UniProtKB/Swiss-Prot Q96QB1: Variant p.Ser1209Cys

Rho GTPase-activating protein 7
Gene: DLC1
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Variant information Variant position:

1209 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 Cysteine (C) at position 1209 (S1209C, p.Ser1209Cys). 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 medium size and polar (C) 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 rs1044094 [ dbSNP | Ensembl ]

Sequence information Variant position:

1209 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:

1528 The length of the canonical sequence.
Location on the sequence:

AIMLLPDENREVLQTLLYFL S DVTAAVKENQMTPTNLAVCL 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                         AIMLLPDENREVLQTLLYFLSDVTAAVKENQMTPTNLAVCL

                              AIMLLPDENREVLQTLLYFLSDVTAAVKENQMTPTNLAVCL

Mouse                         AIMLLPDENREVLQTLLYFLSDVTAAVKENQMTPTNLAVCL

Rat                           AIMLLPDENREVLQTLLYFLSHVTAAVKENQMTPTNLAVCL

Bovine                        AIMLLPDENREVLQTLLYFLSDVTAAVKENQMTPTNLAVCL

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 – 1528	Rho GTPase-activating protein 7
Domain	1078 – 1284	Rho-GAP
Alternative sequence	464 – 1528	Missing. In isoform 5.
Alternative sequence	499 – 1528	Missing. In isoform 3.
Helix	1195 – 1213

Literature citations
Cloning, characterization, and chromosomal localization of a gene frequently deleted in human liver cancer (DLC-1) homologous to rat RhoGAP.
Yuan B.Z.; Miller M.J.; Keck C.L.; Zimonjic D.B.; Thorgeirsson S.S.; Popescu N.C.;
Cancer Res. 58:2196-2199(1998)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1); VARIANTS SER-712; VAL-1199 AND CYS-1209; Sequence variants of DLC1 in colorectal and ovarian tumours.
Wilson P.J.; McGlinn E.; Marsh A.; Evans T.; Arnold J.; Wright K.; Biden K.; Young J.; Wainwright B.; Wicking C.; Chenevix-Trench G.;
Hum. Mutat. 15:156-165(2000)
Cited for: VARIANTS SER-712; MET-791; ALA-959; GLN-998; ALA-1025; VAL-1199 AND CYS-1209;

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.