NM_004646.4(NPHS1):c.1012+68A>G AND Finnish congenital nephrotic syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 17, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001827545.1
Allele description [Variation Report for NM_004646.4(NPHS1):c.1012+68A>G]
NM_004646.4(NPHS1):c.1012+68A>G
Condition(s)
-
Rattus norvegicus MLLT1, super elongation complex subunit (Mllt1), mRNA
Rattus norvegicus MLLT1, super elongation complex subunit (Mllt1), mRNAgi|1937877801|ref|NM_001106876.2|Nucleotide
-
SRX4823396 (1)
SRA
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024