NM_000455.5(STK11):c.1221G>C (p.Glu407Asp) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000774151.4
Allele description [Variation Report for NM_000455.5(STK11):c.1221G>C (p.Glu407Asp)]
NM_000455.5(STK11):c.1221G>C (p.Glu407Asp)
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
-
mitochondrial arginine transporter BAC2 [Quercus suber]
mitochondrial arginine transporter BAC2 [Quercus suber]gi|1344063937|ref|XP_023915594.1|Protein
-
carboxy terminal-processing peptidase [Thalassomonas haliotis]
carboxy terminal-processing peptidase [Thalassomonas haliotis]gi|2445162992|gnl|PRJNA649149|H3N35 0|gb|WDE09783.1|Protein
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024