NM_000179.3(MSH6):c.3307T>G (p.Phe1103Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jul 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000582599.6
Allele description [Variation Report for NM_000179.3(MSH6):c.3307T>G (p.Phe1103Val)]
NM_000179.3(MSH6):c.3307T>G (p.Phe1103Val)
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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alpha/beta-Hydrolases superfamily protein [Arabidopsis thaliana]
alpha/beta-Hydrolases superfamily protein [Arabidopsis thaliana]gi|42567922|ref|NP_197280.2|Protein
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Scedosporium apiospermum Linoleate 8R-lipoxygenase (SAPIO_CDS8083), partial mRNA
Scedosporium apiospermum Linoleate 8R-lipoxygenase (SAPIO_CDS8083), partial mRNAgi|1027069843|ref|XM_016789794.1|Nucleotide
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Homo sapiens ribonuclease T2, mRNA (cDNA clone MGC:47703 IMAGE:5225327), complet...
Homo sapiens ribonuclease T2, mRNA (cDNA clone MGC:47703 IMAGE:5225327), complete cdsgi|24981025|gb|BC039713.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024