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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P10275: Variant p.Val867Met

Androgen receptor
Gene: AR
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Variant information Variant position: help 867 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 867 (V867M, p.Val867Met). 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 AIS and prostate cancer. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 867 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 920 The length of the canonical sequence.
Location on the sequence: help RKNPTSCSRRFYQLTKLLDS V QPIARELHQFTFDLLIKSHM 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                         RKNPTSCSRRFYQLTKLLDSVQPIARELHQFTFDLLIKSHM

                              RKNPTSCSRRFYQLTKLLDSVQPIARELHQFTFDLLIKSHM

Rhesus macaque                RKNPTSCSRRFYQLTKLLDSVQPIARELHQFTFDLLIKSHM

Chimpanzee                    RKNPTSCSRRFYQLTKLLDSVQPIARELHQFTFDLLIKSHM

Mouse                         RKNPTSCSRRFYQLTKLLDSVQPIARELHQFTFDLLIKSHM

Rat                           RKNPTSCSRRFYQLTKLLDSVQPIARELHQFTFDLLIKSHM

Pig                           RKNPTSCSRRFYQLTKLLDSVQPIARELHQFTFDLLIKSHM

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 – 920 Androgen receptor
Domain 669 – 900 NR LBD
Region 552 – 919 Interaction with LPXN
Region 592 – 919 Interaction with CCAR1
Region 625 – 919 Interaction with KAT7
Binding site 878 – 878
Cross 848 – 848 Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin)
Alternative sequence 645 – 920 Missing. In isoform 3.
Alternative sequence 649 – 920 Missing. In isoform 4.
Mutagenesis 848 – 848 K -> R. Partially prevents ubiquitination by RNF6.
Helix 850 – 883



Literature citations
Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
Lubahn D.B.; Brown T.R.; Simental J.A.; Higgs H.N.; Migeon C.J.; Wilson E.M.; French F.S.;
Proc. Natl. Acad. Sci. U.S.A. 86:9534-9538(1989)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANT AIS MET-867; Functional characterization of naturally occurring mutant androgen receptors from subjects with complete androgen insensitivity.
Brown T.R.; Lubahn D.B.; Wilson E.M.; French F.S.; Migeon C.J.; Corfen J.L.;
Mol. Endocrinol. 4:1759-1772(1990)
Cited for: VARIANTS AIS CYS-775; GLN-832 AND MET-867; Substitution of valine-865 by methionine or leucine in the human androgen receptor causes complete or partial androgen insensitivity, respectively with distinct androgen receptor phenotypes.
Kazemi-Esfarjani P.; Beitel L.K.; Trifiro M.A.; Kaufman M.; Rennie P.; Sheppard P.; Matusik R.; Pinsky L.;
Mol. Endocrinol. 7:37-46(1993)
Cited for: VARIANT AIS MET-867; VARIANT PAIS LEU-867; Clinical and biochemical investigations and molecular analysis of subjects with mutations in the androgen receptor gene.
Weidemann W.; Linck B.; Haupt H.; Mentrup B.; Romalo G.; Stockklauser K.; Brinkmann A.O.; Schweikert H.-U.; Spindler K.D.;
Clin. Endocrinol. (Oxf.) 45:733-739(1996)
Cited for: VARIANTS PAIS GLN-608; THR-611; LEU-755; HIS-841; THR-843 AND HIS-856; VARIANT AIS MET-867;
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.