NM_000099.4(CST3):c.168C>T (p.Ala56=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003740075.2
Allele description [Variation Report for NM_000099.4(CST3):c.168C>T (p.Ala56=)]
NM_000099.4(CST3):c.168C>T (p.Ala56=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Aspergillus lentulus uncharacterized protein (IFM58399_10438), partial mRNA
Aspergillus lentulus uncharacterized protein (IFM58399_10438), partial mRNAgi|1832836433|ref|XM_033564714.1|Nucleotide
-
unnamed protein product [Homo sapiens]
unnamed protein product [Homo sapiens]gi|194387076|dbj|BAG59904.1|Protein
-
Homo sapiens cell line PE/CA-PJ15 SCCA1/SCCA2 fusion protein mRNA, complete cds
Homo sapiens cell line PE/CA-PJ15 SCCA1/SCCA2 fusion protein mRNA, complete cdsgi|33313306|gb|AF428136.1|Nucleotide
-
LOC122152352 [Homo sapiens]
LOC122152352 [Homo sapiens]Gene ID:122152352Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024