NM_012082.4(ZFPM2):c.845C>T (p.Pro282Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004070159.1
Allele description [Variation Report for NM_012082.4(ZFPM2):c.845C>T (p.Pro282Leu)]
NM_012082.4(ZFPM2):c.845C>T (p.Pro282Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens family with sequence similarity 62 (C2 domain containing), member A...
Homo sapiens family with sequence similarity 62 (C2 domain containing), member A, mRNA (cDNA clone MGC:4422 IMAGE:2958094), complete cdsgi|13436457|gb|BC004998.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024