UniProtKB/SwissProt variant VAR

Variant information

Variant position:

76

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 Arginine (R) to Cysteine (C) at position 76 (R76C, p.Arg76Cys).

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 large size and basic (R) to medium size and polar (C)

The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:

-3

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 CTRCT1.

Any additional useful information about the variant.

Sequence information

Variant position:

76

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

Protein sequence length:

433

The length of the canonical sequence.

Location on the sequence:

TQQPGCENVCYDEAFPISHI R LWVLQIIFVSTPSLMYVGHA

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                         TQQPGCENVCYDEAFPISHIRLWVLQIIFVSTPSLMYVGHA

Mouse                         TQQPGCENVCYDEAFPISHIRLWVLQIIFVSTPSLMYVGHA

Rat                           TQQPGCENVCYDEAFPISHIRLWVLQIIFVSTPSLMYVGHA

Sheep                         TQQPGCENVCYDEAFPISHIRLWVLQIIFVSTPSLVYVGHA

Chicken                       TQQPGCENVCYDEAFPISHIRLWVLQIIFVSTPSLVYFGHA

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 – 433	Gap junction alpha-8 protein
Transmembrane	72 – 92	Helical
Disulfide bond	54 – 194
Disulfide bond	61 – 188
Disulfide bond	65 – 183

Literature citations

Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes.
Reis L.M.; Tyler R.C.; Muheisen S.; Raggio V.; Salviati L.; Han D.P.; Costakos D.; Yonath H.; Hall S.; Power P.; Semina E.V.;
Hum. Genet. 132:761-770(2013)
Cited for: VARIANTS CTRCT1 GLY-67 AND CYS-76; VARIANT MET-247;

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P48165: Variant p.Arg76Cys