NM_000143.4(FH):c.1056T>C (p.Gly352=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 3, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002399904.9
Allele description [Variation Report for NM_000143.4(FH):c.1056T>C (p.Gly352=)]
NM_000143.4(FH):c.1056T>C (p.Gly352=)
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
-
2651910[uid] (1)
Taxonomy
-
Mus musculus targeted KO-first, conditional ready, lacZ-tagged mutant allele Syf...
Mus musculus targeted KO-first, conditional ready, lacZ-tagged mutant allele Syf2:tm1a(EUCOMM)Wtsi; transgenicgi|354781421|gb|JN945922.1|Nucleotide
-
190431[uid] (1)
Taxonomy
-
Brevundimonas sp. 8_2 partial 16S rRNA gene, strain 8_2
Brevundimonas sp. 8_2 partial 16S rRNA gene, strain 8_2gi|557675895|emb|HF954486.1|Nucleotide
-
240719[uid] (1)
Taxonomy
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024