y.; Oda N.; Cox N.J.; Li X.; Orho-Melander M.; Hara M.; Hinokio Y.; Lindner T.H.; Mashima H.; Schwarz P.E.H.; del Bosque-Plata L.; Horikawa Y.; Oda Y.; Yoshiuchi I.; Colilla S.; Polonsky K.S.; Wei S.; Concannon P.; Iwasaki N.; Schulze J.; Baier L.J.; Bogardus C.; Groop L.; Boerwinkle E.; Hanis C.L.; Bell G.I.;
Nat. Genet. 26:163-175(2000)
Cited for: NUCLEOTIDE SEQUENCE [MRNA]; ALTERNATIVE SPLICING; VARIANTS THR-200; HIS-202; VAL-341; ALA-504; SER-529; ASN-613 AND VAL-666; INVOLVEMENT IN SUSCEPTIBILITY TO T2D1;
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.