NM_001145809.2(MYH14):c.2694+30T>C AND Autosomal dominant nonsyndromic hearing loss 4A
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 5, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001776261.2
Allele description [Variation Report for NM_001145809.2(MYH14):c.2694+30T>C]
NM_001145809.2(MYH14):c.2694+30T>C
Condition(s)
-
tyrA [Escherichia coli str. K-12 substr. MG1655]
tyrA [Escherichia coli str. K-12 substr. MG1655]Gene ID:947115Gene
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023