UniProtKB/SwissProt variant VAR

Variant information

Variant position:

39

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 Valine (V) to Leucine (L) at position 39 (V39L, p.Val39Leu).

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

Variant description:

Probable disease-associated variant found in patients with dilated cardiomyopathy; results in significantly reduced transactivation activity.

Any additional useful information about the variant.

Other resources:

Links to websites of interest for the variant.

Variant rs1139241 [ dbSNP | Ensembl ]

Sequence information

Variant position:

39

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

Protein sequence length:

442

The length of the canonical sequence.

Location on the sequence:

EAGGPGAFMHGAGAASSPVY V PTPRVPSSVLGLSYLQGGGA

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                         EAGGPGAFMHGAGAASSPVYVPTPRVPSSVLGLSYLQGGGA

                              EAGGPGAFMHGAGAASSPVYVPTPRVPSSVLGLSYLQGGGG

Mouse                         EAGGPGAFMHSAGAASSPVYVPTPRVPSSVLGLSYLQGGGS

Rat                           EAGGPGAFMHSAGAASSPVYVPTPRVPSSVLGLSYLQGGGS

Xenopus laevis                E--GTGSFMHSATAATSPVYVPTTRVSSMIHSLPYLQ----

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 – 442	Transcription factor GATA-4

Literature citations

Identification of a GATA motif in the cardiac alpha-myosin heavy-chain-encoding gene and isolation of a human GATA-4 cDNA.
Huang W.Y.; Cukerman E.; Liew C.C.;
Gene 155:219-223(1995)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1); VARIANT LEU-39;

Prevalence and spectrum of GATA4 mutations associated with sporadic dilated cardiomyopathy.
Li J.; Liu W.D.; Yang Z.L.; Yuan F.; Xu L.; Li R.G.; Yang Y.Q.;
Gene 548:174-181(2014)
Cited for: INVOLVEMENT IN CMD; VARIANTS LEU-39; GLN-226 AND SER-279; CHARACTERIZATION OF VARIANTS LEU-39; GLN-226 AND SER-279;

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P43694: Variant p.Val39Leu