NM_001042492.3(NF1):c.7067C>T (p.Pro2356Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 15, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000562473.1
Allele description [Variation Report for NM_001042492.3(NF1):c.7067C>T (p.Pro2356Leu)]
NM_001042492.3(NF1):c.7067C>T (p.Pro2356Leu)
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
-
UL8 [Papiine alphaherpesvirus 2]
UL8 [Papiine alphaherpesvirus 2]Gene ID:3850240Gene
-
JGI_CABH8769.fwd NIH_XGC_tropSkeMus1 Xenopus tropicalis cDNA clone IMAGE:7851564...
JGI_CABH8769.fwd NIH_XGC_tropSkeMus1 Xenopus tropicalis cDNA clone IMAGE:7851564 5', mRNA sequencegi|73777611|gnl|dbEST|31032826|gb|D 14.1|Nucleotide
-
Homo sapiens
Homo sapiensPilot ENCODE transcriptome dataBioProject
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023