NM_001684.5(ATP2B4):c.927T>C (p.Asn309=) AND ATP2B4-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 31, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003954349.1
Allele description [Variation Report for NM_001684.5(ATP2B4):c.927T>C (p.Asn309=)]
NM_001684.5(ATP2B4):c.927T>C (p.Asn309=)
Condition(s)
- Name:
- ATP2B4-related disorder
- Synonyms:
- ATP2B4-related condition
- Identifiers:
-
helix-turn-helix domain-containing protein [Fibrobacter sp.]
helix-turn-helix domain-containing protein [Fibrobacter sp.]gi|2769134793|ref|WP_366075231.1|Protein
-
Homo sapiens plastin 3 (PLS3), transcript variant 3, mRNA
Homo sapiens plastin 3 (PLS3), transcript variant 3, mRNAgi|1676324971|ref|NM_001172335.3|Nucleotide
-
Butyrivibrio sp. AE3003
Butyrivibrio sp. AE3003Butyrivibrio sp. AE3003 Genome sequencing and assemblyBioProject
-
Butyrivibrio sp. INlla16
Butyrivibrio sp. INlla16Butyrivibrio sp. INlla16 Genome sequencingBioProject
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See more...Assertion and evidence details
Last Updated: May 19, 2024