ClinVar Miner

List of variants in gene IFIH1 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 59
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HGVS dbSNP gnomAD frequency
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.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.2362G>A (p.Ala788Thr) rs148369169 0.00207
NM_022168.4(IFIH1):c.2863C>G (p.Gln955Glu) rs144455277 0.00113
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.2016del (p.Asp673fs) rs773033563 0.00028
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.445A>G (p.Arg149Gly) rs74162074 0.00024
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.1558A>G (p.Thr520Ala) rs145641024 0.00016
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.1853G>A (p.Arg618Gln) rs200017837 0.00007
NM_022168.4(IFIH1):c.2642T>C (p.Ile881Thr) rs745487097 0.00007
NM_022168.4(IFIH1):c.2295C>A (p.Pro765=) rs769746385 0.00006
NM_022168.4(IFIH1):c.2299del (p.Thr767fs) rs759430873 0.00006
NM_022168.4(IFIH1):c.2893G>A (p.Gly965Ser) rs202009944 0.00006
NM_022168.4(IFIH1):c.1222G>A (p.Asp408Asn) rs148540097 0.00005
NM_022168.4(IFIH1):c.261C>T (p.Gly87=) rs775555538 0.00005
NM_022168.4(IFIH1):c.1873C>A (p.His625Asn) rs749942019 0.00004
NM_022168.4(IFIH1):c.2548C>T (p.Arg850Ter) rs750804689 0.00004
NM_022168.4(IFIH1):c.2857G>A (p.Asp953Asn) rs751417093 0.00004
NM_022168.4(IFIH1):c.2045-1G>A rs748813106 0.00003
NM_022168.4(IFIH1):c.2305-2A>G rs199696786 0.00003
NM_022168.4(IFIH1):c.2465G>A (p.Arg822Gln) rs376048533 0.00003
NM_022168.4(IFIH1):c.*7del rs760571400 0.00002
NM_022168.4(IFIH1):c.1710G>A (p.Met570Ile) rs776280813 0.00001
NM_022168.4(IFIH1):c.505A>T (p.Lys169Ter) rs201495678 0.00001
NM_022168.4(IFIH1):c.524A>T (p.Glu175Val) rs759418219 0.00001
NM_022168.4(IFIH1):c.919C>T (p.Gln307Ter) rs762821474 0.00001
NM_022168.4(IFIH1):c.1126G>A (p.Glu376Lys)
NM_022168.4(IFIH1):c.113T>C (p.Leu38Pro) rs919140409
NM_022168.4(IFIH1):c.1165G>A (p.Gly389Arg) rs1576227162
NM_022168.4(IFIH1):c.1560T>C (p.Thr520=)
NM_022168.4(IFIH1):c.1568A>G (p.Glu523Gly)
NM_022168.4(IFIH1):c.1916C>A (p.Ala639Glu)
NM_022168.4(IFIH1):c.1930G>A (p.Asp644Asn) rs1553459020
NM_022168.4(IFIH1):c.1996C>T (p.Pro666Ser) rs376074455
NM_022168.4(IFIH1):c.229C>T (p.Arg77Trp) rs147278787
NM_022168.4(IFIH1):c.2335C>T (p.Arg779Cys) rs587777448
NM_022168.4(IFIH1):c.2336G>A (p.Arg779His) rs587777446
NM_022168.4(IFIH1):c.2405A>C (p.Asn802Thr)
NM_022168.4(IFIH1):c.557G>T (p.Arg186Leu) rs189443152
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=)
NM_022168.4(IFIH1):c.789_804del (p.Glu264fs)
NM_022168.4(IFIH1):c.969G>T (p.Lys323Asn) rs1682931607
NM_022168.4(IFIH1):c.971A>G (p.Asn324Ser) rs2105209017

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