NM_001042492.3(NF1):c.3498C>T (p.Gly1166=) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Dec 12, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000680334.11
Allele description [Variation Report for NM_001042492.3(NF1):c.3498C>T (p.Gly1166=)]
NM_001042492.3(NF1):c.3498C>T (p.Gly1166=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
SMG1P2 SMG1 pseudogene 2 [Homo sapiens]
SMG1P2 SMG1 pseudogene 2 [Homo sapiens]Gene ID:440354Gene
-
Gene Links for dbVar (Select 45752914) (1)
Gene
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Last Updated: Mar 10, 2024