NM_002528.7(NTHL1):c.186C>G (p.Gly62=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 31, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002421137.2
Allele description [Variation Report for NM_002528.7(NTHL1):c.186C>G (p.Gly62=)]
NM_002528.7(NTHL1):c.186C>G (p.Gly62=)
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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BJ078410 NIBB Mochii normalized Xenopus tailbud library Xenopus laevis cDNA clon...
BJ078410 NIBB Mochii normalized Xenopus tailbud library Xenopus laevis cDNA clone XL065b01 3', mRNA sequencegi|17523326|gnl|dbEST|10542719|dbj| 410.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024