NM_198253.3(TERT):c.1461C>T (p.Phe487=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002396741.1
Allele description
NM_198253.3(TERT):c.1461C>T (p.Phe487=)
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
-
Homo sapiens exocyst complex component 1 (EXOC1), transcript variant 1, mRNA
Homo sapiens exocyst complex component 1 (EXOC1), transcript variant 1, mRNAgi|1890284661|ref|NM_018261.4|Nucleotide
-
RASAL3 [Chlorocebus sabaeus]
RASAL3 [Chlorocebus sabaeus]Gene ID:103234074Gene
-
GSE116090[ACCN] AND gsm[ETYP] (7)
GEO DataSets
-
m6A-seq map of wild type P6497 and methyltransferase knockout mutant of Phytopht...
m6A-seq map of wild type P6497 and methyltransferase knockout mutant of Phytophthora sojaeAccession: GSE221689GEO DataSets
-
GPL32987[RGSE] (1)
GEO DataSets
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Mar 5, 2024