NM_001267550.2(TTN):c.79941A>G (p.Gln26647=) AND TTN-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 13, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004534932.2
Allele description [Variation Report for NM_001267550.2(TTN):c.79941A>G (p.Gln26647=)]
NM_001267550.2(TTN):c.79941A>G (p.Gln26647=)
Condition(s)
- Name:
- TTN-related disorder
- Synonyms:
- TTN-related condition; TTN-Related Disorders; TTN-related disease
- Identifiers:
-
Homo sapiens calcium/calmodulin-dependent protein kinase II inhibitor 2, mRNA (c...
Homo sapiens calcium/calmodulin-dependent protein kinase II inhibitor 2, mRNA (cDNA clone MGC:132737 IMAGE:8144080), complete cdsgi|85397542|gb|BC105077.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 20, 2024