UniProtKB/Swiss-Prot P22888: Variant p.Asn312Ser

Lutropin-choriogonadotropic hormone receptor
Gene: LHCGR
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Variant information Variant position:

312 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 Asparagine (N) to Serine (S) at position 312 (N312S, p.Asn312Ser). 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 (N) to small size and polar (S) 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 rs2293275 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

FSHSISENFSKQCESTVRKV N NKTLYSSMLAESELSGWDYE 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                         FSHSISENFSKQCESTVRKVNNKTL------------------------------YSSMLAESELSGWDYE

Mouse                         FSFSIFENFSKQCESTVREANNETL----------------

Rat                           FSFSIFENFSKQCESTVRKADNETL----------------

Pig                           FSFSIFKNFSKQCESTARRPNNETL----------------

Bovine                        FSFSIFKNFSKQCESTARRPNNETL----------------

Chicken                       SLLSIFDNFSKQCESTMRKPASEVFYRDASSNTSLWPAEKH

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	27 – 699	Lutropin-choriogonadotropic hormone receptor
Topological domain	27 – 363	Extracellular
Modified residue	331 – 331	Sulfotyrosine
Glycosylation	299 – 299	N-linked (GlcNAc...) asparagine
Glycosylation	313 – 313	N-linked (GlcNAc...) asparagine
Mutagenesis	331 – 331	Y -> F. Reduces intracellular cAMP accumulation.

Literature citations
Cloning and sequencing of human LH/hCG receptor cDNA.
Minegish T.; Nakamura K.; Takakura Y.; Miyamoto K.; Hasegawa Y.; Ibuki Y.; Igarashi M.;
Biochem. Biophys. Res. Commun. 172:1049-1054(1990)
Cited for: NUCLEOTIDE SEQUENCE [MRNA]; VARIANT SER-312; Structure of the human luteinizing hormone-choriogonadotropin receptor gene: unusual promoter and 5' non-coding regions.
Atger M.; Misrahi M.; Sar S.; Leflem L.; Dessen P.; Milgrom E.;
Mol. Cell. Endocrinol. 111:113-123(1995)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANTS LEU-GLN-18 INS AND SER-312;

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.