NM_000392.5(ABCC2):c.3867G>T (p.Arg1289Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004419928.1
Allele description [Variation Report for NM_000392.5(ABCC2):c.3867G>T (p.Arg1289Ser)]
NM_000392.5(ABCC2):c.3867G>T (p.Arg1289Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Ophidion asiro isolate ASIZP_0910637 NADH dehydrogenase subunit 4 (ND4) gene, pa...
Ophidion asiro isolate ASIZP_0910637 NADH dehydrogenase subunit 4 (ND4) gene, partial cds; tRNA-His gene, complete sequence; and tRNA-Ser gene, partial sequence; mitochondrialgi|2789066575|gb|OR818727.1|Nucleotide
-
spindlin-1 isoform 2 [Mus musculus]
spindlin-1 isoform 2 [Mus musculus]gi|22165378|ref|NP_666155.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 7, 2024