NM_000546.6(TP53):c.205del (p.Ala69fs) AND Li-Fraumeni syndrome
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Sep 23, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001382613.5
Allele description [Variation Report for NM_000546.6(TP53):c.205del (p.Ala69fs)]
NM_000546.6(TP53):c.205del (p.Ala69fs)
Condition(s)
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PREDICTED: Homo sapiens hydroxysteroid dehydrogenase like 1 (HSDL1), transcript ...
PREDICTED: Homo sapiens hydroxysteroid dehydrogenase like 1 (HSDL1), transcript variant X1, mRNAgi|2462551116|ref|XM_054314092.1|Nucleotide
-
PREDICTED: Ovis aries LYR motif containing 9 (LYRM9), transcript variant X15, mR...
PREDICTED: Ovis aries LYR motif containing 9 (LYRM9), transcript variant X15, mRNAgi|2606997800|ref|XM_060395281.1|Nucleotide
-
PREDICTED: Ovis aries LYR motif containing 9 (LYRM9), transcript variant X18, mi...
PREDICTED: Ovis aries LYR motif containing 9 (LYRM9), transcript variant X18, misc_RNAgi|2606997803|ref|XR_009595504.1|Nucleotide
-
Vicia subvillosa isolate HV23 ribulose-1,5-bisphosphate carboxylase/oxygenase la...
Vicia subvillosa isolate HV23 ribulose-1,5-bisphosphate carboxylase/oxygenase large subunit (rbcL) gene, partial cds; chloroplastgi|440233695|gb|JX505518.1|Nucleotide
-
Homo sapiens chromosome 8, GRCh38.p14 Primary Assembly
Homo sapiens chromosome 8, GRCh38.p14 Primary Assemblygi|568815590|gnl|ASM:GCF_000001305| |NC_000008.11||gpp|GPC_000001300.1||gnl|NCBI_GENOMES|8Nucleotide
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Last Updated: Sep 29, 2024