NM_033515.3(ARHGAP18):c.1739G>A (p.Arg580Gln) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 16, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004236768.1
Allele description [Variation Report for NM_033515.3(ARHGAP18):c.1739G>A (p.Arg580Gln)]
NM_033515.3(ARHGAP18):c.1739G>A (p.Arg580Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
ATP synthase subunit C lysine N-methyltransferase isoform 1 [Homo sapiens]
ATP synthase subunit C lysine N-methyltransferase isoform 1 [Homo sapiens]gi|154240720|ref|NP_954584.2|Protein
-
fragile X mental retardation syndrome-related protein 2, partial [Lepus europaeu...
fragile X mental retardation syndrome-related protein 2, partial [Lepus europaeus]gi|1528991740|gb|AZI94602.1|Protein
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Last Updated: Jul 15, 2024