UniProtKB/Swiss-Prot A1E959: Variant p.Glu269Asp

Odontogenic ameloblast-associated protein
Gene: ODAM
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Variant information Variant position:

269 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant:

US 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 Glutamate (E) to Aspartate (D) at position 269 (E269D, p.Glu269Asp). 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 colorectal cancer sample; somatic mutation. Any additional useful information about the variant.

Sequence information Variant position:

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

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

STTNVFTSAVDQTITPELPE E KDKTDSLREP 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                         STTNVFTSAVDQTITPELPEEKDKTDSLREP

                              STTNYFAPAIDPTITPELMEKKAKTDYLKEP

Rhesus macaque                STTNVFTSAIDRTITAKFPEEKAKTDGLREP

Chimpanzee                    STTNAFTSAVDQTITPELPEEKDKTDSLREP

Mouse                         STDNFFTSGIDPTIAP---EQKVKTDSLREP

Rat                           DTGNFFTSEINPTIAPLLPEQKVNADSLREP

Pig                           STTNVFTSTVDPTITPKVMEKKAKTDSLKEP

Bovine                        STTIFFTSAVDPIITRELTEKKAKTDSLKEP

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	16 – 279	Odontogenic ameloblast-associated protein
Region	243 – 279	Disordered
Compositional bias	264 – 279	Basic and acidic residues
Glycosylation	249 – 249	O-linked (GalNAc...) serine
Glycosylation	250 – 250	O-linked (GalNAc...) threonine
Glycosylation	251 – 251	O-linked (GalNAc...) threonine
Glycosylation	255 – 255	O-linked (GalNAc...) threonine
Glycosylation	256 – 256	O-linked (GalNAc...) serine
Glycosylation	261 – 261	O-linked (GalNAc...) threonine
Glycosylation	263 – 263	O-linked (GalNAc...) threonine
Glycosylation	273 – 273	O-linked (GalNAc...) threonine
Glycosylation	275 – 275	O-linked (GalNAc...) serine

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] ASP-269;

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.