ClinVar Miner

List of variants in gene IFT140 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP
NM_014714.4(IFT140):c.*2G>A rs144879630
NM_014714.4(IFT140):c.*403G>A
NM_014714.4(IFT140):c.*429C>T rs192256907
NM_014714.4(IFT140):c.*63A>G
NM_014714.4(IFT140):c.1541T>A (p.Leu514His) rs150903791
NM_014714.4(IFT140):c.1542C>A (p.Leu514=) rs141542834
NM_014714.4(IFT140):c.1831G>A (p.Val611Ile) rs35301526
NM_014714.4(IFT140):c.2542C>T (p.Arg848Cys) rs201384469
NM_014714.4(IFT140):c.2569G>A (p.Gly857Ser) rs200876696
NM_014714.4(IFT140):c.2988T>C (p.Asn996=) rs78178397
NM_014714.4(IFT140):c.3711C>T (p.Phe1237=) rs146172074
NM_014714.4(IFT140):c.3874-11C>T rs199887622
NM_014714.4(IFT140):c.3993G>C (p.Gln1331His) rs35823417
NM_014714.4(IFT140):c.4040+11G>A rs144624901

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