NM_000428.3(LTBP2):c.3004C>G (p.Arg1002Gly) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 20, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004640212.1
Allele description [Variation Report for NM_000428.3(LTBP2):c.3004C>G (p.Arg1002Gly)]
NM_000428.3(LTBP2):c.3004C>G (p.Arg1002Gly)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Tssr111650 AND (alive[prop]) (0)
Gene
-
Eremichthys acros isolate EA13007 S7 ribosomal protein gene, intron 1
Eremichthys acros isolate EA13007 S7 ribosomal protein gene, intron 1gi|442560169|gb|JX443313.1|Nucleotide
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Siphateles bicolor isolate SE635 S7 ribosomal protein gene, intron 1
Siphateles bicolor isolate SE635 S7 ribosomal protein gene, intron 1gi|442560161|gb|JX443305.1|Nucleotide
-
ha04d11.x1 NCI_CGAP_Kid12 Homo sapiens cDNA clone IMAGE:2872725 3', mRNA sequenc...
ha04d11.x1 NCI_CGAP_Kid12 Homo sapiens cDNA clone IMAGE:2872725 3', mRNA sequencegi|7037011|gnl|dbEST|3877778|gb|AW4 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Aug 11, 2024