ClinVar Miner

List of variants in gene LIFR reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 146
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001127671.2(LIFR):c.364A>G (p.Thr122Ala) rs145163157 0.00131
NM_001127671.2(LIFR):c.670A>G (p.Ile224Val) rs151282774 0.00108
NM_001127671.2(LIFR):c.2302A>G (p.Arg768Gly) rs139848756 0.00107
NM_001127671.2(LIFR):c.247A>G (p.Ile83Val) rs61751710 0.00068
NM_001127671.2(LIFR):c.2410A>G (p.Lys804Glu) rs148664975 0.00056
NM_001127671.2(LIFR):c.2948C>G (p.Pro983Arg) rs146856673 0.00044
NM_001127671.2(LIFR):c.1267A>G (p.Ile423Val) rs144606459 0.00042
NM_001127671.2(LIFR):c.263G>A (p.Arg88His) rs61751711 0.00042
NM_001127671.2(LIFR):c.46G>A (p.Asp16Asn) rs61751713 0.00029
NM_001127671.2(LIFR):c.3221A>G (p.Asp1074Gly) rs147058538 0.00022
NM_001127671.2(LIFR):c.452C>G (p.Ser151Cys) rs61751712 0.00015
NM_001127671.2(LIFR):c.410A>G (p.Asp137Gly) rs773284026 0.00011
NM_001127671.2(LIFR):c.2280G>A (p.Leu760=) rs370455274 0.00010
NM_001127671.2(LIFR):c.2591+6A>T rs372291945 0.00009
NM_001127671.2(LIFR):c.2937G>A (p.Ser979=) rs201711670 0.00008
NM_001127671.2(LIFR):c.1171G>A (p.Glu391Lys) rs373421600 0.00004
NM_001127671.2(LIFR):c.2462C>G (p.Pro821Arg) rs139248720 0.00004
NM_001127671.2(LIFR):c.728A>G (p.Asn243Ser) rs771895582 0.00004
NM_001127671.2(LIFR):c.1290A>G (p.Lys430=) rs1418919413 0.00003
NM_001127671.2(LIFR):c.1806C>A (p.Asp602Glu) rs145286888 0.00003
NM_001127671.2(LIFR):c.2338C>T (p.Arg780Cys) rs553912841 0.00003
NM_001127671.2(LIFR):c.2670+6C>G rs898718526 0.00003
NM_001127671.2(LIFR):c.3086G>A (p.Arg1029Lys) rs1012911330 0.00003
NM_001127671.2(LIFR):c.1004C>T (p.Thr335Ile) rs769942217 0.00002
NM_001127671.2(LIFR):c.1424C>T (p.Ser475Leu) rs763060076 0.00002
NM_001127671.2(LIFR):c.1485T>C (p.Ala495=) rs759537735 0.00002
NM_001127671.2(LIFR):c.2887G>A (p.Ala963Thr) rs770022153 0.00002
NM_001127671.2(LIFR):c.3089C>T (p.Pro1030Leu) rs1439167190 0.00002
NM_001127671.2(LIFR):c.1319A>G (p.Lys440Arg) rs1250493020 0.00001
NM_001127671.2(LIFR):c.1357T>C (p.Trp453Arg) rs201516825 0.00001
NM_001127671.2(LIFR):c.1439G>A (p.Arg480Gln) rs781727104 0.00001
NM_001127671.2(LIFR):c.1460T>C (p.Val487Ala) rs1429532863 0.00001
NM_001127671.2(LIFR):c.1493A>G (p.Lys498Arg) rs771697399 0.00001
NM_001127671.2(LIFR):c.1517C>T (p.Thr506Ile) rs1264340150 0.00001
NM_001127671.2(LIFR):c.1721C>T (p.Ser574Leu) rs142407999 0.00001
NM_001127671.2(LIFR):c.1776C>G (p.His592Gln) rs762360996 0.00001
NM_001127671.2(LIFR):c.2282T>C (p.Phe761Ser) rs1287071072 0.00001
NM_001127671.2(LIFR):c.2548G>T (p.Val850Phe) rs1466625336 0.00001
NM_001127671.2(LIFR):c.3197G>A (p.Arg1066Gln) rs368698516 0.00001
