NM_024577.4(SH3TC2):c.2087A>G (p.His696Arg) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Mar 4, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000205788.19
Allele description [Variation Report for NM_024577.4(SH3TC2):c.2087A>G (p.His696Arg)]
NM_024577.4(SH3TC2):c.2087A>G (p.His696Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 20, 2024