UniProtKB/Swiss-Prot P21397: Variant p.Asp15Glu

Amine oxidase [flavin-containing] A
Gene: MAOA
Chromosomal location: Xp11.3-p11.4
Variant information

Variant position:  15
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  Unclassified
The variants are classified into three categories: Disease, Polymorphism and Unclassified.
  • Disease: Variants have been found in patients and disease-association is reported in literature. However, this classification is not a definitive assessment of variant pathogenicity.
  • Polymorphism: No disease-association has been reported.
  • Unclassified: Variants have been found in patients but disease-association remains unclear.

Residue change:  From Aspartate (D) to Glutamate (E) at position 15 (D15E, p.Asp15Glu).
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 acidic.
The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:  2
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 a breast cancer sample; somatic mutation.
Any additional useful information about the variant.



Sequence information

Variant position:  15
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  527
The length of the canonical sequence.

Location on the sequence:   MENQEKASIAGHMF  D VVVIGGGISGLSAAKLLTEY
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                         MENQEKASIAGHMFDVVVIGGGISGLSAAKLLTEY

Mouse                         MTDLEKPSITGHMFDVVVIGGGISGLAAAKLLSEY

Rat                           MTDLEKPNLAGHMFDVGLIGGGISGLAAAKLLSEY

Pig                           MERQEKANNAGHMVDVVVIGGGISGLSAAKLLNEY

Bovine                        MESLQKTSDAGQMFDVVVIGGGISGLSAAKLLAEH

Dog                           MASREKTSIEGHMFDVVVIGGGISGLSAAKLLAEH

Horse                         MASQEKASMAGHMFDVVVIGGGISGLSAAKLLAEH

Slime mold                    ---------MSTLYDVVIVGGGLTGLNAAYQFKKA

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 – 527 Amine oxidase [flavin-containing] A
Topological domain 1 – 497 Cytoplasmic
Modified residue 1 – 1 N-acetylmethionine
Alternative sequence 1 – 133 Missing. In isoform 2.
Beta strand 15 – 19


Literature citations

The consensus coding sequences of human breast and colorectal cancers.
Sjoeblom T.; Jones S.; Wood L.D.; Parsons D.W.; Lin J.; Barber T.D.; Mandelker D.; Leary R.J.; Ptak J.; Silliman N.; Szabo S.; Buckhaults P.; Farrell C.; Meeh P.; Markowitz S.D.; Willis J.; Dawson D.; Willson J.K.V.; Gazdar A.F.; Hartigan J.; Wu L.; Liu C.; Parmigiani G.; Park B.H.; Bachman K.E.; Papadopoulos N.; Vogelstein B.; Kinzler K.W.; Velculescu V.E.;
Science 314:268-274(2006)
Cited for: VARIANT [LARGE SCALE ANALYSIS] GLU-15;

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.