UniProtKB/Swiss-Prot P13569: Variant p.Arg31Cys

Cystic fibrosis transmembrane conductance regulator
Gene: CFTR
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Variant information Variant position:

31 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 31 (R31C, p.Arg31Cys). 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
Other resources:

Links to websites of interest for the variant.

Variant rs1800073 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

1480 The length of the canonical sequence.
Location on the sequence:

VVSKLFFSWTRPILRKGYRQ R LELSDIYQIPSVDSADNLSE 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                         VVSKLFFSWTRPILRKGYRQRLELSDIYQIPSVDSADNLSE

Gorilla                       VVSKLFFSWTRPILRKGYRQRLELSDIYQIPSVDSADNLSE

                              VLSKLFFSWTRPILIKGYRQRLELSDIYQVPSTDSADHLSE

Rhesus macaque                VVSKLFFSWTRPILRKGYRQRLELSDIYQIPSADSADNLSE

Chimpanzee                    VVSKLFFSWTRPILRKGYRQRLELSDIYQIPSVDSADNLSE

Mouse                         FISKLFFSWTTPILRKGYRHHLELSDIYQAPSADSADHLSE

Rat                           FISKLFFSWTTPILRKGYRHHLELSDIYQAPSSDSADHLSE

Pig                           IFSKLFFSWTRPILRKGYRQRLELSDIYHISSSDSADNLSE

Bovine                        VVSKLFFSWTRPILKKGYRQRLELSDIYHISSSDSADNLSE

Rabbit                        VLSKLFFSWTRPILRKGYRQRLELSDIYQIPSADSADNLSE

Sheep                         VVSKLFFSWTRPILKKGYRQRLELSDIYHISSSDSADNLSE

Horse                         VISKLFFSWTRPILRKGYRQRLELSDIYQIPSADSADNLSE

Xenopus laevis                IFSQIFFSWTKPILWKGYRQRLELSDIYQIHPGDSADNLSE

Zebrafish                     CLSRYFFWWTNPIMRKGFKEKLRPSDVYQAPSQDAADILAE

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 – 1480	Cystic fibrosis transmembrane conductance regulator
Topological domain	1 – 77	Cytoplasmic

Literature citations
Identification of eight mutations and three sequence variations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
Ghanem N.; Costes B.; Girodon E.; Martin J.; Fanen P.; Goossens M.;
Genomics 21:434-436(1994)
Cited for: VARIANTS CYS-31 AND ILE-1220; VARIANTS CF 890-GLN--LEU-1480 DEL; LEU-912; TYR-949; PRO-1065; PRO-1071 AND 1204-TRP--LEU-1480 DEL; Complete mutational screening of the CFTR gene in 120 patients with pulmonary disease.
Bombieri C.; Benetazzo M.; Saccomani A.; Belpinati F.; Gile L.S.; Luisetti M.; Pignatti P.F.;
Hum. Genet. 103:718-722(1998)
Cited for: VARIANTS CYS-31; GLN-75; VAL-506 AND CYS-668; VARIANTS CF CYS-301; ASN-651; MET-754 AND LEU-1072;

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.