NM_000548.5(TSC2):c.3674A>G (p.Asn1225Ser) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002456423.2
Allele description [Variation Report for NM_000548.5(TSC2):c.3674A>G (p.Asn1225Ser)]
NM_000548.5(TSC2):c.3674A>G (p.Asn1225Ser)
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
-
CD44 antigen isoform X1 [Rattus norvegicus]
CD44 antigen isoform X1 [Rattus norvegicus]gi|564342033|ref|XP_006234689.1|Protein
-
PREDICTED: Rattus norvegicus Cd44 molecule (Cd44), transcript variant X7, mRNA
PREDICTED: Rattus norvegicus Cd44 molecule (Cd44), transcript variant X7, mRNAgi|672046390|ref|XM_006234631.2|Nucleotide
-
PREDICTED: Rattus norvegicus Cd44 molecule (Cd44), transcript variant X6, mRNA
PREDICTED: Rattus norvegicus Cd44 molecule (Cd44), transcript variant X6, mRNAgi|672046388|ref|XM_008762058.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024