NM_000551.4(VHL):c.589G>A (p.Asp197Asn) AND Von Hippel-Lindau syndrome
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Aug 6, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002251697.1
Allele description [Variation Report for NM_000551.4(VHL):c.589G>A (p.Asp197Asn)]
NM_000551.4(VHL):c.589G>A (p.Asp197Asn)
Condition(s)
-
AGENCOURT_11210942 NICHD_XGC_Tad2 Xenopus laevis cDNA clone IMAGE:6873792 5', mR...
AGENCOURT_11210942 NICHD_XGC_Tad2 Xenopus laevis cDNA clone IMAGE:6873792 5', mRNA sequencegi|29135877|gnl|dbEST|17126448|gb|C 96.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023