NM_001394073.1(HS6ST2):c.1045C>T (p.Arg349Trp) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004404394.1
Allele description [Variation Report for NM_001394073.1(HS6ST2):c.1045C>T (p.Arg349Trp)]
NM_001394073.1(HS6ST2):c.1045C>T (p.Arg349Trp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024