NM_001080476.3(GRXCR1):c.358T>C (p.Phe120Leu) AND Autosomal recessive nonsyndromic hearing loss 25
- 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:
- RCV000287988.5
Allele description [Variation Report for NM_001080476.3(GRXCR1):c.358T>C (p.Phe120Leu)]
NM_001080476.3(GRXCR1):c.358T>C (p.Phe120Leu)
Condition(s)
-
Nucleotide Links for Protein (Select 154091310) (3)
Nucleotide
-
eggcsite.comhA6 (0)
BioProject
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Last Updated: Apr 9, 2023