NM_201596.3(CACNB2):c.1314T>C (p.Asp438=) AND Brugada syndrome 4
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 3, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001393930.14
Allele description [Variation Report for NM_201596.3(CACNB2):c.1314T>C (p.Asp438=)]
NM_201596.3(CACNB2):c.1314T>C (p.Asp438=)
Condition(s)
-
Homo sapiens neuroligin 4 Y-linked (NLGN4Y), transcript variant 2, mRNA
Homo sapiens neuroligin 4 Y-linked (NLGN4Y), transcript variant 2, mRNAgi|256222831|ref|NM_001164238.1|Nucleotide
-
17q21.1 (14)
OMIM
-
MINPP1 [Mustela putorius furo]
MINPP1 [Mustela putorius furo]Gene ID:101692752Gene
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Last Updated: Oct 13, 2024