NM_001371596.2(MFSD8):c.553+20C>T AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 13, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000126759.3
Allele description [Variation Report for NM_001371596.2(MFSD8):c.553+20C>T]
NM_001371596.2(MFSD8):c.553+20C>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens transmembrane protein 37 (TMEM37), mRNA
Homo sapiens transmembrane protein 37 (TMEM37), mRNAgi|1519315886|ref|NM_183240.3|Nucleotide
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Last Updated: Feb 20, 2024