ClinVar Miner

List of variants in gene IFIH1 reported as likely benign for not provided

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Gene type:
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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_022168.4(IFIH1):c.2808-75G>T rs3761652 0.03297
NM_022168.4(IFIH1):c.2454+275C>A rs41463049 0.03291
NM_022168.4(IFIH1):c.1524+90G>A rs16846555 0.03287
NM_022168.4(IFIH1):c.623-251A>G rs12478636 0.02967
NM_022168.4(IFIH1):c.770-104A>C rs12474958 0.02949
NM_022168.4(IFIH1):c.770-101T>G rs12478730 0.02946
NM_022168.4(IFIH1):c.2808-231A>G rs17764770 0.02603
NM_022168.4(IFIH1):c.2767A>G (p.Ile923Val) rs35667974 0.01195
NM_022168.4(IFIH1):c.622+121A>G rs17715295 0.00833
NM_022168.4(IFIH1):c.875-34C>T rs35502110 0.00696
NM_022168.4(IFIH1):c.2305-135G>A rs2287290 0.00660
NM_022168.4(IFIH1):c.2807+1G>A rs35732034 0.00502
NM_022168.4(IFIH1):c.1524+185A>G rs114572831 0.00474
NM_022168.4(IFIH1):c.258C>G (p.Thr86=) rs143870870 0.00424
NM_022168.4(IFIH1):c.1766-119C>T rs146400109 0.00407
NM_022168.4(IFIH1):c.1879G>T (p.Glu627Ter) rs35744605 0.00367
NM_022168.4(IFIH1):c.2105C>T (p.Thr702Ile) rs72650663 0.00253
NM_022168.4(IFIH1):c.2946C>T (p.Leu982=) rs74162089 0.00240
NM_022168.4(IFIH1):c.1481G>T (p.Gly494Val) rs147000317 0.00228
NM_022168.4(IFIH1):c.2785G>A (p.Val929Ile) rs140562355 0.00214
NM_022168.4(IFIH1):c.2863C>G (p.Gln955Glu) rs144455277 0.00113
NM_022168.4(IFIH1):c.1046A>G (p.Lys349Arg) rs72650664 0.00111
NM_022168.4(IFIH1):c.478A>G (p.Asn160Asp) rs74162075 0.00079
NM_022168.4(IFIH1):c.1066C>A (p.Pro356Thr) rs150317197 0.00078
NM_022168.4(IFIH1):c.2524G>A (p.Glu842Lys) rs79324540 0.00076
NM_022168.4(IFIH1):c.1583T>G (p.Leu528Arg) rs142348767 0.00049
NM_022168.4(IFIH1):c.1121G>A (p.Arg374His) rs145520044 0.00041
NM_022168.4(IFIH1):c.420G>A (p.Glu140=) rs74162073 0.00026
NM_022168.4(IFIH1):c.2597C>T (p.Pro866Leu) rs200833729 0.00025
NM_022168.4(IFIH1):c.453+5G>C rs548027236 0.00021
NM_022168.4(IFIH1):c.2682G>A (p.Lys894=) rs374488772 0.00019
NM_022168.4(IFIH1):c.1312T>C (p.Ser438Pro) rs139714761 0.00010
NM_022168.4(IFIH1):c.906G>A (p.Pro302=) rs775441863 0.00010
NM_022168.4(IFIH1):c.2295C>A (p.Pro765=) rs769746385 0.00006
NM_022168.4(IFIH1):c.261C>T (p.Gly87=) rs775555538 0.00005
NM_022168.4(IFIH1):c.1642-8A>G rs772580594 0.00004
NM_022168.4(IFIH1):c.1710G>A (p.Met570Ile) rs776280813 0.00001
NM_022168.4(IFIH1):c.3036T>A (p.Asn1012Lys) rs528639734 0.00001
NM_022168.4(IFIH1):c.1035T>C (p.Asp345=) rs1576229553
NM_022168.4(IFIH1):c.1095+98_1095+102del rs141134657
NM_022168.4(IFIH1):c.1306+189A>G rs115921156
NM_022168.4(IFIH1):c.1560T>C (p.Thr520=)
NM_022168.4(IFIH1):c.1641+8C>T rs780592381
NM_022168.4(IFIH1):c.1996C>T (p.Pro666Ser) rs376074455
NM_022168.4(IFIH1):c.2020_2023del (p.Arg674fs) rs569337014
NM_022168.4(IFIH1):c.2103G>A (p.Leu701=) rs1576224311
NM_022168.4(IFIH1):c.229C>T (p.Arg77Trp) rs147278787
NM_022168.4(IFIH1):c.403T>C (p.Leu135=) rs1576243156
NM_022168.4(IFIH1):c.653C>T (p.Pro218Leu) rs539777490
NM_022168.4(IFIH1):c.663A>G (p.Glu221=)
NM_022168.4(IFIH1):c.744T>G (p.Ser248=)

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