NM_002585.4(PBX1):c.997+11dup AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Aug 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002593023.2
Allele description [Variation Report for NM_002585.4(PBX1):c.997+11dup]
NM_002585.4(PBX1):c.997+11dup
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Krueppel-like factor 5 isoform X1 [Homo sapiens]
Krueppel-like factor 5 isoform X1 [Homo sapiens]gi|2217294898|ref|XP_047286509.1|Protein
-
PREDICTED: Homo sapiens glycine C-acetyltransferase (GCAT), transcript variant X...
PREDICTED: Homo sapiens glycine C-acetyltransferase (GCAT), transcript variant X6, mRNAgi|2217339219|ref|XM_005261410.5|Nucleotide
-
ClinVar for Gene (Select 124416842) (5)
ClinVar
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See more...Assertion and evidence details
Last Updated: Feb 28, 2024