NM_000308.4(CTSA):c.33GCT[7] (p.Leu19del) AND not provided
- Germline classification:
- Benign (4 submissions)
- Last evaluated:
- Jun 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000588925.11
Allele description [Variation Report for NM_000308.4(CTSA):c.33GCT[7] (p.Leu19del)]
NM_000308.4(CTSA):c.33GCT[7] (p.Leu19del)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Petrocephalus soudanensis rhodopsin (RH1) mRNA, partial cds
Petrocephalus soudanensis rhodopsin (RH1) mRNA, partial cdsgi|1401664165|gb|KY982944.1|Nucleotide
-
Acidithiobacillus caldus strain CV18-1 Contig80, whole genome shotgun sequence
Acidithiobacillus caldus strain CV18-1 Contig80, whole genome shotgun sequencegi|2052356408|ref|NZ_JAAOMS01000008 gnl|WGS:NZ_JAAOMS01|Contig80Nucleotide
-
Acidithiobacillus caldus strain ZJ Contig181, whole genome shotgun sequence
Acidithiobacillus caldus strain ZJ Contig181, whole genome shotgun sequencegi|1079310461|ref|NZ_LZYG01000181.1 |WGS:NZ_LZYG01|Contig181Nucleotide
-
PREDICTED: Homo sapiens zinc finger and SCAN domain containing 32 (ZSCAN32), tra...
PREDICTED: Homo sapiens zinc finger and SCAN domain containing 32 (ZSCAN32), transcript variant X7, mRNAgi|2462549532|ref|XM_054380581.1|Nucleotide
-
Homo sapiens zinc finger and SCAN domain containing 32 (ZSCAN32), transcript var...
Homo sapiens zinc finger and SCAN domain containing 32 (ZSCAN32), transcript variant 4, mRNAgi|1676319234|ref|NM_001284529.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Flagged submissions
Submission Accession | Submitter | Review Status (Assertion method) | Clinical Significance (Last evaluated) | Origin | Method | Citations |
---|---|---|---|---|---|---|
SCV000696509 | Women's Health and Genetics/Laboratory Corporation of America, LabCorp | flagged submission Reason: This record appears to be redundant with a more recent record from the same submitter. Notes: SCV000696509 appears to be redundant with SCV003928935. (LabCorp Variant Classification Summary - May 2015) | Benign (Nov 22, 2017) | germline | clinical testing | PubMed (1) LabCorp Variant Classification Summary - May 2015.docx |
Last Updated: Sep 29, 2024