NM_007144.3(PCGF2):c.721G>A (p.Val241Met) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003349032.2
Allele description [Variation Report for NM_007144.3(PCGF2):c.721G>A (p.Val241Met)]
NM_007144.3(PCGF2):c.721G>A (p.Val241Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
PREDICTED: Homo sapiens CD109 molecule (CD109), transcript variant X9, mRNA
PREDICTED: Homo sapiens CD109 molecule (CD109), transcript variant X9, mRNAgi|2462606135|ref|XM_054354306.1|Nucleotide
-
LOC121740656 [Homo sapiens]
LOC121740656 [Homo sapiens]Gene ID:121740656Gene
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Last Updated: Sep 29, 2024