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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


291 records found for search term Klf11
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
11550056CV250077single nucleotide variantNM_003597.5(KLF11):c.-9G>Anot specified [RCV000251238]likely benign21004370810043708Humanname
150535962CV1309073single nucleotide variantNM_003597.5(KLF11):c.*43C>Tnot provided [RCV001759280]likely benign21005255010052550Humanname
11651418CV281466duplicationNM_003597.5(KLF11):c.*96dupMaturity onset diabetes mellitus in young [RCV000298714]uncertain significance21005259510052596Human1name
11652981CV283451single nucleotide variantNM_003597.5(KLF11):c.-31G>AMaturity-onset diabetes of the young type 7 [RCV000308079]uncertain significance21004368610043686Human1name
28874300CV880756single nucleotide variantNM_003597.5(KLF11):c.-83G>AMaturity-onset diabetes of the young type 7 [RCV001133321]uncertain significance21004363410043634Human1name
28874305CV880757single nucleotide variantNM_003597.5(KLF11):c.-76G>AMaturity-onset diabetes of the young type 7 [RCV001133322]uncertain significance21004364110043641Human1name
150543479CV1308990single nucleotide variantNM_003597.5(KLF11):c.-157C>Tnot provided [RCV001769903]likely benign21004356010043560Humanname
150535923CV1309056single nucleotide variantNM_003597.5(KLF11):c.*218T>Gnot provided [RCV001759263]likely benign21005272510052725Humanname
152146749CV1655946single nucleotide variantNM_003597.5(KLF11):c.43-9C>Tnot provided [RCV002220168]likely benign21004614110046141Humanname
11591577CV281470single nucleotide variantNM_003597.5(KLF11):c.*166C>TMaturity-onset diabetes of the young type 7 [RCV000330206]uncertain significance21005267310052673Human1name
11596848CV281474single nucleotide variantNM_003597.5(KLF11):c.*192T>CMaturity-onset diabetes of the young type 7 [RCV000387231]benign|uncertain significance21005269910052699Human1name
11586242CV281477single nucleotide variantNM_003597.5(KLF11):c.*241A>GMaturity-onset diabetes of the young type 7 [RCV000286414]|not provided [RCV001764300]benign|likely benign21005274810052748Human1name
11592682CV281478single nucleotide variantNM_003597.5(KLF11):c.*435A>TMaturity-onset diabetes of the young type 7 [RCV000341368]|not provided [RCV004708345]benign|likely benign21005294210052942Human1name
11589137CV281485single nucleotide variantNM_003597.5(KLF11):c.*980T>CMaturity-onset diabetes of the young type 7 [RCV000308312]benign|likely benign21005348710053487Human1name
11594790CV281494single nucleotide variantNM_003597.5(KLF11):c.*982G>AMaturity-onset diabetes of the young type 7 [RCV000363011]likely benign|uncertain significance21005348910053489Human1name
11595407CV282117single nucleotide variantNM_003597.5(KLF11):c.*107G>AMaturity-onset diabetes of the young type 7 [RCV000369758]benign|likely benign21005261410052614Human1name
11596272CV282118single nucleotide variantNM_003597.5(KLF11):c.*235T>CMaturity-onset diabetes of the young type 7 [RCV000380470]|not provided [RCV001753792]benign|likely benign21005274210052742Human1name
11587643CV282120single nucleotide variantNM_003597.5(KLF11):c.*612C>TMaturity-onset diabetes of the young type 7 [RCV000296835]benign|likely benign21005311910053119Human1name
11592363CV282121single nucleotide variantNM_003597.5(KLF11):c.*674G>CMaturity-onset diabetes of the young type 7 [RCV000337831]uncertain significance21005318110053181Human1name
