NM_000255.4(MMUT):c.423G>A (p.Ala141=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 31, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000612888.1
Allele description [Variation Report for NM_000255.4(MMUT):c.423G>A (p.Ala141=)]
NM_000255.4(MMUT):c.423G>A (p.Ala141=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
C12H20orf96 [Equus quagga]
C12H20orf96 [Equus quagga]Gene ID:124248127Gene
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024