NM_000314.4(PTEN):c.-1256G>A AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 24, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000129402.13
Allele description [Variation Report for NM_000314.4(PTEN):c.-1256G>A]
NM_000314.4(PTEN):c.-1256G>A
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
-
RecName: Full=Interferon-inducible protein AIM2; AltName: Full=Interferon-induci...
RecName: Full=Interferon-inducible protein AIM2; AltName: Full=Interferon-inducible protein 210; Short=Ifi-210; AltName: Full=Interferon-inducible protein p210gi|189027645|sp|Q91VJ1.2|AIM2_MOUSEProtein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 20, 2024