NM_080680.3(COL11A2):c.3794A>G (p.Asn1265Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002559482.1
Allele description [Variation Report for NM_080680.3(COL11A2):c.3794A>G (p.Asn1265Ser)]
NM_080680.3(COL11A2):c.3794A>G (p.Asn1265Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
USH2A-AS2 USH2A antisense RNA 2 [Homo sapiens]
USH2A-AS2 USH2A antisense RNA 2 [Homo sapiens]Gene ID:102723833Gene
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See more...Assertion and evidence details
Last Updated: Oct 14, 2023