NM_007375.4(TARDBP):c.1054A>G (p.Asn352Asp) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004067954.1
Allele description [Variation Report for NM_007375.4(TARDBP):c.1054A>G (p.Asn352Asp)]
NM_007375.4(TARDBP):c.1054A>G (p.Asn352Asp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Burkholderia sp. BV56 16S ribosomal RNA gene, partial sequence
Burkholderia sp. BV56 16S ribosomal RNA gene, partial sequencegi|443254570|gb|KC255219.1|Nucleotide
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Homo sapiens histone cluster 1, H1d, mRNA (cDNA clone MGC:138176 IMAGE:8327439),...
Homo sapiens histone cluster 1, H1d, mRNA (cDNA clone MGC:138176 IMAGE:8327439), complete cdsgi|85566623|gb|BC111971.1|Nucleotide
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Last Updated: Sep 29, 2024