ClinVar Miner

List of variants in gene combination FPGT-TNNI3K, LRRC53, TNNI3K reported as uncertain significance for atrial conduction disease

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Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_015978.3(TNNI3K):c.2157dup (p.Glu720fs) rs754423974 0.00031
NM_001382280.1(LRRC53):c.2543_2546dup (p.Glu849delinsAspTer) rs1416246083 0.00002
NM_015978.3(TNNI3K):c.2269C>T (p.Arg757Trp) rs201798397 0.00001
NM_001382280.1(LRRC53):c.2630C>T (p.Ala877Val)
NM_015978.3(TNNI3K):c.2177T>C (p.Ile726Thr)
NM_015978.3(TNNI3K):c.2205C>A (p.Asn735Lys) rs199608014
NM_015978.3(TNNI3K):c.2258G>C (p.Gly753Ala)
NM_015978.3(TNNI3K):c.2297G>C (p.Arg766Pro) rs201340993
NM_015978.3(TNNI3K):c.2309A>T (p.Glu770Val)

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