NM_001039592.2(SPAG8):c.1151A>G (p.His384Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004218556.1
Allele description [Variation Report for NM_001039592.2(SPAG8):c.1151A>G (p.His384Arg)]
NM_001039592.2(SPAG8):c.1151A>G (p.His384Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
2292704[uid] (1)
Taxonomy
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Last Updated: May 26, 2024