NM_000335.5(SCN5A):c.611+11C>G AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003773847.2
Allele description [Variation Report for NM_000335.5(SCN5A):c.611+11C>G]
NM_000335.5(SCN5A):c.611+11C>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens cDNA FLJ13656 fis, clone PLACE1011520
Homo sapiens cDNA FLJ13656 fis, clone PLACE1011520gi|10435733|dbj|AK023718.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024