NM_002180.3(IGHMBP2):c.1482C>T (p.Ala494=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 7, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000612360.1
Allele description [Variation Report for NM_002180.3(IGHMBP2):c.1482C>T (p.Ala494=)]
NM_002180.3(IGHMBP2):c.1482C>T (p.Ala494=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
DNA (cytosine-5)-methyltransferase 3B isoform X5 [Homo sapiens]
DNA (cytosine-5)-methyltransferase 3B isoform X5 [Homo sapiens]gi|2462579699|ref|XP_054179095.1|Protein
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Last Updated: Sep 29, 2024