NM_006969.5(ZNF28):c.1950C>T (p.Leu650=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jun 19, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000894342.4
Allele description [Variation Report for NM_006969.5(ZNF28):c.1950C>T (p.Leu650=)]
NM_006969.5(ZNF28):c.1950C>T (p.Leu650=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PREDICTED: Homo sapiens PRAME family member 8 (PRAMEF8), transcript variant X1, ...
PREDICTED: Homo sapiens PRAME family member 8 (PRAMEF8), transcript variant X1, mRNAgi|2462496115|ref|XM_054331859.1|Nucleotide
-
DB031118 TESTI2 Homo sapiens cDNA clone TESTI2014979 5', mRNA sequence
DB031118 TESTI2 Homo sapiens cDNA clone TESTI2014979 5', mRNA sequencegi|82416772|gnl|dbEST|33854708|dbj| 118.1|Nucleotide
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Last Updated: Sep 29, 2024