NM_001267550.2(TTN):c.104347C>T (p.Leu34783Phe) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Mar 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001572757.11
Allele description [Variation Report for NM_001267550.2(TTN):c.104347C>T (p.Leu34783Phe)]
NM_001267550.2(TTN):c.104347C>T (p.Leu34783Phe)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens isolate CHM13 chromosome 16, alternate assembly T2T-CHM13v2.0
Homo sapiens isolate CHM13 chromosome 16, alternate assembly T2T-CHM13v2.0gi|2194972954|gnl|ASM:GCF_009914825 ef|NC_060940.1||gpp|GPC_000012755.1||gnl|NCBI_GENOMES|119576Nucleotide
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See more...Assertion and evidence details
Last Updated: Aug 18, 2024