NM_000363.5(TNNI3):c.466C>G (p.Gln156Glu) AND Cardiomyopathy, familial restrictive, 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001134897.4
Allele description [Variation Report for NM_000363.5(TNNI3):c.466C>G (p.Gln156Glu)]
NM_000363.5(TNNI3):c.466C>G (p.Gln156Glu)
Condition(s)
-
Homo sapiens genomic DNA, chromosome 11 clone:RP11-159N11, complete sequence
Homo sapiens genomic DNA, chromosome 11 clone:RP11-159N11, complete sequencegi|40736960|dbj|AP002840.3|Nucleotide
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Last Updated: Apr 9, 2023