ClinVar Miner

List of variants in gene IFT140 reported as benign for not provided

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_014714.4(IFT140):c.3454-48A>G rs932391 0.45637
NM_014714.4(IFT140):c.2200-42T>C rs2235641 0.35692
NM_014714.4(IFT140):c.*59T>C rs1053730 0.34440
NM_014714.4(IFT140):c.4041-44T>C rs2076434 0.24775
NM_014714.4(IFT140):c.2067+205T>G rs28714146 0.24021
NM_014714.4(IFT140):c.3453+34C>T rs34819117 0.15720
NM_014714.4(IFT140):c.3271-53G>A rs78028801 0.10498
NM_014714.4(IFT140):c.4183-172C>T rs67356424 0.09472
NM_014714.4(IFT140):c.4040+171C>T rs67733554 0.08517
NM_014714.4(IFT140):c.2577+193G>C rs113971932 0.08333
NM_014714.4(IFT140):c.1771-236A>T rs116908844 0.05066
NM_014714.4(IFT140):c.1682G>A (p.Ser561Asn) rs8050974 0.02675
NM_014714.4(IFT140):c.1525-185C>T rs78154916 0.02506
NM_014714.4(IFT140):c.1918G>A (p.Asp640Asn) rs61742753 0.02347
NM_014714.4(IFT140):c.4380C>T (p.Asp1460=) rs61749517 0.02245
NM_014714.4(IFT140):c.2008C>T (p.Pro670Ser) rs34900355 0.02198
NM_014714.4(IFT140):c.2454C>T (p.Asp818=) rs34668993 0.01885
NM_014714.4(IFT140):c.3743T>C (p.Ile1248Thr) rs79494390 0.01709
NM_014714.4(IFT140):c.2578-157G>A rs8053047 0.01666
NM_014714.4(IFT140):c.3142-73C>G rs2076437 0.01571
NM_014714.4(IFT140):c.2068-29del rs113397794
NM_014714.4(IFT140):c.2068-39dup rs113397794
NM_014714.4(IFT140):c.2577+184C>T rs115039155
NM_014714.4(IFT140):c.4183-188G>T rs67551650

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