NM_001372053.1(ANKRD31):c.1694A>G (p.Asn565Ser) AND ANKRD31-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 11, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003918970.1
Allele description [Variation Report for NM_001372053.1(ANKRD31):c.1694A>G (p.Asn565Ser)]
NM_001372053.1(ANKRD31):c.1694A>G (p.Asn565Ser)
Condition(s)
- Name:
- ANKRD31-related disorder
- Synonyms:
- ANKRD31-related condition
- Identifiers:
-
calcium/calmodulin-dependent protein kinase type 1 isoform X4 [Homo sapiens]
calcium/calmodulin-dependent protein kinase type 1 isoform X4 [Homo sapiens]gi|2217346526|ref|XP_047305045.1|Protein
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See more...Assertion and evidence details
Last Updated: Jul 15, 2024