NM_173582.6(PGM2L1):c.641A>G (p.Asn214Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 4, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004498725.1
Allele description [Variation Report for NM_173582.6(PGM2L1):c.641A>G (p.Asn214Ser)]
NM_173582.6(PGM2L1):c.641A>G (p.Asn214Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
ORF6 protein [Severe acute respiratory syndrome coronavirus 2]
ORF6 protein [Severe acute respiratory syndrome coronavirus 2]gi|2754671103|gb|XCM62860.1|Protein
-
ORF1ab polyprotein, partial [Severe acute respiratory syndrome coronavirus 2]
ORF1ab polyprotein, partial [Severe acute respiratory syndrome coronavirus 2]gi|2754671098|gb|XCM62855.1|Protein
-
ORF10 protein [Severe acute respiratory syndrome coronavirus 2]
ORF10 protein [Severe acute respiratory syndrome coronavirus 2]gi|2754671108|gb|XCM62865.1|Protein
-
RNA-dependent RNA polymerase, partial [Murine coronavirus]
RNA-dependent RNA polymerase, partial [Murine coronavirus]gi|2243704829|gb|URC20767.1|Protein
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Last Updated: May 7, 2024