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NM_174934.3(SCN4B):c.174C>T (p.Cys58=) AND Long QT syndrome 10

Significance: Benign
ClinVar: RCV000476805

Variant: NM_174934.3(SCN4B):c.174C>T (p.Cys58=)

Type: Variant
Allele: NM_174934.3(SCN4B):c.174C>T (p.Cys58=) 142740
Gene:
Type: single nucleotide variant
Location: Chr11: 118015832 - assembly GRCh37
Chr11: 118145117 - assembly GRCh38
References: dbSNP: 45539032

Condition

Disease: Long QT syndrome 10