NM_000145.4(FSHR):c.219G>A (p.Glu73=) AND Ovarian dysgenesis 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000336327.5
Allele description [Variation Report for NM_000145.4(FSHR):c.219G>A (p.Glu73=)]
NM_000145.4(FSHR):c.219G>A (p.Glu73=)
Condition(s)
- Name:
- Ovarian dysgenesis 1 (ODG1)
- Synonyms:
- OVARIAN DYSGENESIS, HYPERGONADOTROPIC, AUTOSOMAL RECESSIVE; OVARIAN DYSGENESIS, HYPERGONADOTROPIC, WITH NORMAL KARYOTYPE; OVARIAN FAILURE, HYPERGONADOTROPIC; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0024463; MedGen: C0949595; Orphanet: 243; OMIM: 233300
-
Arachis hypogaea DNA, clone: AHGS41F13, genomic survey sequence
Arachis hypogaea DNA, clone: AHGS41F13, genomic survey sequencegi|387518599|dbj|DH962247.1|Nucleotide
-
Arachis hypogaea DNA, clone: KIAC12P17, genomic survey sequence
Arachis hypogaea DNA, clone: KIAC12P17, genomic survey sequencegi|387521343|dbj|DH965731.1|Nucleotide
-
Annotated Genomic for Nucleotide (Select 1889674209) (2)
Nucleotide
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Last Updated: Apr 9, 2023