NM_000492.4(CFTR):c.721G>A (p.Gly241Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003317065.1
Allele description [Variation Report for NM_000492.4(CFTR):c.721G>A (p.Gly241Arg)]
NM_000492.4(CFTR):c.721G>A (p.Gly241Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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See more...Assertion and evidence details
Last Updated: Jul 29, 2023