NM_001042492.3(NF1):c.6708T>C (p.Phe2236=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 24, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002368462.2
Allele description [Variation Report for NM_001042492.3(NF1):c.6708T>C (p.Phe2236=)]
NM_001042492.3(NF1):c.6708T>C (p.Phe2236=)
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
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
-
numb, isoform B [Drosophila melanogaster]
numb, isoform B [Drosophila melanogaster]gi|24583045|ref|NP_723460.1|Protein
-
4-hydroxybenzoyl-CoA thioesterase [Pseudomonas silesiensis]
4-hydroxybenzoyl-CoA thioesterase [Pseudomonas silesiensis]gi|1035885827|gnl|PRJNA315635|PMA3_ |gb|ANJ58801.1|Protein
-
OAS1 [Eptesicus fuscus]
OAS1 [Eptesicus fuscus]Gene ID:103287239Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024