NM_000260.4(MYO7A):c.3855C>T (p.Asn1285=) AND Usher syndrome type 1B
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 16, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001279795.1
Allele description [Variation Report for NM_000260.4(MYO7A):c.3855C>T (p.Asn1285=)]
NM_000260.4(MYO7A):c.3855C>T (p.Asn1285=)
Condition(s)
- Name:
- Usher syndrome type 1B (USH1B)
- Synonyms:
- Usher syndrome type IB
- Identifiers:
- MONDO: MONDO:0700087; MedGen: C2931206
-
Vollenhovia emeryi isolate JJ31 cytochrome c oxidase subunit I gene, partial cds...
Vollenhovia emeryi isolate JJ31 cytochrome c oxidase subunit I gene, partial cds; mitochondrialgi|574609069|gb|KF815852.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Feb 20, 2024