NM_001039569.2(AP1S3):c.97C>T (p.Arg33Trp) AND AP1S3-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 2, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003927448.1
Allele description [Variation Report for NM_001039569.2(AP1S3):c.97C>T (p.Arg33Trp)]
NM_001039569.2(AP1S3):c.97C>T (p.Arg33Trp)
Condition(s)
- Name:
- AP1S3-related disorder
- Synonyms:
- AP1S3-related condition
- Identifiers:
-
Homo sapiens Meis homeobox 2 (MEIS2), transcript variant f, mRNA
Homo sapiens Meis homeobox 2 (MEIS2), transcript variant f, mRNAgi|27502374|ref|NM_002399.2|Nucleotide
-
202255[uid] (1)
Taxonomy
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024