ClinVar Miner

List of variants in gene IFIH1 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_022168.4(IFIH1):c.2528A>G (p.His843Arg) rs3747517 0.68382
NM_022168.4(IFIH1):c.2836G>A (p.Ala946Thr) rs1990760 0.44895
NM_022168.4(IFIH1):c.2767A>G (p.Ile923Val) rs35667974 0.01195
NM_022168.4(IFIH1):c.1641+1G>C rs35337543 0.00728
NM_022168.4(IFIH1):c.2807+1G>A rs35732034 0.00502
NM_022168.4(IFIH1):c.258C>G (p.Thr86=) rs143870870 0.00424
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.2362G>A (p.Ala788Thr) rs148369169 0.00207
NM_022168.4(IFIH1):c.1723A>G (p.Thr575Ala) rs138057665 0.00162
NM_022168.4(IFIH1):c.436A>G (p.Ile146Val) rs146721166 0.00129
NM_022168.4(IFIH1):c.1097T>A (p.Val366Glu) rs140977021 0.00121
NM_022168.4(IFIH1):c.1046A>G (p.Lys349Arg) rs72650664 0.00111
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.1965T>A (p.Asp655Glu) rs144274375 0.00054
NM_022168.4(IFIH1):c.1121G>A (p.Arg374His) rs145520044 0.00041
NM_022168.4(IFIH1):c.2392A>G (p.Ile798Val) rs758387388 0.00031
NM_022168.4(IFIH1):c.2597C>T (p.Pro866Leu) rs200833729 0.00025
NM_022168.4(IFIH1):c.2459G>A (p.Arg820His) rs74162087 0.00024
NM_022168.4(IFIH1):c.1407T>C (p.Asn469=) rs138740030 0.00014
NM_022168.4(IFIH1):c.2232T>A (p.Phe744Leu) rs201142986 0.00007
NM_022168.4(IFIH1):c.2919G>C (p.Val973=) rs376116707 0.00007
NM_022168.4(IFIH1):c.2115A>C (p.Arg705Ser) rs185928139 0.00006
NM_022168.4(IFIH1):c.2295C>A (p.Pro765=) rs769746385 0.00006
NM_022168.4(IFIH1):c.1524+9T>C rs74162083 0.00004
NM_022168.4(IFIH1):c.2414T>G (p.Ile805Ser) rs753623939 0.00004
NM_022168.4(IFIH1):c.1166G>A (p.Gly389Glu) rs765985079 0.00003
NM_022168.4(IFIH1):c.1658A>T (p.Lys553Ile) rs749596514 0.00002
NM_022168.4(IFIH1):c.2019T>C (p.Asp673=) rs779835794 0.00002
NM_022168.4(IFIH1):c.1142T>C (p.Leu381Ser) rs764148204 0.00001
NM_022168.4(IFIH1):c.2321T>A (p.Val774Asp) rs1246892209 0.00001
NM_022168.4(IFIH1):c.2724A>T (p.Lys908Asn) rs750467622 0.00001
NM_022168.4(IFIH1):c.919C>T (p.Gln307Ter) rs762821474 0.00001
NM_022168.4(IFIH1):c.1387A>T (p.Met463Leu) rs1247355630
NM_022168.4(IFIH1):c.1499C>G (p.Ala500Gly)
NM_022168.4(IFIH1):c.1764dup (p.Ala589fs) rs553669430
NM_022168.4(IFIH1):c.1766-11dup rs548261817
NM_022168.4(IFIH1):c.1766C>A (p.Ala589Asp) rs145792185
NM_022168.4(IFIH1):c.1810T>C (p.Leu604=)
NM_022168.4(IFIH1):c.1815G>C (p.Arg605Ser)
NM_022168.4(IFIH1):c.1827G>T (p.Glu609Asp)
NM_022168.4(IFIH1):c.1828G>A (p.Ala610Thr)
NM_022168.4(IFIH1):c.199G>C (p.Glu67Gln) rs2105238398
NM_022168.4(IFIH1):c.2020_2023del (p.Arg674fs) rs569337014
NM_022168.4(IFIH1):c.229C>T (p.Arg77Trp) rs147278787
NM_022168.4(IFIH1):c.2454+4C>T rs886038669
NM_022168.4(IFIH1):c.259G>T (p.Gly87Cys)
NM_022168.4(IFIH1):c.389T>C (p.Leu130Pro) rs1683537130
NM_022168.4(IFIH1):c.557G>C (p.Arg186Pro) rs189443152
NM_022168.4(IFIH1):c.742T>C (p.Ser248Pro) rs1392840230

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