NM_001042492.3(NF1):c.4635C>T (p.Tyr1545=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 11, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000613133.1
Allele description [Variation Report for NM_001042492.3(NF1):c.4635C>T (p.Tyr1545=)]
NM_001042492.3(NF1):c.4635C>T (p.Tyr1545=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens p53-induced protein with RING-H2 variant D (RCHY1) mRNA, complete c...
Homo sapiens p53-induced protein with RING-H2 variant D (RCHY1) mRNA, complete cdsgi|289900829|gb|GU937000.1|Nucleotide
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Last Updated: Sep 29, 2024