NM_020975.6(RET):c.332T>G (p.Val111Gly) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 11, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002326483.2
Allele description [Variation Report for NM_020975.6(RET):c.332T>G (p.Val111Gly)]
NM_020975.6(RET):c.332T>G (p.Val111Gly)
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
-
synaptic vesicle membrane protein VAT-1 homolog-like [Mus musculus]
synaptic vesicle membrane protein VAT-1 homolog-like [Mus musculus]gi|33667095|ref|NP_766604.2|Protein
-
PREDICTED: Cucurbita maxima peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine ...
PREDICTED: Cucurbita maxima peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase (LOC111465478), mRNAgi|1281047198|ref|XM_023109872.1|Nucleotide
-
cytochrome oxidase subunit 1, partial (mitochondrion) [Mymaridae sp. CNFNT1467-1...
cytochrome oxidase subunit 1, partial (mitochondrion) [Mymaridae sp. CNFNT1467-14]gi|998442623|gb|AMK41268.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024