NM_012369.3(OR2F1):c.737C>T (p.Thr246Ile) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 11, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004124945.1
Allele description [Variation Report for NM_012369.3(OR2F1):c.737C>T (p.Thr246Ile)]
NM_012369.3(OR2F1):c.737C>T (p.Thr246Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
SLC9A1 solute carrier family 9 member A1 [Homo sapiens]
SLC9A1 solute carrier family 9 member A1 [Homo sapiens]Gene ID:6548Gene
-
Gene Links for GEO Profiles (Select 69143212) (1)
Gene
-
txid1428862[Organism:noexp] (3)
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Last Updated: Nov 10, 2024