NM_006898.5(HOXD3):c.559A>C (p.Lys187Gln) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 31, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004328506.1
Allele description [Variation Report for NM_006898.5(HOXD3):c.559A>C (p.Lys187Gln)]
NM_006898.5(HOXD3):c.559A>C (p.Lys187Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens clustered mitochondria homolog (CLUH), transcript variant 2, mRNA
Homo sapiens clustered mitochondria homolog (CLUH), transcript variant 2, mRNAgi|1489866047|ref|NM_015229.4|Nucleotide
-
Homo sapiens cDNA FLJ38373 fis, clone FEBRA2002527
Homo sapiens cDNA FLJ38373 fis, clone FEBRA2002527gi|21755007|dbj|AK095692.1|Nucleotide
-
DENN/MADD domain containing 3, isoform CRA_e [Homo sapiens]
DENN/MADD domain containing 3, isoform CRA_e [Homo sapiens]gi|119612626|gb|EAW92220.1||gnl|WGS |hCP1916603Protein
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024