NM_002292.4(LAMB2):c.4484T>A (p.Leu1495Gln) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002874306.2
Allele description [Variation Report for NM_002292.4(LAMB2):c.4484T>A (p.Leu1495Gln)]
NM_002292.4(LAMB2):c.4484T>A (p.Leu1495Gln)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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Methanotorris formicicus Mc-S-70 ctg177, whole genome shotgun sequence
Methanotorris formicicus Mc-S-70 ctg177, whole genome shotgun sequencegi|373561491|gb|AGJL01000012.1||gnl AGJL01|ctg177Nucleotide
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Methanotorris formicicus Mc-S-70 ctg187, whole genome shotgun sequence
Methanotorris formicicus Mc-S-70 ctg187, whole genome shotgun sequencegi|373563297|gb|AGJL01000002.1||gnl AGJL01|ctg187Nucleotide
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Methanotorris formicicus Mc-S-70 ctg188, whole genome shotgun sequence
Methanotorris formicicus Mc-S-70 ctg188, whole genome shotgun sequencegi|373563416|gb|AGJL01000001.1||gnl AGJL01|ctg188Nucleotide
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Methanotorris formicicus rrn gene for small subunit ribosomal RNA, partial seque...
Methanotorris formicicus rrn gene for small subunit ribosomal RNA, partial sequencegi|33284944|dbj|AB100884.1|Nucleotide
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7a22h11.x1 NCI_CGAP_GC6 Homo sapiens cDNA clone IMAGE:3219525 3', mRNA sequence
7a22h11.x1 NCI_CGAP_GC6 Homo sapiens cDNA clone IMAGE:3219525 3', mRNA sequencegi|9792076|gnl|dbEST|5758879|gb|BE5 .1|Nucleotide
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Last Updated: May 1, 2024