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NM_174934.3(SCN4B):c.239T>C (p.Ile80Thr) AND Long QT syndrome 10

Significance: Uncertain significance
ClinVar: RCV000227966

Variant: NM_174934.3(SCN4B):c.239T>C (p.Ile80Thr)

Type: Variant
Allele: NM_174934.3(SCN4B):c.239T>C (p.Ile80Thr) 241058
Gene:
Type: single nucleotide variant
Location: Chr11: 118014772 - assembly GRCh37
Chr11: 118144057 - assembly GRCh38
References: dbSNP: 546190140

Condition

Disease: Long QT syndrome 10