NM_001276345.2(TNNT2):c.391G>C (p.Val131Leu) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001244808.7
Allele description [Variation Report for NM_001276345.2(TNNT2):c.391G>C (p.Val131Leu)]
NM_001276345.2(TNNT2):c.391G>C (p.Val131Leu)
Condition(s)
- Name:
- Hypertrophic cardiomyopathy 2
- Synonyms:
- Familial hypertrophic cardiomyopathy 2; TNNT2-Related Familial Hypertrophic Cardiomyopathy
- Identifiers:
- MONDO: MONDO:0007266; MedGen: C1861864; OMIM: 115195
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Pseudomonas sp. HPC483 16S ribosomal RNA gene, partial sequence
Pseudomonas sp. HPC483 16S ribosomal RNA gene, partial sequencegi|62869576|gb|AY999037.1|Nucleotide
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Stenotrophomonas sp. HPC482 16S ribosomal RNA gene, partial sequence
Stenotrophomonas sp. HPC482 16S ribosomal RNA gene, partial sequencegi|62869575|gb|AY999036.1|Nucleotide
-
Staphylococcus sp. HPC480 16S ribosomal RNA gene, partial sequence
Staphylococcus sp. HPC480 16S ribosomal RNA gene, partial sequencegi|62869573|gb|AY999034.1|Nucleotide
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Last Updated: Sep 29, 2024