NM_001127671.2(LIFR):c.3245G>A (p.Gly1082Glu) rs775530423 0.00001
NM_001127671.2(LIFR):c.3275A>G (p.Gln1092Arg) rs1460896687 0.00001
NM_001127671.2(LIFR):c.406C>G (p.Pro136Ala) rs761024368 0.00001
NM_001127671.2(LIFR):c.425T>C (p.Leu142Ser) rs779962357 0.00001
NM_001127671.2(LIFR):c.962A>G (p.Asn321Ser) rs202224745 0.00001
NM_001127671.2(LIFR):c.1021T>A (p.Cys341Ser)
NM_001127671.2(LIFR):c.1079C>T (p.Ala360Val)
NM_001127671.2(LIFR):c.1162C>T (p.Pro388Ser)
NM_001127671.2(LIFR):c.1180C>A (p.Gln394Lys)
NM_001127671.2(LIFR):c.1182ATT[2] (p.Leu396del) rs754991843
NM_001127671.2(LIFR):c.1190T>G (p.Phe397Cys)
NM_001127671.2(LIFR):c.1199T>C (p.Leu400Pro) rs2112471546
NM_001127671.2(LIFR):c.1226C>T (p.Thr409Ile)
NM_001127671.2(LIFR):c.1229T>G (p.Leu410Trp)
NM_001127671.2(LIFR):c.1280T>A (p.Ile427Lys) rs1241596011
NM_001127671.2(LIFR):c.1298C>T (p.Pro433Leu)
NM_001127671.2(LIFR):c.1301A>G (p.His434Arg)
NM_001127671.2(LIFR):c.1306C>T (p.Pro436Ser)
NM_001127671.2(LIFR):c.1388A>G (p.Asn463Ser)
NM_001127671.2(LIFR):c.1438-3T>G
NM_001127671.2(LIFR):c.1491C>G (p.Asp497Glu)
NM_001127671.2(LIFR):c.14A>G (p.Tyr5Cys)
NM_001127671.2(LIFR):c.1516A>C (p.Thr506Pro) rs1057524477
NM_001127671.2(LIFR):c.1578ACA[1] (p.Gln527del) rs1373344377
NM_001127671.2(LIFR):c.1599C>A (p.Ala533=)
NM_001127671.2(LIFR):c.1622C>T (p.Thr541Ile)
NM_001127671.2(LIFR):c.1705C>G (p.Leu569Val) rs544925449
NM_001127671.2(LIFR):c.1708T>A (p.Ser570Thr) rs2112430998
NM_001127671.2(LIFR):c.1714A>G (p.Asn572Asp)
NM_001127671.2(LIFR):c.1780G>A (p.Ala594Thr) rs752038840
NM_001127671.2(LIFR):c.1819G>C (p.Val607Leu)
NM_001127671.2(LIFR):c.1838T>C (p.Val613Ala)
NM_001127671.2(LIFR):c.183A>C (p.Gln61His) rs1243202901
NM_001127671.2(LIFR):c.1843T>C (p.Ser615Pro)
NM_001127671.2(LIFR):c.184G>A (p.Val62Met)
NM_001127671.2(LIFR):c.1886A>G (p.Asp629Gly) rs372374955
NM_001127671.2(LIFR):c.1898T>C (p.Ile633Thr)
NM_001127671.2(LIFR):c.1919G>A (p.Gly640Glu) rs2112417801
NM_001127671.2(LIFR):c.1970A>G (p.Tyr657Cys)
NM_001127671.2(LIFR):c.1975A>T (p.Ile659Phe)
NM_001127671.2(LIFR):c.1997G>A (p.Arg666Gln) rs748647105
NM_001127671.2(LIFR):c.2009G>A (p.Cys670Tyr)
NM_001127671.2(LIFR):c.2041A>G (p.Ser681Gly) rs973820530
NM_001127671.2(LIFR):c.2053G>A (p.Val685Ile)
NM_001127671.2(LIFR):c.205G>A (p.Ala69Thr) rs1299060827
NM_001127671.2(LIFR):c.2080G>A (p.Gly694Ser)
NM_001127671.2(LIFR):c.2137C>T (p.Arg713Cys)
NM_001127671.2(LIFR):c.2167+5G>A rs1377181323
NM_001127671.2(LIFR):c.2243C>T (p.Pro748Leu)
NM_001127671.2(LIFR):c.2284T>C (p.Tyr762His)
NM_001127671.2(LIFR):c.2307C>A (p.Asp769Glu) rs1288146568
NM_001127671.2(LIFR):c.2336-3T>C rs754392969
