UniProtKB/Swiss-Prot Q9NYP3: Variant p.Ser28Arg

Protein downstream neighbor of Son
Gene: DONSON
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Variant information Variant position:

28 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 Serine (S) to Arginine (R) at position 28 (S28R, p.Ser28Arg). 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 small size and polar (S) to large size and basic (R) 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:

No effect on nuclear localization; complements loss of endogenous DONSON by rescuing the spontaneous fork stalling observed after DONSON depletion. Any additional useful information about the variant.
Other resources:

Links to websites of interest for the variant.

Variant rs768071555 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

YSPGFRKPPEVVRLRRKRAR S RGAAASPPRELTEPAARRAA 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                         YSPGFRKPPEVVRLRRKRARSRGAAASPPRELTEPAARRAA

Mouse                         YSPSFKRPPETVRLRRKRSRDHGAA--VPASLPEPAPRRAA

Xenopus laevis                YSPSFKKPSEILRLSRRRSRSEASKTGLSPFSPGDVIKRVP

Xenopus tropicalis            YSPSFKKPSEILRLSRRRSRSEASKAGVSPFSPGDVTKRVP

Drosophila                    VASKWTRPDDFIKLQRLKQKKNKLAARVSNNNNRRPRHQVD

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 – 566	Protein downstream neighbor of Son
Region	1 – 110	Disordered
Modified residue	28 – 28	Phosphoserine
Modified residue	34 – 34	Phosphoserine

Literature citations
Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism.
Reynolds J.J.; Bicknell L.S.; Carroll P.; Higgs M.R.; Shaheen R.; Murray J.E.; Papadopoulos D.K.; Leitch A.; Murina O.; Tarnauskaite Z.; Wessel S.R.; Zlatanou A.; Vernet A.; von Kriegsheim A.; Mottram R.M.; Logan C.V.; Bye H.; Li Y.; Brean A.; Maddirevula S.; Challis R.C.; Skouloudaki K.; Almoisheer A.; Alsaif H.S.; Amar A.; Prescott N.J.; Bober M.B.; Duker A.; Faqeih E.; Seidahmed M.Z.; Al Tala S.; Alswaid A.; Ahmed S.; Al-Aama J.Y.; Altmueller J.; Al Balwi M.; Brady A.F.; Chessa L.; Cox H.; Fischetto R.; Heller R.; Henderson B.D.; Hobson E.; Nuernberg P.; Percin E.F.; Peron A.; Spaccini L.; Quigley A.J.; Thakur S.; Wise C.A.; Yoon G.; Alnemer M.; Tomancak P.; Yigit G.; Taylor A.M.; Reijns M.A.; Simpson M.A.; Cortez D.; Alkuraya F.S.; Mathew C.G.; Jackson A.P.; Stewart G.S.;
Nat. Genet. 49:537-549(2017)
Cited for: INVOLVEMENT IN MISSLA; VARIANTS MISSLA ARG-278; CYS-282; LEU-292; 293-ARG--SER-566 DEL; 417-ASN-SER-418 DEL; 419-LYS--SER-566 DEL; 428-GLN--SER-566 DEL; SER-433; THR-446; THR-489; LYS-504; LYS-543 INS AND 563-ASN--SER-566 DEL; CHARACTERIZATION OF VARIANTS MISSLA CYS-282; LEU-292; 417-ASN-SER-418 DEL; THR-446; THR-489 AND LYS-543; VARIANT ARG-28; CHARACTERIZATION OF VARIANT ARG-28; FUNCTION; SUBCELLULAR LOCATION; INDUCTION; IDENTIFICATION IN THE REPLISOME COMPLEX; INTERACTION WITH MCM2; MCM7; PCNA AND TICRR;

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.