NM_005529.7(HSPG2):c.4903G>A (p.Gly1635Arg) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002522113.2
Allele description [Variation Report for NM_005529.7(HSPG2):c.4903G>A (p.Gly1635Arg)]
NM_005529.7(HSPG2):c.4903G>A (p.Gly1635Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 30, 2024