NM_016239.4(MYO15A):c.*117C>A AND Autosomal recessive nonsyndromic hearing loss 3
- 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:
- RCV000370420.5
Allele description [Variation Report for NM_016239.4(MYO15A):c.*117C>A]
NM_016239.4(MYO15A):c.*117C>A
Condition(s)
-
Homo sapiens uncharacterized LOC102724434 (LOC102724434), transcript variant 3, ...
Homo sapiens uncharacterized LOC102724434 (LOC102724434), transcript variant 3, long non-coding RNAgi|756141059|ref|NR_130923.1|Nucleotide
-
RecName: Full=Probable chorismate pyruvate-lyase; Short=CL; Short=CPL
RecName: Full=Probable chorismate pyruvate-lyase; Short=CL; Short=CPLgi|81636915|sp|Q9CMB5.1|UBIC_PASMUProtein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2023