NM_001130987.2(DYSF):c.3958T>C (p.Ser1320Pro) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 17, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002516759.2
Allele description [Variation Report for NM_001130987.2(DYSF):c.3958T>C (p.Ser1320Pro)]
NM_001130987.2(DYSF):c.3958T>C (p.Ser1320Pro)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Mus musculus POU domain, class 3, transcription factor 4 (Pou3f4), mRNA
Mus musculus POU domain, class 3, transcription factor 4 (Pou3f4), mRNAgi|922304280|ref|NM_008901.2|Nucleotide
-
Endopterygota sp. NZAC 03011444 voucher NZAC:03011444 28S ribosomal RNA gene, pa...
Endopterygota sp. NZAC 03011444 voucher NZAC:03011444 28S ribosomal RNA gene, partial sequencegi|983653734|gb|KT440543.1|Nucleotide
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Last Updated: May 1, 2024