NM_174916.3(UBR1):c.4104C>G (p.Thr1368=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003858770.2
Allele description [Variation Report for NM_174916.3(UBR1):c.4104C>G (p.Thr1368=)]
NM_174916.3(UBR1):c.4104C>G (p.Thr1368=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens phosphoprotein ULIP6 (ULIP6) mRNA, complete cds
Homo sapiens phosphoprotein ULIP6 (ULIP6) mRNA, complete cdsgi|13259168|gb|AF264015.1|Nucleotide
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PREDICTED: Homo sapiens PCI domain containing 2 (PCID2), transcript variant X9, ...
PREDICTED: Homo sapiens PCI domain containing 2 (PCID2), transcript variant X9, mRNAgi|2462537529|ref|XM_054374749.1|Nucleotide
-
Homo sapiens homeotic protein HB9 gene, partial cds
Homo sapiens homeotic protein HB9 gene, partial cdsgi|342160297|gb|AH007909.2|SEG_HSHBNucleotide
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Last Updated: Sep 29, 2024