UniProtKB/SwissProt variant VAR

Variant information

Variant position:

929

The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:

LP/P [Disclaimer]

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 Glutamine (Q) to Proline (P) at position 929 (Q929P, p.Gln929Pro).

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 polar (Q) to medium size and hydrophobic (P)

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:

In KMIN.

Any additional useful information about the variant.

Sequence information

Variant position:

929

The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:

1017

The length of the canonical sequence.

Location on the sequence:

QEGRVASLVSWDRFTSLQQA Q DLVSCLGGPVLSGVCRHLAA

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                         QEGRV--ASLVSWDRFT-SLQQAQDLVSCLGGPVLSGVCRHLAA

Mouse                         QQGRV--ASLVSWDRFT-SLQQAQDLVSCLGGPVLSGVCRR

Zebrafish                     QEGRV--CALINWERFS-TPQQAQSLVACLGGHFLSGVFLR

Caenorhabditis elegans        KHNET--NRECSWKQFPMGAEDCVSFFQCIPRPALILILRR

Slime mold                    HNGCE--ARGVNW-KST-SLEQLSIISKCLGGKLIAFISRL

Fission yeast                 EHQRKTFCVGLNW-SYT-C-EMLLEIVDCINDNGLAQIFLA

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 – 1017	Fanconi-associated nuclease 1
Domain	895 – 1007	VRR-NUC
Alternative sequence	534 – 1017	Missing. In isoform 2.
Helix	925 – 949

Literature citations

FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair.
Zhou W.; Otto E.A.; Cluckey A.; Airik R.; Hurd T.W.; Chaki M.; Diaz K.; Lach F.P.; Bennett G.R.; Gee H.Y.; Ghosh A.K.; Natarajan S.; Thongthip S.; Veturi U.; Allen S.J.; Janssen S.; Ramaswami G.; Dixon J.; Burkhalter F.; Spoendlin M.; Moch H.; Mihatsch M.J.; Verine J.; Reade R.; Soliman H.; Godin M.; Kiss D.; Monga G.; Mazzucco G.; Amann K.; Artunc F.; Newland R.C.; Wiech T.; Zschiedrich S.; Huber T.B.; Friedl A.; Slaats G.G.; Joles J.A.; Goldschmeding R.; Washburn J.; Giles R.H.; Levy S.; Smogorzewska A.; Hildebrandt F.;
Nat. Genet. 44:910-915(2012)
Cited for: VARIANTS KMIN ARG-871; PRO-929; ASP-937 AND ASN-960;

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9Y2M0: Variant p.Gln929Pro