ClinVar Miner

List of variants in gene IFIH1 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_022168.4(IFIH1):c.2016del (p.Asp673fs) rs773033563 0.00028
NM_022168.4(IFIH1):c.2459G>A (p.Arg820His) rs74162087 0.00024
NM_022168.4(IFIH1):c.1312T>C (p.Ser438Pro) rs139714761 0.00010
NM_022168.4(IFIH1):c.1853G>A (p.Arg618Gln) rs200017837 0.00007
NM_022168.4(IFIH1):c.1243C>A (p.Gln415Lys) rs575678322 0.00006
NM_022168.4(IFIH1):c.2788A>C (p.Asn930His) rs374202040 0.00006
NM_022168.4(IFIH1):c.2456C>A (p.Ala819Asp) rs200810568 0.00004
NM_022168.4(IFIH1):c.2858A>G (p.Asp953Gly) rs148623633 0.00004
NM_022168.4(IFIH1):c.1166G>A (p.Gly389Glu) rs765985079 0.00003
NM_022168.4(IFIH1):c.104T>A (p.Leu35Gln) rs1235525082 0.00001
NM_022168.4(IFIH1):c.1294G>T (p.Val432Phe) rs1353805115 0.00001
NM_022168.4(IFIH1):c.137T>C (p.Ile46Thr) rs1276069749 0.00001
NM_022168.4(IFIH1):c.1710G>A (p.Met570Ile) rs776280813 0.00001
NM_022168.4(IFIH1):c.1765+1G>A rs1292220162 0.00001
NM_022168.4(IFIH1):c.1960T>G (p.Cys654Gly) rs987124852 0.00001
NM_022168.4(IFIH1):c.2398G>T (p.Glu800Ter) rs1444920926 0.00001
NM_022168.4(IFIH1):c.2724A>T (p.Lys908Asn) rs750467622 0.00001
NM_022168.4(IFIH1):c.77T>A (p.Ile26Asn) rs1442046271 0.00001
NM_022168.4(IFIH1):c.1070G>A (p.Gly357Glu)
NM_022168.4(IFIH1):c.1095+1G>A rs140125523
NM_022168.4(IFIH1):c.1095G>T (p.Lys365Asn)
NM_022168.4(IFIH1):c.113T>C (p.Leu38Pro) rs919140409
NM_022168.4(IFIH1):c.1229T>C (p.Ile410Thr) rs746025085
NM_022168.4(IFIH1):c.1283A>G (p.Glu428Gly) rs74162081
NM_022168.4(IFIH1):c.1358del (p.Val453fs)
NM_022168.4(IFIH1):c.1475G>A (p.Gly492Asp) rs1474848285
NM_022168.4(IFIH1):c.1550C>T (p.Thr517Ile) rs2105200508
NM_022168.4(IFIH1):c.165C>A (p.Asn55Lys)
NM_022168.4(IFIH1):c.1669A>T (p.Ile557Leu) rs2105198684
NM_022168.4(IFIH1):c.1721G>A (p.Gly574Glu)
NM_022168.4(IFIH1):c.1738C>T (p.Gln580Ter) rs774888783
NM_022168.4(IFIH1):c.1744G>A (p.Ala582Thr)
NM_022168.4(IFIH1):c.175G>A (p.Val59Ile)
NM_022168.4(IFIH1):c.1764dup (p.Ala589fs) rs553669430
NM_022168.4(IFIH1):c.1795del (p.Val599fs)
NM_022168.4(IFIH1):c.1847C>A (p.Thr616Lys)
NM_022168.4(IFIH1):c.1924G>A (p.Glu642Lys) rs748031255
NM_022168.4(IFIH1):c.2045-1G>T rs748813106
NM_022168.4(IFIH1):c.2067G>T (p.Arg689Ser) rs376420466
NM_022168.4(IFIH1):c.2134T>C (p.Tyr712His)
NM_022168.4(IFIH1):c.216C>G (p.His72Gln) rs774025268
NM_022168.4(IFIH1):c.2216_2222del (p.Thr739fs) rs745948096
NM_022168.4(IFIH1):c.2299A>G (p.Thr767Ala) rs766399254
NM_022168.4(IFIH1):c.229C>T (p.Arg77Trp) rs147278787
NM_022168.4(IFIH1):c.2303A>G (p.Gln768Arg) rs1085307464
NM_022168.4(IFIH1):c.2321_2323delinsGTT (p.Val774_Ile775delinsGlyPhe) rs2105193797
NM_022168.4(IFIH1):c.2372T>C (p.Val791Ala) rs2105193712
NM_022168.4(IFIH1):c.2455-6T>A rs2105192046
NM_022168.4(IFIH1):c.2483G>A (p.Ser828Asn)
NM_022168.4(IFIH1):c.2525A>G (p.Glu842Gly) rs775472922
NM_022168.4(IFIH1):c.2542G>A (p.Asp848Asn)
NM_022168.4(IFIH1):c.2554A>T (p.Lys852Ter)
NM_022168.4(IFIH1):c.2558T>C (p.Met853Thr) rs1691055209
NM_022168.4(IFIH1):c.2596C>T (p.Pro866Ser)
NM_022168.4(IFIH1):c.2667G>C (p.Lys889Asn)
NM_022168.4(IFIH1):c.2744G>A (p.Cys915Tyr)
NM_022168.4(IFIH1):c.2744G>C (p.Cys915Ser) rs2105187782
NM_022168.4(IFIH1):c.2872G>A (p.Gly958Ser) rs1466752669
NM_022168.4(IFIH1):c.2884T>C (p.Cys962Arg) rs1559808756
NM_022168.4(IFIH1):c.296T>A (p.Leu99His)
NM_022168.4(IFIH1):c.3004A>T (p.Lys1002Ter)
NM_022168.4(IFIH1):c.3025A>G (p.Thr1009Ala) rs1690942148
NM_022168.4(IFIH1):c.3068A>C (p.Asp1023Ala) rs2105186476
NM_022168.4(IFIH1):c.557G>T (p.Arg186Leu) rs189443152
NM_022168.4(IFIH1):c.627T>G (p.Ile209Met)
NM_022168.4(IFIH1):c.775G>C (p.Asp259His)
NM_022168.4(IFIH1):c.871T>A (p.Ser291Thr)

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