UniProtKB/Swiss-Prot Q7L1T6: Variant p.Pro316Ser

Cytochrome b5 reductase 4
Gene: CYB5R4
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Variant information Variant position:

316 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 Proline (P) to Serine (S) at position 316 (P316S, p.Pro316Ser). 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 medium size and hydrophobic (P) to small size and polar (S) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

-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
Polymorphism:

Variants Arg-187 and Arg-223 do not influence the pathogenesis of non-autoimmune diabetes. Additional information on the polymorphism described.
Other resources:

Links to websites of interest for the variant.

Variant rs10080628 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

MLPPSTHLQVPIGQHVYLKL P ITGTEIVKPYTPVSGSLLSE 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                         MLPPSTHLQVPIGQHVYLKLPITGTEIVKPYTPVSGSLLSE

Mouse                         MLPPSTHLQVPVGQHVYLKLSVTGAEIVKPYTPVSDSLLSD

Rat                           MLPPSTHLQVPVGQHVYLKLSVTGAEIVKPYTPVSESLLSD

Bovine                        MLPPSTHLEVPVGQHVYLRLPITGTEIVKPYTPVCDSLFSE

Xenopus tropicalis            QLPQGCHLQVPVGHHIYLKMNISGVDIVKPYTPVASCLLPD

Zebrafish                     QLPRGSRMQVPVGRHVYLKTSVQGTDVVKPYTAVDQMLIPP

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 – 521	Cytochrome b5 reductase 4
Domain	273 – 385	FAD-binding FR-type
Beta strand	310 – 317

Literature citations
Submission
SeattleSNPs variation discovery resource;
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANTS HIS-140; ALA-267 AND SER-316;

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.