UniProtKB/Swiss-Prot A7XYQ1: Variant p.Ser683Gly

Sine oculis-binding protein homolog
Gene: SOBP
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Variant information Variant position:

683 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant:

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:

From Serine (S) to Glycine (G) at position 683 (S683G, p.Ser683Gly). 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:

Change from small size and polar (S) to glycine (G) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

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:

Links to websites of interest for the variant.

Variant rs9486659 [ dbSNP | Ensembl ]

Sequence information Variant position:

683 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:

873 The length of the canonical sequence.
Location on the sequence:

RLHNVIHRALHAHVKAEREP S AAERRTCGGCRDGHCSPPAA 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:

The multiple alignment of the region surrounding the variant against various orthologous sequences.

Human                         RLHNVIHRALHAHVKAEREP--------SAAERRTCGGCRD---------------GHCSPPAA

Mouse                         RLHNVIHRALHAHVKAEREP--------GAAERRTCGGCRD

Rat                           RLHNVIHRALHAHVKAEREP--------GAAERRTCGGCRD

Bovine                        RLHNVIHRALHAHVKAEREP--------GAAERRTCGGCRD

Chicken                       RLHNVIHRALHAQVKVEREPNSVVNLAFGSSDKRNCSDCRD

Sequence annotation in neighborhood:

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.

Type	Positions	Description
Chain	1 – 873	Sine oculis-binding protein homolog
Modified residue	699 – 699	Phosphoserine
Cross	677 – 677	Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2)

Literature citations
Mutations in Jxc1 cause deafness, vestibular deficits and cochlear malformation in the Jackson circler (jc) mutant mouse.
Chen Z.; Noben-Trauth K.;
Cited for: NUCLEOTIDE SEQUENCE [MRNA]; VARIANT GLY-683;

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.