NM_001177316.2(SLC34A3):c.942G>C (p.Ala314=) AND Autosomal recessive hypophosphatemic bone disease
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Sep 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002495828.2
Allele description [Variation Report for NM_001177316.2(SLC34A3):c.942G>C (p.Ala314=)]
NM_001177316.2(SLC34A3):c.942G>C (p.Ala314=)
Condition(s)
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thiolase family protein [Gordonia amarae]
thiolase family protein [Gordonia amarae]gi|1799596370|gnl|PRJNA587209|GII34 0|gb|QHN23495.1|Protein
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PREDICTED: Homo sapiens colony stimulating factor 2 receptor subunit alpha (CSF2...
PREDICTED: Homo sapiens colony stimulating factor 2 receptor subunit alpha (CSF2RA), transcript variant X9, mRNAgi|2217391108|ref|XM_011546174.4|Nucleotide
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PREDICTED: Homo sapiens colony stimulating factor 2 receptor subunit alpha (CSF2...
PREDICTED: Homo sapiens colony stimulating factor 2 receptor subunit alpha (CSF2RA), transcript variant X1, mRNAgi|2462631884|ref|XM_054328241.1|Nucleotide
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Taxonomy Links for Nucleotide (Select 2462583397) (1)
Taxonomy
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See more...Assertion and evidence details
Last Updated: Feb 28, 2024