NM_000335.5(SCN5A):c.592T>C (p.Phe198Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002302601.1
Allele description [Variation Report for NM_000335.5(SCN5A):c.592T>C (p.Phe198Leu)]
NM_000335.5(SCN5A):c.592T>C (p.Phe198Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Human aldehyde dehydrogenase mRNA, complete cds
Human aldehyde dehydrogenase mRNA, complete cdsgi|178374|gb|M77477.1|HUMALDDENucleotide
-
"Premature loss of teeth"[Clinical Features] OR 66678[uid] (24)
MedGen
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Nov 13, 2022