UniProtKB/Swiss-Prot O43543: Variant p.Ile95Val

DNA repair protein XRCC2
Gene: XRCC2
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Variant information Variant position:

95 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 Isoleucine (I) to Valine (V) at position 95 (I95V, p.Ile95Val). 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:

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:

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
Variant description:

Does not affect function in double-strand break repair via homologous recombination as shown in rescue assays of XRCC2-deficient cells. Any additional useful information about the variant.
Other resources:

Links to websites of interest for the variant.

Variant rs140214637 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

EVEVLFIDTDYHFDMLRLVT I LEHRLSQSSEEIIKYCLGRF 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                         EVEVLFIDTDYHFDMLRLVTILEHRLSQSSEEIIKYCLGRF

Mouse                         QIEVLFIDTDYHFDMLRLVTVLEHRLSQSSEEAMKLCLARL

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 – 280	DNA repair protein XRCC2
Helix	89 – 99

Literature citations
Rare mutations in XRCC2 increase the risk of breast cancer.
Park D.J.; Lesueur F.; Nguyen-Dumont T.; Pertesi M.; Odefrey F.; Hammet F.; Neuhausen S.L.; John E.M.; Andrulis I.L.; Terry M.B.; Daly M.; Buys S.; Le Calvez-Kelm F.; Lonie A.; Pope B.J.; Tsimiklis H.; Voegele C.; Hilbers F.M.; Hoogerbrugge N.; Barroso A.; Osorio A.; Giles G.G.; Devilee P.; Benitez J.; Hopper J.L.; Tavtigian S.V.; Goldgar D.E.; Southey M.C.;
Am. J. Hum. Genet. 90:734-739(2012)
Cited for: VARIANTS SER-16; ILE-61; TRP-91; VAL-95; CYS-231 AND VAL-270; Rare variants in XRCC2 as breast cancer susceptibility alleles.
Hilbers F.S.; Wijnen J.T.; Hoogerbrugge N.; Oosterwijk J.C.; Collee M.J.; Peterlongo P.; Radice P.; Manoukian S.; Feroce I.; Capra F.; Couch F.J.; Wang X.; Guidugli L.; Offit K.; Shah S.; Campbell I.G.; Thompson E.R.; James P.A.; Trainer A.H.; Gracia J.; Benitez J.; van Asperen C.J.; Devilee P.;
J. Med. Genet. 49:618-620(2012)
Cited for: VARIANTS ARG-47; GLN-75; VAL-95; ALA-118; TYR-120; PRO-133; GLN-164; ALA-170; CYS-188; MET-194; LEU-199; GLY-207; VAL-220; SER-238; GLU-248; CYS-258 AND VAL-270; Functional analysis of missense variants in the putative breast cancer susceptibility gene XRCC2.
Hilbers F.S.; Luijsterburg M.S.; Wiegant W.W.; Meijers C.M.; Voelker-Albert M.; Boonen R.A.; van Asperen C.J.; Devilee P.; van Attikum H.;
Hum. Mutat. 37:914-925(2016)
Cited for: VARIANTS SER-16; ARG-47; ILE-61; GLN-75; TRP-91; VAL-95; ALA-118; TYR-120; PRO-133; GLN-164; ALA-170; CYS-188; HIS-188; MET-194; LEU-199; GLY-207; VAL-220; CYS-231; SER-238; GLU-248; CYS-258 AND VAL-270; FUNCTION; CHARACTERIZATION OF VARIANTS SER-16; ARG-47; ILE-61; GLN-75; TRP-91; VAL-95; ALA-118; TYR-120; PRO-133; GLN-164; ALA-170; CYS-188; HIS-188; MET-194; LEU-199; GLY-207; VAL-220; CYS-231; SER-238; GLU-248; CYS-258 AND VAL-270;

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.