NM_016258.3(YTHDF2):c.634G>C (p.Gly212Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 13, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004120746.1
Allele description [Variation Report for NM_016258.3(YTHDF2):c.634G>C (p.Gly212Arg)]
NM_016258.3(YTHDF2):c.634G>C (p.Gly212Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024