NM_006901.4(MYO9A):c.6709A>G (p.Thr2237Ala) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004462259.1
Allele description [Variation Report for NM_006901.4(MYO9A):c.6709A>G (p.Thr2237Ala)]
NM_006901.4(MYO9A):c.6709A>G (p.Thr2237Ala)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
au64h02.y1 Schneider fetal brain 00004 Homo sapiens cDNA clone IMAGE:2519571 5',...
au64h02.y1 Schneider fetal brain 00004 Homo sapiens cDNA clone IMAGE:2519571 5', mRNA sequencegi|5665041|gnl|dbEST|3051051|gb|AI9 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024