NM_030973.4(MED25):c.629C>T (p.Pro210Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002562458.2
Allele description [Variation Report for NM_030973.4(MED25):c.629C>T (p.Pro210Leu)]
NM_030973.4(MED25):c.629C>T (p.Pro210Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
DC396757 TESTI2 Homo sapiens cDNA clone TESTI2021825 5', mRNA sequence
DC396757 TESTI2 Homo sapiens cDNA clone TESTI2021825 5', mRNA sequencegi|146065735|gnl|dbEST|46558619|dbj 6757.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024