NM_004999.4(MYO6):c.1049T>C (p.Ile350Thr) AND Autosomal recessive nonsyndromic hearing loss 37
- 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:
- RCV001159445.4
Allele description [Variation Report for NM_004999.4(MYO6):c.1049T>C (p.Ile350Thr)]
NM_004999.4(MYO6):c.1049T>C (p.Ile350Thr)
Condition(s)
-
PREDICTED: Homo sapiens polypeptide N-acetylgalactosaminyltransferase 14 (GALNT1...
PREDICTED: Homo sapiens polypeptide N-acetylgalactosaminyltransferase 14 (GALNT14), transcript variant X7, misc_RNAgi|2462577152|ref|XR_008486519.1|Nucleotide
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Last Updated: Apr 9, 2023