NM_198253.3(TERT):c.1002C>T (p.Ser334=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 12, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003188222.1
Allele description
NM_198253.3(TERT):c.1002C>T (p.Ser334=)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
opsin-5 isoform X1 [Rattus norvegicus]
opsin-5 isoform X1 [Rattus norvegicus]gi|1958802281|ref|XP_038939470.1|Protein
-
Bactrocera correcta voucher UHIM.ms05672 cytochrome oxidase subunit 1 (COI) gene...
Bactrocera correcta voucher UHIM.ms05672 cytochrome oxidase subunit 1 (COI) gene, partial cds; mitochondrialgi|2755093239|gnl|uoguelph|DACIN577 COI-5P|gb|PP571459.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023