NM_001451.3(FOXF1):c.46G>A (p.Gly16Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002798898.2
Allele description [Variation Report for NM_001451.3(FOXF1):c.46G>A (p.Gly16Ser)]
NM_001451.3(FOXF1):c.46G>A (p.Gly16Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
cAMP-responsive element modulator isoform X25 [Rattus norvegicus]
cAMP-responsive element modulator isoform X25 [Rattus norvegicus]gi|2678905919|ref|XP_063132169.1|Protein
-
NADH dehydrogenase subunit 4 (mitochondrion) [Pitambara triremiprocta]
NADH dehydrogenase subunit 4 (mitochondrion) [Pitambara triremiprocta]gi|2627915450|ref|YP_010990677.1|Protein
-
SAMN40588716 (1)
SRA
-
Tssr112206 AND (alive[prop]) (0)
Gene
-
Parkia biglandulosa trnL gene and trnL-trnF intergenic spacer, partial sequences...
Parkia biglandulosa trnL gene and trnL-trnF intergenic spacer, partial sequences; chloroplast genes for chloroplast productsgi|21541306|gb|AF278498.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024