ClinVar Miner

List of variants in gene LOC130065679, SNTA1 studied for long QT syndrome

Included ClinVar conditions (78):
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Gene type:
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Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_003098.3(SNTA1):c.287G>C (p.Gly96Ala) rs766925398 0.00014
NM_003098.3(SNTA1):c.255G>C (p.Arg85=) rs1335742203 0.00003
NM_003098.3(SNTA1):c.272G>T (p.Arg91Leu)
NM_003098.3(SNTA1):c.273dup (p.Lys92fs)
NM_003098.3(SNTA1):c.275A>G (p.Lys92Arg)
NM_003098.3(SNTA1):c.277G>A (p.Ala93Thr) rs886056627
NM_003098.3(SNTA1):c.279C>A (p.Ala93=) rs1178951223
NM_003098.3(SNTA1):c.280G>C (p.Asp94His) rs786205844
NM_003098.3(SNTA1):c.292C>T (p.Leu98=) rs2146814454
NM_003098.3(SNTA1):c.304dup (p.Ile102fs)

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