NM_001324144.2(ZNF41):c.1578T>A (p.Ala526=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 22, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004022122.1
Allele description [Variation Report for NM_001324144.2(ZNF41):c.1578T>A (p.Ala526=)]
NM_001324144.2(ZNF41):c.1578T>A (p.Ala526=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens small ubiquitin like modifier 1 (SUMO1), transcript variant 3, mRNA
Homo sapiens small ubiquitin like modifier 1 (SUMO1), transcript variant 3, mRNAgi|1701108504|ref|NM_001005782.2|Nucleotide
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solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 [Hom...
solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 [Homo sapiens]gi|119571608|gb|EAW51223.1||gnl|WGS |hCP43521Protein
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Last Updated: Oct 20, 2024