NM_002485.5(NBN):c.1398-112C>T AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 2, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001585623.3
Allele description [Variation Report for NM_002485.5(NBN):c.1398-112C>T]
NM_002485.5(NBN):c.1398-112C>T
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens complement C5 (C5), transcript variant 1, mRNA
Homo sapiens complement C5 (C5), transcript variant 1, mRNAgi|1732746243|ref|NM_001735.3|Nucleotide
-
Homo sapiens mRNA; cDNA DKFZp727M231 (from clone DKFZp727M231)
Homo sapiens mRNA; cDNA DKFZp727M231 (from clone DKFZp727M231)gi|5911956|emb|AL117480.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023