NM_001904.4(CTNNB1):c.860A>G (p.Asn287Ser) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002517580.2
Allele description [Variation Report for NM_001904.4(CTNNB1):c.860A>G (p.Asn287Ser)]
NM_001904.4(CTNNB1):c.860A>G (p.Asn287Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens testis specific protein Y-linked 9 (TSPY9), mRNA
Homo sapiens testis specific protein Y-linked 9 (TSPY9), mRNAgi|2099742734|ref|NM_001396063.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024