NM_015355.4(SUZ12):c.2168A>G (p.Glu723Gly) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003364599.2
Allele description [Variation Report for NM_015355.4(SUZ12):c.2168A>G (p.Glu723Gly)]
NM_015355.4(SUZ12):c.2168A>G (p.Glu723Gly)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
BX113648 NCI_CGAP_Gas4 Homo sapiens cDNA clone IMAGp998P236111; IMAGE:2457478 3'...
BX113648 NCI_CGAP_Gas4 Homo sapiens cDNA clone IMAGp998P236111; IMAGE:2457478 3', mRNA sequencegi|27838366|gnl|dbEST|16744184|emb| 648.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024