NM_138691.3(TMC1):c.*10T>C AND Autosomal dominant nonsyndromic hearing loss 36
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001166710.4
Allele description [Variation Report for NM_138691.3(TMC1):c.*10T>C]
NM_138691.3(TMC1):c.*10T>C
Condition(s)
-
"Am J Health Syst Pharm"[journal] (335)
PMC
-
Profile neighbors for GEO Profiles (Select 61623002) (104)
GEO Profiles
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Apr 9, 2023