NM_000057.4(BLM):c.3098T>C (p.Ile1033Thr) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 24, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002323685.2
Allele description [Variation Report for NM_000057.4(BLM):c.3098T>C (p.Ile1033Thr)]
NM_000057.4(BLM):c.3098T>C (p.Ile1033Thr)
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
-
Polynucleobacter sp. AP-Titi-500A-B4 chromosome
Polynucleobacter sp. AP-Titi-500A-B4 chromosomegi|2047853639|gb|CP061311.1|Nucleotide
-
AU015791 expressed sequence AU015791 [Mus musculus]
AU015791 expressed sequence AU015791 [Mus musculus]Gene ID:104932Gene
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Last Updated: Sep 29, 2024