ClinVar Miner

List of variants in gene KLF11 reported as uncertain significance for digestive system disorder

Included ClinVar conditions (605):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_003597.5(KLF11):c.*738A>G rs146942100 0.00117
NM_003597.5(KLF11):c.*1608T>G rs142746538 0.00096
NM_003597.5(KLF11):c.*2265T>A rs757068768 0.00054
NM_003597.5(KLF11):c.953T>G (p.Leu318Arg) rs144431930 0.00048
NM_003597.5(KLF11):c.*756C>T rs886054727 0.00041
NM_003597.5(KLF11):c.*2273C>T rs534714754 0.00029
NM_003597.5(KLF11):c.*216_*217insTT rs1553314463 0.00026
NM_003597.5(KLF11):c.1102C>T (p.Pro368Ser) rs144897109 0.00023
NM_003597.5(KLF11):c.*1155G>A rs886054729 0.00021
NM_003597.5(KLF11):c.*654C>T rs144723641 0.00021
NM_003597.5(KLF11):c.*1658G>A rs367805998 0.00019
NM_003597.5(KLF11):c.*674G>C rs574996537 0.00019
NM_003597.5(KLF11):c.*956C>T rs149067484 0.00016
NM_003597.5(KLF11):c.992G>T (p.Gly331Val) rs151317435 0.00016
NM_003597.5(KLF11):c.437C>T (p.Ala146Val) rs148968483 0.00015
NM_003597.5(KLF11):c.*166C>T rs531131204 0.00011
NM_003597.5(KLF11):c.*1386A>G rs886054732 0.00010
NM_003597.5(KLF11):c.1077G>A (p.Met359Ile) rs146486664 0.00009
NM_003597.5(KLF11):c.961G>C (p.Ala321Pro) rs776725808 0.00009
NM_003597.5(KLF11):c.608G>A (p.Gly203Glu) rs145588324 0.00008
NM_003597.5(KLF11):c.*1301C>G rs886054731 0.00007
NM_003597.5(KLF11):c.*217G>T rs201145049 0.00007
NM_003597.5(KLF11):c.266C>T (p.Ala89Val) rs766187124 0.00007
NM_003597.5(KLF11):c.1137C>G (p.Ser379Arg) rs199624763 0.00006
NM_003597.5(KLF11):c.673A>C (p.Ser225Arg) rs200061013 0.00006
NM_003597.5(KLF11):c.1169G>A (p.Arg390Gln) rs563767876 0.00005
NM_003597.5(KLF11):c.1304T>A (p.Phe435Tyr) rs752588055 0.00005
NM_003597.5(KLF11):c.*1990T>C rs911685125 0.00004
NM_003597.5(KLF11):c.1259-2_1259-1del rs770555623 0.00004
NM_003597.5(KLF11):c.689C>T (p.Ser230Phe) rs370039403 0.00004
NM_003597.5(KLF11):c.1396A>T (p.Ser466Cys) rs757875185 0.00003
NM_003597.5(KLF11):c.23G>A (p.Gly8Asp) rs1553312826 0.00003
NM_003597.5(KLF11):c.305C>G (p.Ser102Trp) rs576350323 0.00003
NM_003597.5(KLF11):c.358A>G (p.Arg120Gly) rs201792575 0.00003
NM_003597.5(KLF11):c.431T>C (p.Val144Ala) rs753049849 0.00003
NM_003597.5(KLF11):c.*1320G>A rs555032852 0.00002
NM_003597.5(KLF11):c.*2081C>T rs886054736 0.00002
NM_003597.5(KLF11):c.*954C>G rs886054728 0.00002
NM_003597.5(KLF11):c.811A>C (p.Lys271Gln) rs368207952 0.00002
NM_003597.5(KLF11):c.994C>T (p.Pro332Ser) rs375265808 0.00002
NM_003597.5(KLF11):c.*131G>A rs545836068 0.00001
NM_003597.5(KLF11):c.*1463A>G rs1572448681 0.00001
NM_003597.5(KLF11):c.*1636C>T rs886054735 0.00001
NM_003597.5(KLF11):c.*1725G>C rs374263399 0.00001
NM_003597.5(KLF11):c.*2103G>A rs1056465665 0.00001
NM_003597.5(KLF11):c.1046C>T (p.Pro349Leu) rs886054723 0.00001
NM_003597.5(KLF11):c.1049C>T (p.Pro350Leu) rs775364750 0.00001
NM_003597.5(KLF11):c.1486G>A (p.Ala496Thr) rs868399686 0.00001
NM_003597.5(KLF11):c.18C>T (p.Phe6=) rs886054722 0.00001
NM_003597.5(KLF11):c.259A>G (p.Met87Val) rs757905542 0.00001
NM_003597.5(KLF11):c.25C>T (p.Pro9Ser) rs1377863567 0.00001
NM_003597.5(KLF11):c.501C>T (p.Pro167=) rs377399356 0.00001
NM_003597.5(KLF11):c.928T>C (p.Ser310Pro) rs759266535 0.00001
NM_003597.5(KLF11):c.*1296T>C rs886054730
NM_003597.5(KLF11):c.*1495G>A rs886054733
NM_003597.5(KLF11):c.*1612C>G rs886054734
NM_003597.5(KLF11):c.*1894A>G rs557209557
NM_003597.5(KLF11):c.*319C>T rs777727299
NM_003597.5(KLF11):c.*457A>T rs920552860
NM_003597.5(KLF11):c.*96dup rs886054725
NM_003597.5(KLF11):c.1037G>T (p.Gly346Val) rs964899969
NM_003597.5(KLF11):c.1057C>A (p.Pro353Thr) rs886054724
NM_003597.5(KLF11):c.1396A>G (p.Ser466Gly) rs757875185
NM_003597.5(KLF11):c.308C>T (p.Thr103Ile)
NM_003597.5(KLF11):c.351A>G (p.Pro117=) rs781433096
NM_003597.5(KLF11):c.57C>A (p.Asp19Glu)
NM_003597.5(KLF11):c.608_609delinsAG (p.Gly203Glu) rs1057524882
NM_003597.5(KLF11):c.644A>G (p.Gln215Arg) rs1347317649
NM_003597.5(KLF11):c.926T>C (p.Leu309Ser) rs1661291203

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