GRCh37/hg19 1p31.1(chr1:79113712-79189810)x1 AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 25, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001259069.1
Allele description [Variation Report for GRCh37/hg19 1p31.1(chr1:79113712-79189810)x1]
GRCh37/hg19 1p31.1(chr1:79113712-79189810)x1
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
Homo sapiens U6 snRNA biogenesis phosphodiesterase 1 (USB1), transcript variant ...
Homo sapiens U6 snRNA biogenesis phosphodiesterase 1 (USB1), transcript variant 4, mRNAgi|1677501500|ref|NM_001330568.2|Nucleotide
-
Homo sapiens involucrin (IVL), mRNA
Homo sapiens involucrin (IVL), mRNAgi|1914825640|ref|NM_005547.4|Nucleotide
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Last Updated: Apr 23, 2022