NM_001458.5(FLNC):c.22T>C (p.Ser8Pro) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 25, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001683701.1
Allele description [Variation Report for NM_001458.5(FLNC):c.22T>C (p.Ser8Pro)]
NM_001458.5(FLNC):c.22T>C (p.Ser8Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens cDNA clone IMAGE:40147494
Homo sapiens cDNA clone IMAGE:40147494gi|148753293|gb|BC142627.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024