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UniProtKB/Swiss-Prot P16615: Variant p.Asn101Ser

Sarcoplasmic/endoplasmic reticulum calcium ATPase 2
Gene: ATP2A2
Variant information

Variant position:  101
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 Asparagine (N) to Serine (S) at position 101 (N101S, p.Asn101Ser).
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 (N) to small size and polar (S)
The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:  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:  In DD.
Any additional useful information about the variant.



Sequence information

Variant position:  101
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  1042
The length of the canonical sequence.

Location on the sequence:   GEETITAFVEPFVILLILVA  N AIVGVWQERNAENAIEALKE
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                         GEETITAFVEPFVILLILVANAIVGVWQERNAENAIEALKE

                              GEETITAFVEPFVILLILVANAIVGVWQERNAENAIEALKE

Mouse                         GEETITAFVEPFVILLILVANAIVGVWQERNAENAIEALKE

Rat                           GEETITAFVEPFVILLILVANAIVGVWQERNAENAIEALKE

Pig                           GEETITAFVEPFVILLILVANAIVGVWQERNAENAIEALKE

Rabbit                        GEETITAFVEPFVILLILVANAIVGVWQERNAENAIEALKE

Cat                           GEETITAFVEPFVILLILVANAIVGVWQERNAENAIEALKE

Chicken                       GEETITAFVEPFVILLILVANAIVGVWQERNAENAIEALKE

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 1 – 1042 Sarcoplasmic/endoplasmic reticulum calcium ATPase 2
Transmembrane 90 – 110 Helical; Name=2
Helix 89 – 116


Literature citations

Mendelian Disorders of Cornification Caused by Defects in Intracellular Calcium Pumps: Mutation Update and Database for Variants in ATP2A2 and ATP2C1 associated with Darier disease and Hailey-Hailey disease.
Nellen R.G.; Steijlen P.M.; van Steensel M.A.; Vreeburg M.; Frank J.; van Geel M.;
Hum. Mutat. 38:343-356(2017)
Cited for: VARIANTS DD 74-VAL--GLN-108 DEL; SER-101; GLN-131; 194-VAL--PRO-197 DEL; PRO-590; ALA-625; GLU-626; 666-ARG--SER-1042 DEL; PRO-672; PRO-691; TRP-750; TRP-765; GLY-849 INS; PRO-900 AND ARG-943;

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.