NM_001267046.2(FRMD6):c.1148G>A (p.Arg383His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004326491.1
Allele description [Variation Report for NM_001267046.2(FRMD6):c.1148G>A (p.Arg383His)]
NM_001267046.2(FRMD6):c.1148G>A (p.Arg383His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens coiled-coil domain containing 61 (CCDC61), mRNA
Homo sapiens coiled-coil domain containing 61 (CCDC61), mRNAgi|1519244383|ref|NM_001267723.2|Nucleotide
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Last Updated: Oct 8, 2024