NM_001127671.2(LIFR):c.2349A>G (p.Ile783Met)
NM_001127671.2(LIFR):c.2377C>G (p.Gln793Glu) rs2112377617
NM_001127671.2(LIFR):c.2423A>G (p.His808Arg) rs1580002991
NM_001127671.2(LIFR):c.2497+14T>A
NM_001127671.2(LIFR):c.2558T>G (p.Val853Gly)
NM_001127671.2(LIFR):c.2611C>T (p.Pro871Ser)
NM_001127671.2(LIFR):c.2679T>G (p.Ser893Arg)
NM_001127671.2(LIFR):c.2683C>T (p.Leu895Phe) rs749556499
NM_001127671.2(LIFR):c.2720A>G (p.Asn907Ser)
NM_001127671.2(LIFR):c.2741G>A (p.Arg914Gln)
NM_001127671.2(LIFR):c.2744C>T (p.Ser915Leu)
NM_001127671.2(LIFR):c.2759T>C (p.Ile920Thr)
NM_001127671.2(LIFR):c.2794C>T (p.Arg932Cys)
NM_001127671.2(LIFR):c.2875C>A (p.Pro959Thr)
NM_001127671.2(LIFR):c.287C>A (p.Thr96Asn)
NM_001127671.2(LIFR):c.2962GAA[2] (p.Glu990del) rs761535056
NM_001127671.2(LIFR):c.2968G>C (p.Glu990Gln)
NM_001127671.2(LIFR):c.2986G>A (p.Val996Ile)
NM_001127671.2(LIFR):c.2995G>T (p.Ala999Ser)
NM_001127671.2(LIFR):c.3002A>G (p.Tyr1001Cys)
NM_001127671.2(LIFR):c.3015G>A (p.Met1005Ile) rs898747115
NM_001127671.2(LIFR):c.3077C>T (p.Ala1026Val)
NM_001127671.2(LIFR):c.3131C>T (p.Ser1044Phe) rs755926450
NM_001127671.2(LIFR):c.314A>G (p.His105Arg)
NM_001127671.2(LIFR):c.3166T>C (p.Ser1056Pro)
NM_001127671.2(LIFR):c.317G>A (p.Gly106Asp)
NM_001127671.2(LIFR):c.3217A>G (p.Lys1073Glu)
NM_001127671.2(LIFR):c.3231_3232del (p.Ser1077_Pro1078insTer) rs776513402
NM_001127671.2(LIFR):c.3254G>A (p.Trp1085Ter)
NM_001127671.2(LIFR):c.3267C>G (p.Asn1089Lys)
NM_001127671.2(LIFR):c.3288C>A (p.Asn1096Lys) rs3729751
NM_001127671.2(LIFR):c.3289G>A (p.Asp1097Asn)
NM_001127671.2(LIFR):c.328A>G (p.Ile110Val)
NM_001127671.2(LIFR):c.3290A>T (p.Asp1097Val)
NM_001127671.2(LIFR):c.334A>G (p.Ile112Val)
NM_001127671.2(LIFR):c.397+3A>C
NM_001127671.2(LIFR):c.413C>G (p.Thr138Ser) rs1580108976
NM_001127671.2(LIFR):c.416C>T (p.Pro139Leu)
NM_001127671.2(LIFR):c.457T>G (p.Leu153Val)
NM_001127671.2(LIFR):c.499C>T (p.Arg167Cys)
NM_001127671.2(LIFR):c.4A>G (p.Met2Val)
NM_001127671.2(LIFR):c.500G>A (p.Arg167His)
NM_001127671.2(LIFR):c.569A>C (p.His190Pro) rs1298466429
NM_001127671.2(LIFR):c.607_621del (p.Trp203_Ser207del) rs2112498961
NM_001127671.2(LIFR):c.626T>C (p.Met209Thr)
NM_001127671.2(LIFR):c.640G>A (p.Ala214Thr)
NM_001127671.2(LIFR):c.659T>C (p.Ile220Thr)
NM_001127671.2(LIFR):c.692G>T (p.Gly231Val)
NM_001127671.2(LIFR):c.697G>A (p.Glu233Lys)
NM_001127671.2(LIFR):c.788T>A (p.Val263Glu)
NM_001127671.2(LIFR):c.853A>G (p.Thr285Ala)
NM_001127671.2(LIFR):c.860G>T (p.Cys287Phe) rs1745744862
NM_001127671.2(LIFR):c.904C>T (p.Arg302Cys)
NM_001127671.2(LIFR):c.907A>G (p.Asn303Asp)
NM_001127671.2(LIFR):c.955G>A (p.Glu319Lys)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.