NM_000260.4(MYO7A):c.3638G>A (p.Arg1213Gln) AND Autosomal recessive nonsyndromic hearing loss 2
- 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:
- RCV001111014.4
Allele description [Variation Report for NM_000260.4(MYO7A):c.3638G>A (p.Arg1213Gln)]
NM_000260.4(MYO7A):c.3638G>A (p.Arg1213Gln)
Condition(s)
-
Homo sapiens isolate C10orf2_P24 mitochondrial twinkle protein gene, complete cd...
Homo sapiens isolate C10orf2_P24 mitochondrial twinkle protein gene, complete cds; nuclear gene for mitochondrial productgi|311349729|gb|HQ206142.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Mar 16, 2024