11589621CV282132single nucleotide variantNM_003597.5(KLF11):c.*882G>AMaturity-onset diabetes of the young type 7 [RCV000311923]benign|likely benign21005338910053389Human1name
11663956CV283429single nucleotide variantNM_003597.5(KLF11):c.-146C>TMaturity-onset diabetes of the young type 7 [RCV000400988]uncertain significance21004357110043571Human1name
11653221CV283436single nucleotide variantNM_003597.5(KLF11):c.-104C>TMaturity-onset diabetes of the young type 7 [RCV000309523]|not provided [RCV004694461]uncertain significance21004361310043613Human1name
11584173CV283469single nucleotide variantNM_003597.5(KLF11):c.*194G>AMaturity-onset diabetes of the young type 7 [RCV000271753]|not provided [RCV001764299]benign|likely benign21005270110052701Human1name
11592750CV283479single nucleotide variantNM_003597.5(KLF11):c.*217G>TMaturity-onset diabetes of the young type 7 [RCV000342177]uncertain significance21005272410052724Human1name
11598138CV283482single nucleotide variantNM_003597.5(KLF11):c.*544C>AMaturity-onset diabetes of the young type 7 [RCV000401814]|not provided [RCV004708346]benign|likely benign21005305110053051Human1name
11663029CV283483single nucleotide variantNM_003597.5(KLF11):c.*756C>TMaturity-onset diabetes of the young type 7 [RCV000391512]uncertain significance21005326310053263Human1name
11660919CV283486single nucleotide variantNM_003597.5(KLF11):c.*954C>GMaturity-onset diabetes of the young type 7 [RCV000371385]uncertain significance21005346110053461Human1name
11584828CV283487single nucleotide variantNM_003597.5(KLF11):c.*956C>TMaturity onset diabetes mellitus in young [RCV000276813]uncertain significance21005346310053463Human1name
11584951CV283605single nucleotide variantNM_003597.5(KLF11):c.*131G>AMaturity-onset diabetes of the young type 7 [RCV000277448]uncertain significance21005263810052638Human1name
11635730CV283606duplicationNM_003597.5(KLF11):c.*227dupMaturity onset diabetes mellitus in young [RCV000381505]|not provided [RCV001707655]benign|likely benign21005272410052725Human1name
405202066CV3067009single nucleotide variantNM_003597.5(KLF11):c.43-6C>Gnot provided [RCV003730872]likely benign21004614410046144Humanname
597956515CV3792437single nucleotide variantNM_003597.5(KLF11):c.43-8G>Anot provided [RCV005137324]likely benign21004614210046142Humanname
28874294CV880754single nucleotide variantNM_003597.5(KLF11):c.-159G>AMaturity-onset diabetes of the young type 7 [RCV001133319]uncertain significance21004355810043558Human1name
28874297CV880755single nucleotide variantNM_003597.5(KLF11):c.-108G>AMaturity-onset diabetes of the young type 7 [RCV001133320]uncertain significance21004360910043609Human1name
28868366CV880777single nucleotide variantNM_003597.5(KLF11):c.*122C>TMaturity-onset diabetes of the young type 7 [RCV001129894]likely benign21005262910052629Human1name
28869355CV880778single nucleotide variantNM_003597.5(KLF11):c.*262C>TMaturity-onset diabetes of the young type 7 [RCV001130599]benign21005276910052769Human1name
28869358CV880779single nucleotide variantNM_003597.5(KLF11):c.*319C>TMaturity-onset diabetes of the young type 7 [RCV001130600]uncertain significance21005282610052826Human1name
28874734CV880780single nucleotide variantNM_003597.5(KLF11):c.*457A>TMaturity-onset diabetes of the young type 7 [RCV001133546]uncertain significance21005296410052964Human1name
28874737CV880781single nucleotide variantNM_003597.5(KLF11):c.*654C>TMaturity-onset diabetes of the young type 7 [RCV001133547]uncertain significance21005316110053161Human1name
