NM_001130823.3(DNMT1):c.3413C>G (p.Ser1138Cys) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 27, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000732184.4
Allele description [Variation Report for NM_001130823.3(DNMT1):c.3413C>G (p.Ser1138Cys)]
NM_001130823.3(DNMT1):c.3413C>G (p.Ser1138Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
100K [Human adenovirus 2]
100K [Human adenovirus 2]gi|56160503|ref|AP_000178.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024