NM_053279.3(FAM167A):c.600C>T (p.Gly200=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003436730.8
Allele description
NM_053279.3(FAM167A):c.600C>T (p.Gly200=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PREDICTED: Homo sapiens uncharacterized lncRNA (LOC100505711), transcript varian...
PREDICTED: Homo sapiens uncharacterized lncRNA (LOC100505711), transcript variant X1, ncRNAgi|2217530889|ref|XR_007076769.1|Nucleotide
-
LOC130058600 [Homo sapiens]
LOC130058600 [Homo sapiens]Gene ID:130058600Gene
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Last Updated: Aug 4, 2024