NM_016239.4(MYO15A):c.5557C>G (p.His1853Asp) AND Autosomal recessive nonsyndromic hearing loss 3
- Germline classification:
- Uncertain significance (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001771831.1
Allele description [Variation Report for NM_016239.4(MYO15A):c.5557C>G (p.His1853Asp)]
NM_016239.4(MYO15A):c.5557C>G (p.His1853Asp)
Condition(s)
-
OMIM(Genes) for MedGen (Select 816133) (1)
OMIM
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hus1+-like [Homo sapiens]
hus1+-like [Homo sapiens]gi|2980665|emb|CAA76518.1|Protein
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Homo sapiens chromosome 18, clone RP11-650P15, complete sequence
Homo sapiens chromosome 18, clone RP11-650P15, complete sequencegi|19033940|gnl|WIBR|L5633|gb|AC021 |Nucleotide
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LOC127405749 [Homo sapiens]
LOC127405749 [Homo sapiens]Gene ID:127405749Gene
-
Cytochrome P450, partial [Anopheles funestus]
Cytochrome P450, partial [Anopheles funestus]gi|992369832|gb|AMH87369.1|Protein
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023