NM_000138.5(FBN1):c.*867G>T AND Stiff skin syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000398682.5
Allele description [Variation Report for NM_000138.5(FBN1):c.*867G>T]
NM_000138.5(FBN1):c.*867G>T
Condition(s)
-
Rattus norvegicus G protein-coupled receptor associated sorting protein 2 (Gpras...
Rattus norvegicus G protein-coupled receptor associated sorting protein 2 (Gprasp2), transcript variant 1, mRNAgi|2188194518|ref|NM_001401157.1|Nucleotide
-
Homo sapiens nuclear receptor binding protein 2, mRNA (cDNA clone IMAGE:4375917)
Homo sapiens nuclear receptor binding protein 2, mRNA (cDNA clone IMAGE:4375917)gi|48735259|gb|BC071605.1|Nucleotide
-
Homo sapiens nuclear receptor binding protein 2, mRNA (cDNA clone IMAGE:5180619)...
Homo sapiens nuclear receptor binding protein 2, mRNA (cDNA clone IMAGE:5180619), with apparent retained introngi|23337035|gb|BC037396.1|Nucleotide
-
Homo sapiens chromosome 11 open reading frame 66, mRNA (cDNA clone MGC:61781 IMA...
Homo sapiens chromosome 11 open reading frame 66, mRNA (cDNA clone MGC:61781 IMAGE:5166383), complete cdsgi|32449814|gb|BC053995.1|Nucleotide
-
PREDICTED: Homo sapiens CREB/ATF bZIP transcription factor (CREBZF), transcript ...
PREDICTED: Homo sapiens CREB/ATF bZIP transcription factor (CREBZF), transcript variant X2, mRNAgi|2462526808|ref|XM_054369569.1|Nucleotide
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Last Updated: Mar 30, 2024