NM_206933.4(USH2A):c.9413G>C (p.Gly3138Ala) AND Hearing impairment
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 12, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001375065.3
Allele description [Variation Report for NM_206933.4(USH2A):c.9413G>C (p.Gly3138Ala)]
NM_206933.4(USH2A):c.9413G>C (p.Gly3138Ala)
Condition(s)
- Name:
- Hearing impairment
- Identifiers:
- MONDO: MONDO:0005365; MedGen: C1384666; Human Phenotype Ontology: HP:0000365
-
Rattus norvegicus armadillo repeat containing, X-linked 2, mRNA (cDNA clone MGC:...
Rattus norvegicus armadillo repeat containing, X-linked 2, mRNA (cDNA clone MGC:93762 IMAGE:7108660), complete cdsgi|51980583|gb|BC081886.1|Nucleotide
-
PREDICTED: Mus musculus WAP, follistatin/kazal, immunoglobulin, kunitz and netri...
PREDICTED: Mus musculus WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 (Wfikkn2), transcript variant X4, mRNAgi|1907082011|ref|XM_006533500.5|Nucleotide
-
cas6f [Selenomonas ruminantium subsp. ruminantium ATCC 12561]
cas6f [Selenomonas ruminantium subsp. ruminantium ATCC 12561]Gene ID:61462412Gene
-
cas6f [Pseudoalteromonas shioyasakiensis]
cas6f [Pseudoalteromonas shioyasakiensis]Gene ID:29845123Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024