NM_001042492.3(NF1):c.8151G>A (p.Pro2717=) AND not specified
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Sep 9, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000216274.18
Allele description [Variation Report for NM_001042492.3(NF1):c.8151G>A (p.Pro2717=)]
NM_001042492.3(NF1):c.8151G>A (p.Pro2717=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: Mar 10, 2024