NM_014727.3(KMT2B):c.5932G>A (p.Glu1978Lys) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 4, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003852398.2
Allele description [Variation Report for NM_014727.3(KMT2B):c.5932G>A (p.Glu1978Lys)]
NM_014727.3(KMT2B):c.5932G>A (p.Glu1978Lys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens paired like homeobox 2B (PHOX2B), mRNA
Homo sapiens paired like homeobox 2B (PHOX2B), mRNAgi|172072680|ref|NM_003924.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024