NM_000335.5(SCN5A):c.5082G>A (p.Gln1694=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003868811.2
Allele description [Variation Report for NM_000335.5(SCN5A):c.5082G>A (p.Gln1694=)]
NM_000335.5(SCN5A):c.5082G>A (p.Gln1694=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens immediate early response 5 (IER5), mRNA
Homo sapiens immediate early response 5 (IER5), mRNAgi|7706080|ref|NM_016545.1|Nucleotide
-
Homo sapiens inhibin, beta C (INHBC), mRNA
Homo sapiens inhibin, beta C (INHBC), mRNAgi|5031794|ref|NM_005538.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024