ClinVar Miner

List of variants in gene INF2 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_022489.4(INF2):c.105C>T (p.Pro35=) rs4983530 0.98049
NM_022489.4(INF2):c.2640T>C (p.Asp880=) rs10133301 0.88426
NM_022489.4(INF2):c.3066T>C (p.Asp1022=) rs4983535 0.79980
NM_022489.4(INF2):c.2310+8del rs3840006 0.58720
NM_022489.4(INF2):c.2775+15C>T rs73347508 0.06749
NM_022489.4(INF2):c.3286C>T (p.Pro1096Ser) rs34251364 0.05864
NM_022489.4(INF2):c.843+16C>T rs118017785 0.05808
NM_022489.4(INF2):c.2322C>T (p.Thr774=) rs59751492 0.02373
NM_022489.4(INF2):c.391+18A>T rs115458897 0.02077
NM_022489.4(INF2):c.2571C>T (p.Ser857=) rs62640005 0.01396
NM_022489.4(INF2):c.42G>A (p.Leu14=) rs62638758 0.01192
NM_022489.4(INF2):c.3153C>T (p.Asp1051=) rs117457867 0.01185
NM_022489.4(INF2):c.391+17G>A rs4074531 0.01087
NM_022489.4(INF2):c.1281_1286del (p.Pro428_Leu429del) rs751555478 0.00781
NM_022489.4(INF2):c.2630G>A (p.Arg877Gln) rs142678449 0.00781
NM_022489.4(INF2):c.1547C>T (p.Pro516Leu) rs111589086 0.00779
NM_022489.4(INF2):c.879G>A (p.Ser293=) rs184709736 0.00543
NM_022489.4(INF2):c.3108T>C (p.Leu1036=) rs186075307 0.00532
NM_022489.4(INF2):c.1078G>A (p.Val360Ile) rs114820975 0.00483
NM_022489.4(INF2):c.3069C>T (p.Pro1023=) rs75382114 0.00477
NM_022489.4(INF2):c.2458C>T (p.Arg820Trp) rs79327775 0.00247
NM_022489.4(INF2):c.3404C>T (p.Thr1135Met) rs3803311 0.00242
NM_022489.4(INF2):c.2138+9G>A rs201065953 0.00213
NM_022489.4(INF2):c.558C>T (p.Ser186=) rs150714865 0.00158
NM_022489.4(INF2):c.264C>T (p.Gly88=) rs201587219 0.00150
NM_022489.4(INF2):c.1281A>C (p.Pro427=) rs754332692 0.00140
NM_022489.4(INF2):c.3612G>A (p.Ser1204=) rs150811244 0.00134
NM_022489.4(INF2):c.3134G>A (p.Arg1045Gln) rs200369827 0.00126
NM_022489.4(INF2):c.2848C>T (p.Arg950Trp) rs199873407 0.00098
NM_022489.4(INF2):c.1144A>G (p.Ser382Gly) rs201077878 0.00048
NM_022489.4(INF2):c.3638G>A (p.Arg1213Gln) rs199801767 0.00047
NM_022489.4(INF2):c.1773C>T (p.Asp591=) rs201853087 0.00038
NM_022489.4(INF2):c.3747G>A (p.Gln1249=) rs149939482 0.00036
NM_022489.4(INF2):c.37G>A (p.Ala13Thr) rs201383094 0.00034
NM_022489.4(INF2):c.2509C>T (p.Arg837Cys) rs201534539 0.00033
NM_022489.4(INF2):c.639G>A (p.Ala213=) rs149858291 0.00031
NM_022489.4(INF2):c.1632T>C (p.His544=) rs374940901 0.00030
NM_022489.4(INF2):c.1929C>T (p.Ile643=) rs756712490 0.00026
NM_022489.4(INF2):c.2885A>C (p.Lys962Thr) rs376067427 0.00023
NM_022489.4(INF2):c.1736-18C>T rs199612826 0.00022
NM_022489.4(INF2):c.1264C>T (p.Pro422Ser) rs767748953 0.00012
