NM_001325.3(CSTF2):c.147C>T (p.Tyr49=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 8, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000921726.3
Allele description [Variation Report for NM_001325.3(CSTF2):c.147C>T (p.Tyr49=)]
NM_001325.3(CSTF2):c.147C>T (p.Tyr49=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
eggcsite.comUCt (0)
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Last Updated: Aug 23, 2022