NM_005477.3(HCN4):c.531C>T (p.Ala177=) AND Brugada syndrome 8
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001495024.7
Allele description [Variation Report for NM_005477.3(HCN4):c.531C>T (p.Ala177=)]
NM_005477.3(HCN4):c.531C>T (p.Ala177=)
Condition(s)
-
Homo sapiens small proline-rich protein 2B (SPRR2B) gene, complete cds
Homo sapiens small proline-rich protein 2B (SPRR2B) gene, complete cdsgi|14599483|gb|AF333952.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024