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UniProtKB/Swiss-Prot P00746: Variant p.Cys214Arg

Complement factor D
Gene: CFD
Variant information

Variant position:  214
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  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:  From Cysteine (C) to Arginine (R) at position 214 (C214R, p.Cys214Arg).
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 polar (C) to large size and basic (R)
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:  In CFDD.
Any additional useful information about the variant.

Other resources:  
Links to websites of interest for the variant.



Sequence information

Variant position:  214
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  253
The length of the canonical sequence.

Location on the sequence:   MCAESNRRDSCKGDSGGPLV  C GGVLEGVVTSGSRVCGNRKK
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                         MCAESNRRDSCKGDSGGPLVCGGV----------------------------LEGVVTSGSRVCGNRKK

Mouse                         MCAESNRRDTCRGDSGSPLVCGDA-----------------

Rat                           MCAESNRRDTCRGDSGGPLVCGDA-----------------

Pig                           MCAESNRRDSCKGDSGGPLVCGGV-----------------

Bovine                        MCAESNRRDTCKGDSGGPLVCGSV-----------------

Slime mold                    PSTVDWRNQNCVTPVKDQGICGSCWTFGSTGSLEGTNCVTN

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.

TypePositionsDescription
Chain 26 – 253 Complement factor D
Domain 26 – 253 Peptidase S1
Active site 208 – 208 Charge relay system
Disulfide bond 148 – 214
Disulfide bond 204 – 229
Beta strand 211 – 214


Literature citations

Deficient alternative complement pathway activation due to factor D deficiency by 2 novel mutations in the complement factor D gene in a family with meningococcal infections.
Sprong T.; Roos D.; Weemaes C.; Neeleman C.; Geesing C.L.; Mollnes T.E.; van Deuren M.;
Blood 107:4865-4870(2006)
Cited for: VARIANTS CFDD DEFICIENCY GLY-213 AND ARG-214;

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.