UniProtKB/Swiss-Prot Q5H9L4: Variant p.Ser308Gly

Transcription initiation factor TFIID subunit 7-like
Gene: TAF7L
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Variant information Variant position:

308 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 Glycine (G) at position 308 (S308G, p.Ser308Gly). 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 glycine (G) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

0 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 rs35899692 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

TKEIESQGSIPGFLISSGMS S HKQGHTSSEYDMLREMFSDS 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                         TKEIESQGSIPGFLISSGMSSHKQGHTSSEYDMLREMFSDS

Mouse                         AKEIESQGSMP---TTPGI-SQMGGASLSDYDVFREMMGDS

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 – 462	Transcription initiation factor TFIID subunit 7-like

Literature citations
The role of the testis-specific gene hTAF7L in the aetiology of male infertility.
Stouffs K.; Willems A.; Lissens W.; Tournaye H.; Van Steirteghem A.; Liebaers I.;
Mol. Hum. Reprod. 12:263-267(2006)
Cited for: VARIANTS LYS-61; GLY-308; 350-ASP-GLU-351 DEL AND HIS-458; Mutation analysis of the X-chromosome linked, testis-specific TAF7L gene in spermatogenic failure.
Akinloye O.; Gromoll J.; Callies C.; Nieschlag E.; Simoni M.;
Andrologia 39:190-195(2007)
Cited for: VARIANTS GLY-308; 350-ASP-GLU-351 DEL AND HIS-458;

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.