NM_001177316.2(SLC34A3):c.688A>C (p.Thr230Pro) AND Autosomal recessive hypophosphatemic bone disease
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002505640.1
Allele description [Variation Report for NM_001177316.2(SLC34A3):c.688A>C (p.Thr230Pro)]
NM_001177316.2(SLC34A3):c.688A>C (p.Thr230Pro)
Condition(s)
-
zinc finger protein 760 isoform 1 [Mus musculus]
zinc finger protein 760 isoform 1 [Mus musculus]gi|2284291931|ref|NP_001397493.1|Protein
-
zinc finger protein 760 isoform X3 [Mus musculus]
zinc finger protein 760 isoform X3 [Mus musculus]gi|1907124299|ref|XP_036016484.1|Protein
-
abl interactor 1 isoform X4 [Homo sapiens]
abl interactor 1 isoform X4 [Homo sapiens]gi|2217275024|ref|XP_047280362.1|Protein
-
Homo sapiens solute carrier family 23 member 3 (SLC23A3), transcript variant 1, ...
Homo sapiens solute carrier family 23 member 3 (SLC23A3), transcript variant 1, mRNAgi|1677501203|ref|NM_144712.5|Nucleotide
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Oryza sativa Japonica Group strain:Nipponbare
Oryza sativa Japonica Group strain:NipponbareInternational Rice Genome Sequencing ProjectBioProject
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See more...Assertion and evidence details
Last Updated: May 1, 2024