NM_001038603.3(MARVELD2):c.1049T>C (p.Val350Ala) AND Autosomal recessive nonsyndromic hearing loss 49
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000374495.5
Allele description [Variation Report for NM_001038603.3(MARVELD2):c.1049T>C (p.Val350Ala)]
NM_001038603.3(MARVELD2):c.1049T>C (p.Val350Ala)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023