UniProtKB/SwissProt variant VAR

Variant information

Variant position:

241

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 Lysine (K) at position 241 (Q241K, p.Gln241Lys).

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 large size and basic (K)

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 HEMB.

Any additional useful information about the variant.

Sequence information

Variant position:

241

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

Protein sequence length:

461

The length of the canonical sequence.

Location on the sequence:

FNDFTRVVGGEDAKPGQFPW Q VVLNGKVDAFCGGSIVNEKW

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                         FNDFTRVVGGEDAKPGQFPWQV-VLNGKVDAFCGGSIVNEKW

                              LNDFTRVVGGKDAKPGQFPWQV-LLNGKVDAFCGGSIINEK

Chimpanzee                    FNDFTRVVGGEDAKPGQFPWQV-VLNGKVDAFCGGSIVNEK

Mouse                         LNDFTRVVGGENAKPGQIPWQV-ILNGEIEAFCGGAIINEK

Rat                           INDFTRVVGGENAKPGQIPWQV-ILNGEIEAFCGGAIINEK

Bovine                        FDEFSRVVGGEDAERGQFPWQV-LLHGEIAAFCGGSIVNEK

Cat                           LNDLTRIVGGKTAKPGQFPWQV-LLKGKIDAFCGGSIINEK

Chicken                       TKNDTRVVGGYDSVKGQLPWQVHLVDSRGLGFCGGSIINEK

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	47 – 461	Coagulation factor IX
Chain	227 – 461	Coagulation factor IXa heavy chain
Domain	227 – 459	Peptidase S1
Glycosylation	225 – 225	O-linked (GalNAc...) threonine
Disulfide bond	178 – 335	Interchain (between light and heavy chains)
Beta strand	241 – 248

Literature citations

Molecular pathology of haemophilia B in Turkish patients: identification of a large deletion and 33 independent point mutations.
Onay U.V.; Kavakli K.; Kilinc Y.; Gurgey A.; Aktuglu G.; Kemahli S.; Ozbek U.; Caglayan S.H.;
Br. J. Haematol. 120:656-659(2003)
Cited for: VARIANTS HEMB TYR-28; LEU-43; GLN-43; SER-52; ASP-106; LYS-124; TYR-134; GLN-226; GLY-226; TRP-226; LYS-241; TYR-252; GLN-294; PHE-316; ARG-318; GLY-379; ILE-383; PHE-383; ILE-395; PHE-396; ARG-407 AND GLU-412;

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P00740: Variant p.Gln241Lys