NM_006580.4(CLDN16):c.-41G>T AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003294520.2
Allele description [Variation Report for NM_006580.4(CLDN16):c.-41G>T]
NM_006580.4(CLDN16):c.-41G>T
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens transforming growth factor beta 1 induced transcript 1, mRNA (cDNA ...
Homo sapiens transforming growth factor beta 1 induced transcript 1, mRNA (cDNA clone MGC:45093 IMAGE:5535913), complete cdsgi|21619704|gb|BC032545.1|Nucleotide
-
E011859-024-003-E16-SP6 MPIZ-ADIS-024-inflorescence Beta vulgaris cDNA clone 024...
E011859-024-003-E16-SP6 MPIZ-ADIS-024-inflorescence Beta vulgaris cDNA clone 024-003-E16 5-PRIME, mRNA sequencegi|26114001|gnl|dbEST|12698201|gb|B 24.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024