NM_000363.5(TNNI3):c.273G>A (p.Ala91=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 25, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002433496.1
Allele description
NM_000363.5(TNNI3):c.273G>A (p.Ala91=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
-
Homo sapiens isolate CHM13 chromosome 7, alternate assembly T2T-CHM13v2.0
Homo sapiens isolate CHM13 chromosome 7, alternate assembly T2T-CHM13v2.0gi|2194973865|gnl|ASM:GCF_009914825 f|NC_060931.1||gpp|GPC_000012746.1||gnl|NCBI_GENOMES|119567Nucleotide
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See more...Assertion and evidence details
Last Updated: Apr 20, 2024