UniProtKB/Swiss-Prot Q96GX5: Variant p.Pro620Ala

Serine/threonine-protein kinase greatwall
Gene: MASTL
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Variant information Variant position:

620 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 Proline (P) to Alanine (A) at position 620 (P620A, p.Pro620Ala). 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 hydrophobic (P) to small size and hydrophobic (A) 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
Other resources:

Links to websites of interest for the variant.

Variant rs3802526 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

EESNIEDPLIVTPDCQEKTS P KGVENPAVQESNQKMLGPPL 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                         EESNIEDPLIVTPDCQEKT----------SPKGVENPAVQ----------------ESNQKMLGPPL

                              EESNIEDLLAVSPSWQENP----------LPKDDENLAVQ-

Mouse                         EEPNTEDLFVL-PKCQENS----------LPQDDCHACIQ-

Bovine                        EESNIEDLLPVSPSCQEST----------LPKGVECPTIQ-

Chicken                       EEPKAEDLLTMSPNCQEAS-----------RNGVEADVVQN

Xenopus laevis                EESQSENSEEITPDNKGIPFMAENDERVQSKYEPNTSILP-

Xenopus tropicalis            EESPSESNEETTPENKGMAFMAENDA---LKREPNRSVLP-

Zebrafish                     EELDENEISAVTPMARPTV-ATPKHSSAKQRRGECERSLL-

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 – 879	Serine/threonine-protein kinase greatwall
Domain	35 – 835	Protein kinase
Region	566 – 632	Disordered
Modified residue	631 – 631	Phosphoserine

Literature citations
Patterns of somatic mutation in human cancer genomes.
Greenman C.; Stephens P.; Smith R.; Dalgliesh G.L.; Hunter C.; Bignell G.; Davies H.; Teague J.; Butler A.; Stevens C.; Edkins S.; O'Meara S.; Vastrik I.; Schmidt E.E.; Avis T.; Barthorpe S.; Bhamra G.; Buck G.; Choudhury B.; Clements J.; Cole J.; Dicks E.; Forbes S.; Gray K.; Halliday K.; Harrison R.; Hills K.; Hinton J.; Jenkinson A.; Jones D.; Menzies A.; Mironenko T.; Perry J.; Raine K.; Richardson D.; Shepherd R.; Small A.; Tofts C.; Varian J.; Webb T.; West S.; Widaa S.; Yates A.; Cahill D.P.; Louis D.N.; Goldstraw P.; Nicholson A.G.; Brasseur F.; Looijenga L.; Weber B.L.; Chiew Y.-E.; DeFazio A.; Greaves M.F.; Green A.R.; Campbell P.; Birney E.; Easton D.F.; Chenevix-Trench G.; Tan M.-H.; Khoo S.K.; Teh B.T.; Yuen S.T.; Leung S.Y.; Wooster R.; Futreal P.A.; Stratton M.R.;
Nature 446:153-158(2007)
Cited for: VARIANTS [LARGE SCALE ANALYSIS] LYS-337; ILE-610 AND ALA-620;

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.