NM_001267550.2(TTN):c.107870T>C (p.Ile35957Thr) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002823980.2
Allele description [Variation Report for NM_001267550.2(TTN):c.107870T>C (p.Ile35957Thr)]
NM_001267550.2(TTN):c.107870T>C (p.Ile35957Thr)
Condition(s)
-
"Genomics Facility, Ludwig-Maximilians-Universitat Munchen"[submi... (1)
"Genomics Facility, Ludwig-Maximilians-Universitat Munchen"[submitter] AND "BTK"[gene]SearchClinVar
-
Genome Links for Gene (Select 100874185) (1)
Genome
-
dbVar for Gene (Select 116435278) (240)
dbVar
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Last Updated: Feb 28, 2024