NM_000051.4(ATM):c.994T>G (p.Tyr332Asp) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 5, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002382926.2
Allele description [Variation Report for NM_000051.4(ATM):c.994T>G (p.Tyr332Asp)]
NM_000051.4(ATM):c.994T>G (p.Tyr332Asp)
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
-
aspartyl/asparaginyl beta-hydroxylase isoform X1 [Theropithecus gelada]
aspartyl/asparaginyl beta-hydroxylase isoform X1 [Theropithecus gelada]gi|1411172505|ref|XP_025248980.1|Protein
-
PREDICTED: prolyl 3-hydroxylase 2 isoform X3 [Capra hircus]
PREDICTED: prolyl 3-hydroxylase 2 isoform X3 [Capra hircus]gi|1062849558|ref|XP_005675181.3|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024