NM_004787.4(SLIT2):c.1190A>G (p.Asn397Ser) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 20, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000982220.3
Allele description [Variation Report for NM_004787.4(SLIT2):c.1190A>G (p.Asn397Ser)]
NM_004787.4(SLIT2):c.1190A>G (p.Asn397Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Feb 7, 2023