UniProtKB/Swiss-Prot P61758: Variant p.Val123Met

Prefoldin subunit 3
Gene: VBP1
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Variant information Variant position:

123 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 Valine (V) to Methionine (M) at position 123 (V123M, p.Val123Met). 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 hydrophobic. 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 rs572013 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

TRFLLADNLYCKASVPPTDK V CLWLGANVMLEYDIDEAQAL 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                         TRFLLADNLYCKASVPPTD-----KVCLWLGANVMLEYDIDEAQAL

Mouse                         TRFLLADNLYCKASVPPTD-----KVCLWLGANVMLEYDID

Bovine                        TRFLLADNLYCKASVPPTD-----KVCLWLGANVMLEYDID

Caenorhabditis elegans        TTFLLSDDVYTKATVQKPE-----KVSIWLGANVMVEYDLE

Drosophila                    TQFLLSDQVFIKTLVPPTK-----TVYLWLGASVMLEYPLD

Slime mold                    VQYELSEGVYSSAQVNEPK-----SIYLWLGANVMLEYSFE

Baker's yeast                 LHYQLNDTLYTKAQVDIPEDRADLKVGLWLGADVMLEYPID

Fission yeast                 VTYELNDTLNAKAEVEAKD-----NVYLWLGANVMLEYTVE

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	2 – 197	Prefoldin subunit 3

Literature citations
The DNA sequence of the human X chromosome.
Ross M.T.; Grafham D.V.; Coffey A.J.; Scherer S.; McLay K.; Muzny D.; Platzer M.; Howell G.R.; Burrows C.; Bird C.P.; Frankish A.; Lovell F.L.; Howe K.L.; Ashurst J.L.; Fulton R.S.; Sudbrak R.; Wen G.; Jones M.C.; Hurles M.E.; Andrews T.D.; Scott C.E.; Searle S.; Ramser J.; Whittaker A.; Deadman R.; Carter N.P.; Hunt S.E.; Chen R.; Cree A.; Gunaratne P.; Havlak P.; Hodgson A.; Metzker M.L.; Richards S.; Scott G.; Steffen D.; Sodergren E.; Wheeler D.A.; Worley K.C.; Ainscough R.; Ambrose K.D.; Ansari-Lari M.A.; Aradhya S.; Ashwell R.I.; Babbage A.K.; Bagguley C.L.; Ballabio A.; Banerjee R.; Barker G.E.; Barlow K.F.; Barrett I.P.; Bates K.N.; Beare D.M.; Beasley H.; Beasley O.; Beck A.; Bethel G.; Blechschmidt K.; Brady N.; Bray-Allen S.; Bridgeman A.M.; Brown A.J.; Brown M.J.; Bonnin D.; Bruford E.A.; Buhay C.; Burch P.; Burford D.; Burgess J.; Burrill W.; Burton J.; Bye J.M.; Carder C.; Carrel L.; Chako J.; Chapman J.C.; Chavez D.; Chen E.; Chen G.; Chen Y.; Chen Z.; Chinault C.; Ciccodicola A.; Clark S.Y.; Clarke G.; Clee C.M.; Clegg S.; Clerc-Blankenburg K.; Clifford K.; Cobley V.; Cole C.G.; Conquer J.S.; Corby N.; Connor R.E.; David R.; Davies J.; Davis C.; Davis J.; Delgado O.; Deshazo D.; Dhami P.; Ding Y.; Dinh H.; Dodsworth S.; Draper H.; Dugan-Rocha S.; Dunham A.; Dunn M.; Durbin K.J.; Dutta I.; Eades T.; Ellwood M.; Emery-Cohen A.; Errington H.; Evans K.L.; Faulkner L.; Francis F.; Frankland J.; Fraser A.E.; Galgoczy P.; Gilbert J.; Gill R.; Gloeckner G.; Gregory S.G.; Gribble S.; Griffiths C.; Grocock R.; Gu Y.; Gwilliam R.; Hamilton C.; Hart E.A.; Hawes A.; Heath P.D.; Heitmann K.; Hennig S.; Hernandez J.; Hinzmann B.; Ho S.; Hoffs M.; Howden P.J.; Huckle E.J.; Hume J.; Hunt P.J.; Hunt A.R.; Isherwood J.; Jacob L.; Johnson D.; Jones S.; de Jong P.J.; Joseph S.S.; Keenan S.; Kelly S.; Kershaw J.K.; Khan Z.; Kioschis P.; Klages S.; Knights A.J.; Kosiura A.; Kovar-Smith C.; Laird G.K.; Langford C.; Lawlor S.; Leversha M.; Lewis L.; Liu W.; Lloyd C.; Lloyd D.M.; Loulseged H.; Loveland J.E.; Lovell J.D.; Lozado R.; Lu J.; Lyne R.; Ma J.; Maheshwari M.; Matthews L.H.; McDowall J.; McLaren S.; McMurray A.; Meidl P.; Meitinger T.; Milne S.; Miner G.; Mistry S.L.; Morgan M.; Morris S.; Mueller I.; Mullikin J.C.; Nguyen N.; Nordsiek G.; Nyakatura G.; O'dell C.N.; Okwuonu G.; Palmer S.; Pandian R.; Parker D.; Parrish J.; Pasternak S.; Patel D.; Pearce A.V.; Pearson D.M.; Pelan S.E.; Perez L.; Porter K.M.; Ramsey Y.; Reichwald K.; Rhodes S.; Ridler K.A.; Schlessinger D.; Schueler M.G.; Sehra H.K.; Shaw-Smith C.; Shen H.; Sheridan E.M.; Shownkeen R.; Skuce C.D.; Smith M.L.; Sotheran E.C.; Steingruber H.E.; Steward C.A.; Storey R.; Swann R.M.; Swarbreck D.; Tabor P.E.; Taudien S.; Taylor T.; Teague B.; Thomas K.; Thorpe A.; Timms K.; Tracey A.; Trevanion S.; Tromans A.C.; d'Urso M.; Verduzco D.; Villasana D.; Waldron L.; Wall M.; Wang Q.; Warren J.; Warry G.L.; Wei X.; West A.; Whitehead S.L.; Whiteley M.N.; Wilkinson J.E.; Willey D.L.; Williams G.; Williams L.; Williamson A.; Williamson H.; Wilming L.; Woodmansey R.L.; Wray P.W.; Yen J.; Zhang J.; Zhou J.; Zoghbi H.; Zorilla S.; Buck D.; Reinhardt R.; Poustka A.; Rosenthal A.; Lehrach H.; Meindl A.; Minx P.J.; Hillier L.W.; Willard H.F.; Wilson R.K.; Waterston R.H.; Rice C.M.; Vaudin M.; Coulson A.; Nelson D.L.; Weinstock G.; Sulston J.E.; Durbin R.M.; Hubbard T.; Gibbs R.A.; Beck S.; Rogers J.; Bentley D.R.;
Nature 434:325-337(2005)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]; VARIANT MET-123;

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.