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NM_174934.3(SCN4B):c.617C>T (p.Ser206Leu) AND Long QT syndrome 10

Significance: Uncertain significance
ClinVar: RCV000234662

Variant: NM_174934.3(SCN4B):c.617C>T (p.Ser206Leu)

Type: Variant
Allele: NM_174934.3(SCN4B):c.617C>T (p.Ser206Leu) 189321
Gene:
Type: single nucleotide variant
Location: Chr11: 118007812 - assembly GRCh37
Chr11: 117513022 - assembly NCBI36
Chr11: 118137097 - assembly GRCh38
References: dbSNP: 140348243

Condition

Disease: Long QT syndrome 10