NM_000552.5(VWF):c.5694G>C (p.Gln1898His) AND von Willebrand disease type 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 28, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001420488.2
Allele description [Variation Report for NM_000552.5(VWF):c.5694G>C (p.Gln1898His)]
NM_000552.5(VWF):c.5694G>C (p.Gln1898His)
Condition(s)
-
Homo sapiens isolate:CHM13
Homo sapiens isolate:CHM13Homo sapiens isolate:CHM13 RefSeq Genome sequencing and assemblyBioProject
-
Bacteria 16S ribosomal RNA gene, partial sequence.
Bacteria 16S ribosomal RNA gene, partial sequence.PopSet: 5031307PopSet
-
txid95842[Organism:noexp] (1)
PopSet
-
BioProject Links for Protein (Select 2462567481) (1)
BioProject
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2023