NM_000044.6(AR):c.2017A>G (p.Ile673Val) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004366514.1
Allele description [Variation Report for NM_000044.6(AR):c.2017A>G (p.Ile673Val)]
NM_000044.6(AR):c.2017A>G (p.Ile673Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
cation channel sperm-associated protein 4 [Homo sapiens]
cation channel sperm-associated protein 4 [Homo sapiens]gi|62988334|ref|NP_937770.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024