NM_024830.5(LPCAT1):c.328G>T (p.Gly110Cys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004351250.1
Allele description [Variation Report for NM_024830.5(LPCAT1):c.328G>T (p.Gly110Cys)]
NM_024830.5(LPCAT1):c.328G>T (p.Gly110Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens high mobility group nucleosome binding domain 1 (HMGN1), mRNA
Homo sapiens high mobility group nucleosome binding domain 1 (HMGN1), mRNAgi|1519313719|ref|NM_004965.7|Nucleotide
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Last Updated: Oct 8, 2024