NM_181723.3(MICU3):c.259G>C (p.Gly87Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004224186.1
Allele description [Variation Report for NM_181723.3(MICU3):c.259G>C (p.Gly87Arg)]
NM_181723.3(MICU3):c.259G>C (p.Gly87Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
FANCI FA complementation group I [Homo sapiens]
FANCI FA complementation group I [Homo sapiens]Gene ID:55215Gene
-
Gene for MedGen (Select 323016) (1)
Gene
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Last Updated: Oct 26, 2024