NM_001080510.5(METTL23):c.406A>G (p.Ser136Gly) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 21, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000203093.1
Allele description [Variation Report for NM_001080510.5(METTL23):c.406A>G (p.Ser136Gly)]
NM_001080510.5(METTL23):c.406A>G (p.Ser136Gly)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens SprT-like N-terminal domain (SPRTN), transcript variant 2, mRNA
Homo sapiens SprT-like N-terminal domain (SPRTN), transcript variant 2, mRNAgi|1675132866|ref|NM_001010984.4|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 7, 2024