NM_002485.5(NBN):c.171+12A>G AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 17, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000443198.3
Allele description [Variation Report for NM_002485.5(NBN):c.171+12A>G]
NM_002485.5(NBN):c.171+12A>G
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
CERS3 [Eptesicus fuscus]
CERS3 [Eptesicus fuscus]Gene ID:103301954Gene
-
UXS1 [Neogale vison]
UXS1 [Neogale vison]Gene ID:122916412Gene
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024