NM_014000.3(VCL):c.788C>G (p.Thr263Ser) AND Cardiovascular phenotype
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002418688.2
Allele description [Variation Report for NM_014000.3(VCL):c.788C>G (p.Thr263Ser)]
NM_014000.3(VCL):c.788C>G (p.Thr263Ser)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
-
Homo sapiens cAMP/cGMP phosphodiesterase 11A2 mRNA, complete cds, alternatively ...
Homo sapiens cAMP/cGMP phosphodiesterase 11A2 mRNA, complete cds, alternatively splicedgi|11141610|gb|AF281865.1|Nucleotide
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Last Updated: May 7, 2024