NM_000335.5(SCN5A):c.4799T>A (p.Leu1600His) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003776601.1
Allele description [Variation Report for NM_000335.5(SCN5A):c.4799T>A (p.Leu1600His)]
NM_000335.5(SCN5A):c.4799T>A (p.Leu1600His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Vaginal neoplasm
Vaginal neoplasmMedGen
-
C0042258[conceptid] (1)
MedGen
-
PREDICTED: Homo sapiens trafficking from ER to golgi regulator (TFG), transcript...
PREDICTED: Homo sapiens trafficking from ER to golgi regulator (TFG), transcript variant X5, mRNAgi|2217341351|ref|XM_017005527.2|Nucleotide
-
eyes absent homolog 3 isoform c [Homo sapiens]
eyes absent homolog 3 isoform c [Homo sapiens]gi|543173155|ref|NP_001269490.1|Protein
-
Homo sapiens septin 9 (SEPTIN9), transcript variant 11, mRNA
Homo sapiens septin 9 (SEPTIN9), transcript variant 11, mRNAgi|1676317625|ref|NM_001293698.2|Nucleotide
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Last Updated: Sep 16, 2024