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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9H2C2: Variant p.Gly189Arg

Protein ARV1
Gene: ARV1
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Variant information Variant position: help 189 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] 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 Glycine (G) to Arginine (R) at position 189 (G189R, p.Gly189Arg). 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 glycine (G) to large size and basic (R) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -2 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 DEE38; loss of protein stability; yeast complementation assays show that the variant does partially rescue cell growth. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 189 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 271 The length of the canonical sequence.
Location on the sequence: help TAKKKPNFILLLKALLLSSY G KLLLIPAVIWEHDYTSVCLK 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                         TAKKKPNFILLLKALLLSSYGKLLLIPAVIWEHDYTSVCLK

Mouse                         TAKRAPDFVLLLKALLLSSYGKLLLIPAVIWEHDYTPLCLR

Bovine                        RAKEKLNFTLLLKALLLSSYGKLLLIPAVIWEHDYTPLCLR

Slime mold                    ---PIIKYNYLIMAIILSSFGKGFLVLMMIWDYPFSFGS--

Baker's yeast                 SSKDVISYT-----ILLSYGAKIFPILMLIWPYD-TLISMS

Fission yeast                 ASGAVI----------LSSSTRMLPVFMVIWDYDLSIAA-T
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 – 271 Protein ARV1
Transmembrane 176 – 196 Helical



Literature citations
Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families.
Alazami A.M.; Patel N.; Shamseldin H.E.; Anazi S.; Al-Dosari M.S.; Alzahrani F.; Hijazi H.; Alshammari M.; Aldahmesh M.A.; Salih M.A.; Faqeih E.; Alhashem A.; Bashiri F.A.; Al-Owain M.; Kentab A.Y.; Sogaty S.; Al Tala S.; Temsah M.H.; Tulbah M.; Aljelaify R.F.; Alshahwan S.A.; Seidahmed M.Z.; Alhadid A.A.; Aldhalaan H.; Alqallaf F.; Kurdi W.; Alfadhel M.; Babay Z.; Alsogheer M.; Kaya N.; Al-Hassnan Z.N.; Abdel-Salam G.M.; Al-Sannaa N.; Al Mutairi F.; El Khashab H.Y.; Bohlega S.; Jia X.; Nguyen H.C.; Hammami R.; Adly N.; Mohamed J.Y.; Abdulwahab F.; Ibrahim N.; Naim E.A.; Al-Younes B.; Meyer B.F.; Hashem M.; Shaheen R.; Xiong Y.; Abouelhoda M.; Aldeeri A.A.; Monies D.M.; Alkuraya F.S.;
Cell Rep. 10:148-161(2015)
Cited for: VARIANT DEE38 ARG-189; INVOLVEMENT IN DEE38; Neuronal deficiency of ARV1 causes an autosomal recessive epileptic encephalopathy.
Palmer E.E.; Jarrett K.E.; Sachdev R.K.; Al Zahrani F.; Hashem M.O.; Ibrahim N.; Sampaio H.; Kandula T.; Macintosh R.; Gupta R.; Conlon D.M.; Billheimer J.T.; Rader D.J.; Funato K.; Walkey C.J.; Lee C.S.; Loo C.; Brammah S.; Elakis G.; Zhu Y.; Buckley M.; Kirk E.P.; Bye A.; Alkuraya F.S.; Roscioli T.; Lagor W.R.;
Hum. Mol. Genet. 25:3042-3054(2016)
Cited for: VARIANTS DEE38 59-LYS--ASN-98 DEL AND ARG-189; CHARACTERIZATION OF VARIANTS DEE38 59-LYS--ASN-98 AND ARG-189;
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.