NM_020066.5(FMN2):c.1591G>T (p.Asp531Tyr) AND Intellectual disability, autosomal recessive 47
- Germline classification:
- not provided (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003988647.2
Allele description [Variation Report for NM_020066.5(FMN2):c.1591G>T (p.Asp531Tyr)]
NM_020066.5(FMN2):c.1591G>T (p.Asp531Tyr)
Condition(s)
-
Homo sapiens RAB, member of RAS oncogene family like 2A (RABL2A), transcript var...
Homo sapiens RAB, member of RAS oncogene family like 2A (RABL2A), transcript variant 28, non-coding RNAgi|1700447856|ref|NR_148880.2|Nucleotide
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Microbacterium resistens strain SCK_457 16S ribosomal RNA gene, partial sequence
Microbacterium resistens strain SCK_457 16S ribosomal RNA gene, partial sequencegi|2805779772|gb|PQ344097.1|Nucleotide
-
Microbacterium resistens strain Y8 16S ribosomal RNA gene, partial sequence
Microbacterium resistens strain Y8 16S ribosomal RNA gene, partial sequencegi|2808867660|gb|PQ363168.1|Nucleotide
-
SNR17B [Saccharomyces cerevisiae S288C]
SNR17B [Saccharomyces cerevisiae S288C]Gene ID:9164985Gene
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Last Updated: Jun 23, 2024