NM_022087.4(GALNT11):c.451C>T (p.Pro151Ser) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Sep 11, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000961836.4
Allele description [Variation Report for NM_022087.4(GALNT11):c.451C>T (p.Pro151Ser)]
NM_022087.4(GALNT11):c.451C>T (p.Pro151Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024