ClinVar Miner

List of variants in gene LPIN1 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_001349206.2(LPIN1):c.*1780A>G rs146105485 0.00275
NM_001349206.2(LPIN1):c.*1714C>T rs568958922 0.00260
NM_001349206.2(LPIN1):c.*1722del rs886054808 0.00186
NM_001349206.2(LPIN1):c.1922G>A (p.Arg641His) rs145021638 0.00101
NM_001349206.2(LPIN1):c.*777G>A rs150550941 0.00097
NM_001349206.2(LPIN1):c.1225C>G (p.Gln409Glu) rs146529487 0.00097
NM_001349206.2(LPIN1):c.*1263C>T rs183188041 0.00091
NM_001349206.2(LPIN1):c.*1430C>T rs570313304 0.00076
NM_001349206.2(LPIN1):c.*541C>T rs781193131 0.00071
NM_001349206.2(LPIN1):c.2661G>A (p.Pro887=) rs114931326 0.00071
NM_001349206.2(LPIN1):c.*2284A>G rs569760366 0.00066
NM_001349206.2(LPIN1):c.*1374G>C rs138644378 0.00063
NM_001349206.2(LPIN1):c.119A>G (p.Asn40Ser) rs149819112 0.00051
NM_001349206.2(LPIN1):c.2067G>T (p.Thr689=) rs369684215 0.00045
NM_001349206.2(LPIN1):c.429C>T (p.Ser143=) rs145629147 0.00032
NM_001349206.2(LPIN1):c.*538C>T rs531722548 0.00029
NM_001349206.2(LPIN1):c.1972G>A (p.Val658Ile) rs146048019 0.00025
NM_001349206.2(LPIN1):c.1886+7T>C rs200527588 0.00020
NM_001349206.2(LPIN1):c.138C>G (p.Ser46=) rs192688285 0.00019
NM_001349206.2(LPIN1):c.2674A>T (p.Ser892Cys) rs202129194 0.00017
NM_001349206.2(LPIN1):c.1293C>T (p.Asp431=) rs200898383 0.00011
NM_001349206.2(LPIN1):c.42C>T (p.Thr14=) rs146180669 0.00011
NM_001349206.2(LPIN1):c.*1708G>A rs142740836 0.00008
NM_001349206.2(LPIN1):c.2219G>A (p.Gly740Asp) rs369135035 0.00008
NM_001349206.2(LPIN1):c.2414A>G (p.Glu805Gly) rs771205777 0.00008
NM_001349206.2(LPIN1):c.1083G>A (p.Leu361=) rs548508177 0.00006
NM_001349206.2(LPIN1):c.1265-7G>A rs376096398 0.00006
NM_001349206.2(LPIN1):c.2342C>T (p.Thr781Met) rs149307854 0.00006
NM_001349206.2(LPIN1):c.2343G>A (p.Thr781=) rs139771618 0.00006
NM_001349206.2(LPIN1):c.72C>T (p.Pro24=) rs137942440 0.00006
NM_001349206.2(LPIN1):c.*2597C>T rs886054811 0.00003
NM_001349206.2(LPIN1):c.1663G>A (p.Ala555Thr) rs761610281 0.00003
NM_001349206.2(LPIN1):c.1924G>A (p.Ala642Thr) rs200394034 0.00003
NM_001349206.2(LPIN1):c.2393C>A (p.Ala798Asp) rs774737339 0.00003
NM_001349206.2(LPIN1):c.616C>G (p.Pro206Ala) rs370440936 0.00003
NM_001349206.2(LPIN1):c.*2213G>A rs775862577 0.00002
NM_001349206.2(LPIN1):c.*816A>G rs886054803 0.00002
NM_001349206.2(LPIN1):c.*99C>T rs886054800 0.00002
NM_001349206.2(LPIN1):c.24C>T (p.Ala8=) rs752905024 0.00002
NM_001349206.2(LPIN1):c.309G>T (p.Leu103=) rs140846512 0.00002
NM_001349206.2(LPIN1):c.*1100T>C rs1385055312 0.00001
NM_001349206.2(LPIN1):c.*1101C>T rs886054804 0.00001
NM_001349206.2(LPIN1):c.*1997C>T rs533093841 0.00001
NM_001349206.2(LPIN1):c.*2145A>G rs1302262311 0.00001
NM_001349206.2(LPIN1):c.*271G>A rs947280319 0.00001
NM_001349206.2(LPIN1):c.152G>A (p.Arg51His) rs766980528 0.00001
NM_001349206.2(LPIN1):c.1795A>G (p.Thr599Ala) rs758794799 0.00001
NM_001349206.2(LPIN1):c.2030A>T (p.Lys677Met) rs1678292863 0.00001
NM_001349206.2(LPIN1):c.2168A>G (p.Asp723Gly) rs767607996 0.00001
NM_001349206.2(LPIN1):c.2609C>G (p.Thr870Ser) rs758717162 0.00001
NM_001349206.2(LPIN1):c.597-4C>T rs777255851 0.00001
NM_001349206.2(LPIN1):c.695C>T (p.Ser232Leu) rs568970987 0.00001
NM_001349206.2(LPIN1):c.966T>C (p.Ser322=) rs777607912 0.00001
NM_001349206.2(LPIN1):c.*1066A>G rs1682302897
NM_001349206.2(LPIN1):c.*1339ATT[1] rs747138667
NM_001349206.2(LPIN1):c.*1343T>C rs886054806
NM_001349206.2(LPIN1):c.*1357G>C rs886054807
NM_001349206.2(LPIN1):c.*1487G>A rs764806697
NM_001349206.2(LPIN1):c.*1582T>G rs1034357247
NM_001349206.2(LPIN1):c.*1723A>C rs1682395137
NM_001349206.2(LPIN1):c.*1744A>G rs1573072063
NM_001349206.2(LPIN1):c.*1747del rs886054809
NM_001349206.2(LPIN1):c.*1772G>C rs1024124067
NM_001349206.2(LPIN1):c.*2005del rs886054810
NM_001349206.2(LPIN1):c.*2029G>A rs866544426
NM_001349206.2(LPIN1):c.*2052C>T rs563773982
NM_001349206.2(LPIN1):c.*404G>T rs886054801
NM_001349206.2(LPIN1):c.*676C>G rs886054802
NM_001349206.2(LPIN1):c.*704A>G rs1682257150
NM_001349206.2(LPIN1):c.*927A>G rs1682284905
NM_001349206.2(LPIN1):c.110G>A (p.Arg37His) rs774490262
NM_001349206.2(LPIN1):c.124A>G (p.Asn42Asp) rs886054796
NM_001349206.2(LPIN1):c.1790A>G (p.Asn597Ser) rs886054799
NM_001349206.2(LPIN1):c.1852G>A (p.Gly618Arg) rs146100011
NM_001349206.2(LPIN1):c.1886+5G>A rs201689636
NM_001349206.2(LPIN1):c.2043C>T (p.Asn681=) rs372109726
NM_001349206.2(LPIN1):c.2150G>T (p.Gly717Val) rs1678319978
NM_001349206.2(LPIN1):c.2403-8T>G rs371725918
NM_001349206.2(LPIN1):c.438G>A (p.Pro146=) rs762701125
NM_001349206.2(LPIN1):c.524C>T (p.Thr175Ile) rs1165035642
NM_001349206.2(LPIN1):c.688C>T (p.Pro230Ser) rs886054797
NM_001349206.2(LPIN1):c.722+4A>G rs886054798

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