UniProtKB/Swiss-Prot Q9UBC5: Variant p.Gly662Glu

Unconventional myosin-Ia
Gene: MYO1A
Feedback?

Variant information Variant position:

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

LB/B 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 Glycine (G) to Glutamate (E) at position 662 (G662E, p.Gly662Glu). 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 glycine (G) to medium size and acidic (E) 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:

Found in a patient with hearing loss; benign. Any additional useful information about the variant.
Other resources:

Links to websites of interest for the variant.

Variant rs33962952 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

1043 The length of the canonical sequence.
Location on the sequence:

SRSTWPHWNGGDREGVEKVL G ELSMSSGELAFGKTKIFIRS 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                         SRSTWPHWNGGDREGVEKVLGELSMSSGELAFGKTKIFIRS

Mouse                         SRSTWPRWNGDDREGVEKVLGSLTLSSEELAYGKTKIFIRS

Bovine                        SRSTWPRWNGGDQEGVEKVLGELSMSSEELAFGKTKIFIRS

Chicken                       SRKTWPRWTGGDREGAEVLLAELKFPPEELAYGHTKIFIRS

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	1 – 1043	Unconventional myosin-Ia
Domain	8 – 694	Myosin motor

Literature citations
Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss.
Donaudy F.; Ferrara A.; Esposito L.; Hertzano R.; Ben-David O.; Bell R.E.; Melchionda S.; Zelante L.; Avraham K.B.; Gasparini P.;
Am. J. Hum. Genet. 72:1571-1577(2003)
Cited for: VARIANTS SER-116 INS; MET-306; ASP-385; GLU-662; ASP-674; PHE-797 AND PRO-910; Targeted and genomewide NGS data disqualify mutations in MYO1A, the 'DFNA48 gene', as a cause of deafness.
Eisenberger T.; Di Donato N.; Baig S.M.; Neuhaus C.; Beyer A.; Decker E.; Muerbe D.; Decker C.; Bergmann C.; Bolz H.J.;
Hum. Mutat. 35:565-570(2014)
Cited for: VARIANT GLU-662; LACK OF INVOLVEMENT IN DFNA48;

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.