NM_025132.4(WDR19):c.3502G>A (p.Asp1168Asn) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 11, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002568534.2
Allele description [Variation Report for NM_025132.4(WDR19):c.3502G>A (p.Asp1168Asn)]
NM_025132.4(WDR19):c.3502G>A (p.Asp1168Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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Taxonomy Links for Protein (Select 383397238) (1)
Taxonomy
-
Protein Links for Nucleotide (Select 1281293929) (37)
Protein
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Homo sapiens USP6 N-terminal like (USP6NL), transcript variant 4, mRNA
Homo sapiens USP6 N-terminal like (USP6NL), transcript variant 4, mRNAgi|1959221270|ref|NM_001391959.1|Nucleotide
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Chromosome neighbors for GEO Profiles (Select 52823581) (18)
GEO Profiles
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Conservatibacter flavescens strain 7.4 contig41, whole genome shotgun sequence
Conservatibacter flavescens strain 7.4 contig41, whole genome shotgun sequencegi|1281293926|ref|NZ_PHHA01000041.1 |WGS:NZ_PHHA01|contig41Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024