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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q96S37: Variant p.Val388Met

Solute carrier family 22 member 12
Gene: SLC22A12
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Variant information Variant position: help 388 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help US 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 Valine (V) to Methionine (M) at position 388 (V388M, p.Val388Met). 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

Variant description: help In RHUC1; uncertain significance; no effect on urate transport; no effect on its localization to cell membrane. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 388 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 553 The length of the canonical sequence.
Location on the sequence: help ALDLQALGSNIFLLQMFIGV V DIPAKMGALLLLSHLGRRPT 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                         ALDLQALGSNIFLLQMFIGVVDIPAKMGALLLLSHLGRRPT

Mouse                         ALDLQALGSNIFLLQALIGIVDFPVKTGSLLLISRLGRRFC

Rat                           ALDLQALGSNIFLLQALIGIVDLPVKMGSLLLLSRLGRRLC

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 – 553 Solute carrier family 22 member 12
Transmembrane 378 – 398 Helical



Literature citations
Clinical and functional characterization of URAT1 variants.
Tasic V.; Hynes A.M.; Kitamura K.; Cheong H.I.; Lozanovski V.J.; Gucev Z.; Jutabha P.; Anzai N.; Sayer J.A.;
PLoS ONE 6:e28641-e28641(2011)
Cited for: VARIANTS RHUC1 THR-75; SER-347; MET-388; CYS-434 AND HIS-434; CHARACTERIZATION OF VARIANTS RHUC1 THR-75; SER-347; MET-388; CYS-434 AND HIS-434; FUNCTION; SUBCELLULAR LOCATION;
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.