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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P13569: Variant p.Gly622Asp

Cystic fibrosis transmembrane conductance regulator
Gene: CFTR
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Variant information Variant position: help 622 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] 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: help From Glycine (G) to Aspartate (D) at position 622 (G622D, p.Gly622Asp). 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: help Change from glycine (G) to medium size and acidic (D) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -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
Variant description: help In CBAVD; decreased channel activity; has no effect on glycan maturation. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 622 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 1480 The length of the canonical sequence.
Location on the sequence: help LVTSKMEHLKKADKILILHE G SSYFYGTFSELQNLQPDFSS 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: help The multiple alignment of the region surrounding the variant against various orthologous sequences. 
Human                         LVTSKMEHLKKADKILILHEGSSYFYGTFSELQNLQPDFSS

Gorilla                       LVTSKMEHLKKADKILILHEGSSYFYGTFSELQNLRPDFSS

                              LVTSKMEHLKKADKVLILHEGSCYFYGTFSELQSLRPDFSS

Rhesus macaque                LVTSKMEHLKKADKILILHEGSSYFYGTFSELQNLRPDFSS

Chimpanzee                    LVTSKMEHLKKADKILILHEGSSYFYGTFSELQNLRPDFSS

Mouse                         LVTSKMEHLRKADKILILHQGSSYFYGTFSELQSLRPDFSS

Rat                           LVTSKMEQLKKADKILILHEGSSYFYGTFSELQSLRPDFSS

Pig                           LVTSKMEHLKKADKILILHEGSSYFYGTFSELQSQRPDFSS

Bovine                        LVTSKMEHLKKADKILILHEGSIYFYGTFSELQNQRPDFSS

Rabbit                        LVTSKMEHLKKADKILILHEGSSYFYGTFSELQSLRPDFSS

Sheep                         LVTSKMEHLKKADKILILHEGSVYFYGTFSELQNQRPDFSS

Horse                         LVTSKMEHLKKADKILILHEGSSYFYGTFSELQNLRPDFSS

Xenopus laevis                LVTSKVEQLKKADKVLILHEGSCYFYGTFSELEDQRPEFSS

Zebrafish                     LVTNKIEHLKRADKILLLHNGESFFYGTFPELQSERPDFSS
Sequence annotation in neighborhood: help 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.
TypePositionsDescription
Chain 1 – 1480 Cystic fibrosis transmembrane conductance regulator
Topological domain 359 – 858 Cytoplasmic
Domain 423 – 646 ABC transporter 1
Alternative sequence 606 – 1480 Missing. In isoform 3.



Literature citations
Characterization of 19 disease-associated missense mutations in the regulatory domain of the cystic fibrosis transmembrane conductance regulator.
Vankeerberghen A.; Wei L.; Jaspers M.; Cassiman J.-J.; Nilius B.; Cuppens H.;
Hum. Mol. Genet. 7:1761-1769(1998)
Cited for: CHARACTERIZATION OF VARIANTS CF PHE-601; SER-610; THR-613; GLY-614; THR-618; SER-619; GLN-620; PRO-620; ARG-628; PRO-633; SER-665; LEU-693 AND LYS-822; CHARACTERIZATION OF VARIANTS CBAVD ASP-622; MET-766; GLY-792; GLY-800 AND MET-807; CHARACTERIZATION OF VARIANT THORACIC SARCOIDOSIS LYS-826; Detection of cystic fibrosis transmembrane conductance regulator (CFTR) gene rearrangements enriches the mutation spectrum in congenital bilateral absence of the vas deferens and impacts on genetic counselling.
Ratbi I.; Legendre M.; Niel F.; Martin J.; Soufir J.C.; Izard V.; Costes B.; Costa C.; Goossens M.; Girodon E.;
Hum. Reprod. 22:1285-1291(2007)
Cited for: VARIANTS GLN-75 AND MET-470; VARIANTS CBAVD TRP-74; HIS-110; HIS-117; HIS-170; TRP-206; ASP-232; TRP-334; TYR-443; PHE-508 DEL; VAL-556; ILE-562; ALA-576; ASP-622; CYS-668; GLY-938; ILE-952; VAL-959; PHE-977; PHE-997; CYS-1032; ARG-1069; HIS-1152; GLU-1153; ASN-1270; 1282-TRP--LEU-1480 DEL; HIS-1352 AND 1473-GLU--LEU-1480 DEL;
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.