UniProtKB/Swiss-Prot P02765: Variant p.Arg317Cys

Alpha-2-HS-glycoprotein
Gene: AHSG
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Variant information Variant position:

317 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 Arginine (R) to Cysteine (C) at position 317 (R317C, p.Arg317Cys). 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 large size and basic (R) to medium size and polar (C) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

-3 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:

There are two common alleles, AHSG*1 and AHSG*2. AHSG*1 has Thr-248/Thr-256; AHSG*2 has Met-248/Ser-256. Additional information on the polymorphism described.
Variant description:

In allele AHSG*3. Any additional useful information about the variant.
Other resources:

Links to websites of interest for the variant.

Variant rs35457250 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

SHVLLAAPPGHQLHRAHYDL R HTFMGVVSLGSPSGEVSHPR 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                         SHVLLAAPPGHQLHRAHYDLRHTFMGVVSLGSPSGEVSHPR

Chimpanzee                    SHVLLAAPPGHQLHWAHYDLRHTFMGVVSLGSPSGEASHPR

Mouse                         ----VVVPRGLSDHRTYHDLRHAFSPVASVESASGETLH--

Rat                           ----VAVPLGLPDHRTHHDLRHAFSPVASVESASGEVLH--

Bovine                        ---VVAVP--LPLHRAHYDLRHTFSGVASVESSSGEAFHVG

Sheep                         ---VVAVP--LPLHRAHYDLRHTFSGVASVESASGEAFHVG

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
Propeptide	301 – 340	Connecting peptide
Modified residue	319 – 319	Phosphothreonine; by FAM20C
Modified residue	325 – 325	Phosphoserine; by FAM20C
Modified residue	328 – 328	Phosphoserine; by FAM20C
Modified residue	330 – 330	Phosphoserine; by FAM20C
Disulfide bond	32 – 358	Interchain (between A and B chains)

Literature citations
Haplotype analysis of the human alpha2-HS glycoprotein (fetuin) gene.
Osawa M.; Yuasa I.; Kitano T.; Henke J.; Kaneko M.; Udono T.; Saitou N.; Umetsu K.;
Ann. Hum. Genet. 65:27-34(2001)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANTS THR-248; THR-256; ASN-276 AND CYS-317;

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.