NM_000546.6(TP53):c.920-7T>G AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003585850.1
Allele description [Variation Report for NM_000546.6(TP53):c.920-7T>G]
NM_000546.6(TP53):c.920-7T>G
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
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Mus musculus mitogen-activated protein kinase 9 (Mapk9), transcript variant beta...
Mus musculus mitogen-activated protein kinase 9 (Mapk9), transcript variant beta1, mRNAgi|254750711|ref|NM_016961.3|Nucleotide
-
PREDICTED: Homo sapiens LIM and calponin homology domains 1 (LIMCH1), transcript...
PREDICTED: Homo sapiens LIM and calponin homology domains 1 (LIMCH1), transcript variant X18, mRNAgi|2217349543|ref|XM_017007898.2|Nucleotide
-
LIM and calponin homology domains-containing protein 1 isoform X24 [Homo sapiens...
LIM and calponin homology domains-containing protein 1 isoform X24 [Homo sapiens]gi|2462595711|ref|XP_054205280.1|Protein
-
Homo sapiens protein arginine methyltransferase 7 (PRMT7), transcript variant 12...
Homo sapiens protein arginine methyltransferase 7 (PRMT7), transcript variant 12, mRNAgi|1800417200|ref|NM_001378022.1|Nucleotide
-
PREDICTED: Homo sapiens protein arginine methyltransferase 7 (PRMT7), transcript...
PREDICTED: Homo sapiens protein arginine methyltransferase 7 (PRMT7), transcript variant X14, misc_RNAgi|2217306270|ref|XR_007064887.1|Nucleotide
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Last Updated: Sep 29, 2024