NM_002528.7(NTHL1):c.139G>A (p.Val47Met) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Mar 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002255529.5
Allele description [Variation Report for NM_002528.7(NTHL1):c.139G>A (p.Val47Met)]
NM_002528.7(NTHL1):c.139G>A (p.Val47Met)
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
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Armillaria gallica strain FOD8_21 large subunit ribosomal RNA gene and intergeni...
Armillaria gallica strain FOD8_21 large subunit ribosomal RNA gene and intergenic spacer 1, partial sequencegi|1128693950|gb|KX618609.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024