NM_177438.3(DICER1):c.4899A>G (p.Val1633=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Sep 25, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000565025.4
Allele description [Variation Report for NM_177438.3(DICER1):c.4899A>G (p.Val1633=)]
NM_177438.3(DICER1):c.4899A>G (p.Val1633=)
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
-
mitogen-activated protein kinase kinase kinase kinase 5 isoform X4 [Homo sapiens...
mitogen-activated protein kinase kinase kinase kinase 5 isoform X4 [Homo sapiens]gi|2217296175|ref|XP_047286851.1|Protein
-
mitogen-activated protein kinase kinase kinase kinase 5 isoform X3 [Homo sapiens...
mitogen-activated protein kinase kinase kinase kinase 5 isoform X3 [Homo sapiens]gi|2462538677|ref|XP_054231277.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024