NM_000428.3(LTBP2):c.5337T>A (p.Asp1779Glu) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004069030.1
Allele description [Variation Report for NM_000428.3(LTBP2):c.5337T>A (p.Asp1779Glu)]
NM_000428.3(LTBP2):c.5337T>A (p.Asp1779Glu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Thioclava sp. IC9 contig4, whole genome shotgun sequence
Thioclava sp. IC9 contig4, whole genome shotgun sequencegi|1213661261|gb|NBNX01000004.1||gn :NBNX01|contig4Nucleotide
-
Mus musculus fermitin family member 2 (Fermt2), transcript variant 3, mRNA
Mus musculus fermitin family member 2 (Fermt2), transcript variant 3, mRNAgi|2623980719|ref|NM_146054.4|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024