NM_022489.4(INF2):c.744C>T (p.Phe248=) rs372799744 0.00012
NM_022489.4(INF2):c.1770C>T (p.Pro590=) rs549506051 0.00011
NM_022489.4(INF2):c.1458C>T (p.Phe486=) rs1420347614 0.00010
NM_022489.4(INF2):c.2622G>A (p.Ser874=) rs374311535 0.00009
NM_022489.4(INF2):c.1448C>T (p.Ser483Phe) rs753188664 0.00006
NM_022489.4(INF2):c.2755C>G (p.Leu919Val) rs377145979 0.00006
NM_022489.4(INF2):c.3591G>A (p.Ala1197=) rs765090867 0.00006
NM_022489.4(INF2):c.1485G>A (p.Pro495=) rs780642540 0.00005
NM_022489.4(INF2):c.1587C>T (p.Pro529=) rs755649066 0.00005
NM_022489.4(INF2):c.2879-9G>A rs373139405 0.00005
NM_022489.4(INF2):c.2043G>A (p.Glu681=) rs776591878 0.00004
NM_022489.4(INF2):c.3057T>C (p.Pro1019=) rs770151373 0.00004
NM_022489.4(INF2):c.519C>T (p.Ser173=) rs780247558 0.00004
NM_022489.4(INF2):c.3435C>T (p.Ala1145=) rs780026536 0.00003
NM_022489.4(INF2):c.288G>C (p.Leu96=) rs557082203 0.00002
NM_022489.4(INF2):c.1115C>T (p.Ser372Phe) rs770882784 0.00001
NM_022489.4(INF2):c.1605G>A (p.Glu535=) rs374316478 0.00001
NM_022489.4(INF2):c.3509G>A (p.Gly1170Glu) rs776092624 0.00001
NM_022489.4(INF2):c.489C>T (p.Asp163=) rs769080446 0.00001
NM_022489.4(INF2):c.624C>T (p.Pro208=) rs750610272 0.00001
NM_022489.4(INF2):c.*2-14TC[3]
NM_022489.4(INF2):c.1018C>A (p.Arg340=)
NM_022489.4(INF2):c.1077C>T (p.Ser359=)
NM_022489.4(INF2):c.1188C>G (p.Pro396=) rs747696039
NM_022489.4(INF2):c.1188C>T (p.Pro396=) rs747696039
NM_022489.4(INF2):c.1217_1228del (p.Leu406_Ser409del)
NM_022489.4(INF2):c.1348G>A (p.Gly450Arg) rs572969666
NM_022489.4(INF2):c.149A>C (p.Tyr50Ser) rs730880113
NM_022489.4(INF2):c.1506A>C (p.Pro502=)
NM_022489.4(INF2):c.1512A>C (p.Pro504=)
NM_022489.4(INF2):c.1524T>G (p.Pro508=)
NM_022489.4(INF2):c.1736-10C>T
NM_022489.4(INF2):c.2127G>A (p.Leu709=)
NM_022489.4(INF2):c.2313C>T (p.Gly771=)
NM_022489.4(INF2):c.255G>A (p.Ser85=) rs369037445
NM_022489.4(INF2):c.2617A>G (p.Ile873Val)
NM_022489.4(INF2):c.2709G>C (p.Gln903His) rs762803590
NM_022489.4(INF2):c.303C>T (p.Cys101=)
NM_022489.4(INF2):c.3049A>C (p.Ser1017Arg)
NM_022489.4(INF2):c.3166G>A (p.Gly1056Ser)
NM_022489.4(INF2):c.3207A>C (p.Pro1069=) rs1128840
NM_022489.4(INF2):c.3207A>G (p.Pro1069=) rs1128840
NM_022489.4(INF2):c.391+6C>T rs75115369
NM_022489.4(INF2):c.392-13_392-9dup rs775575983
NM_022489.4(INF2):c.556T>C (p.Ser186Pro) rs267606877
NM_022489.4(INF2):c.698T>C (p.Leu233Pro)
NM_022489.4(INF2):c.814C>T (p.Gln272Ter)

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