NM_000249.4(MLH1):c.9C>G (p.Phe3Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- May 2, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000165278.9
Allele description [Variation Report for NM_000249.4(MLH1):c.9C>G (p.Phe3Leu)]
NM_000249.4(MLH1):c.9C>G (p.Phe3Leu)
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
-
Synaptobrevin family protein [Arabidopsis thaliana]
Synaptobrevin family protein [Arabidopsis thaliana]gi|15242973|ref|NP_200626.1|Protein
-
RecName: Full=Decapping and exoribonuclease protein; Short=DXO; AltName: Full=5'...
RecName: Full=Decapping and exoribonuclease protein; Short=DXO; AltName: Full=5'-3' exoribonuclease DXO; AltName: Full=Dom-3 homolog Z; AltName: Full=NAD-capped RNA hydrolase DXO; Short=DeNADding enzyme DXOgi|115311709|sp|O77932.2|DXO_HUMANProtein
-
Amyotrophic lateral sclerosis type 11
Amyotrophic lateral sclerosis type 11MedGen
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024