28874739CV880782single nucleotide variantNM_003597.5(KLF11):c.*738A>GMaturity-onset diabetes of the young type 7 [RCV001133548]uncertain significance21005324510053245Human1name
28878080CV880783single nucleotide variantNM_003597.5(KLF11):c.*981G>AMaturity-onset diabetes of the young type 7 [RCV001135037]benign21005348810053488Human1name
150464506CV1217540single nucleotide variantNM_003597.5(KLF11):c.42+85A>Gnot provided [RCV001613961]benign21004384310043843Humanname
152112362CV1539267deletionNM_003597.5(KLF11):c.313-3delnot provided [RCV002080424]benign21004763810047638Humanname
152042253CV1624203single nucleotide variantNM_003597.5(KLF11):c.42+19G>Anot provided [RCV002126241]likely benign21004377710043777Humanname
152118056CV1644022single nucleotide variantNM_003597.5(KLF11):c.42+18C>GMaturity-onset diabetes of the young type 7 [RCV002500248]|not provided [RCV002135353]likely benign21004377610043776Human1name
11585306CV281495single nucleotide variantNM_003597.5(KLF11):c.*1558T>CMaturity-onset diabetes of the young type 7 [RCV000280015]|not provided [RCV004708347]benign21005406510054065Human1name
11661387CV281505single nucleotide variantNM_003597.5(KLF11):c.*1612C>GMaturity-onset diabetes of the young type 7 [RCV000375726]uncertain significance21005411910054119Human1name
11588880CV281506single nucleotide variantNM_003597.5(KLF11):c.*2144C>TMaturity-onset diabetes of the young type 7 [RCV000306354]benign|likely benign21005465110054651Human1name
11646920CV282133single nucleotide variantNM_003597.5(KLF11):c.*1155G>AMaturity-onset diabetes of the young type 7 [RCV000273251]uncertain significance21005366210053662Human1name
11661594CV282134single nucleotide variantNM_003597.5(KLF11):c.*1301C>GMaturity-onset diabetes of the young type 7 [RCV000377927]uncertain significance21005380810053808Human1name
11593539CV282135single nucleotide variantNM_003597.5(KLF11):c.*1781T>CMaturity-onset diabetes of the young type 7 [RCV000349725]|not provided [RCV004708348]benign|likely benign21005428810054288Human1name
11587560CV282136single nucleotide variantNM_003597.5(KLF11):c.*1894A>GMaturity-onset diabetes of the young type 7 [RCV000295844]uncertain significance21005440110054401Human1name
11593650CV282139single nucleotide variantNM_003597.5(KLF11):c.*2026G>CMaturity-onset diabetes of the young type 7 [RCV000350730]benign|likely benign21005453310054533Human1name
11664066CV282140single nucleotide variantNM_003597.5(KLF11):c.*2081C>TMaturity-onset diabetes of the young type 7 [RCV000402110]uncertain significance21005458810054588Human1name
11595020CV282141single nucleotide variantNM_003597.5(KLF11):c.*2265T>AMaturity-onset diabetes of the young type 7 [RCV000365585]uncertain significance21005477210054772Human1name
11655811CV283492single nucleotide variantNM_003597.5(KLF11):c.*1296T>CMaturity-onset diabetes of the young type 7 [RCV000328308]uncertain significance21005380310053803Human1name
11590156CV283493single nucleotide variantNM_003597.5(KLF11):c.*1608T>GMaturity-onset diabetes of the young type 7 [RCV000316357]uncertain significance21005411510054115Human1name
11648340CV283494single nucleotide variantNM_003597.5(KLF11):c.*1636C>TMaturity-onset diabetes of the young type 7 [RCV000281209]uncertain significance21005414310054143Human1name
11597107CV283502single nucleotide variantNM_003597.5(KLF11):c.*1853T>CMaturity-onset diabetes of the young type 7 [RCV000390306]|not provided [RCV004709860]benign21005436010054360Human1name
11645304CV283607single nucleotide variantNM_003597.5(KLF11):c.*1386A>GMaturity-onset diabetes of the young type 7 [RCV000264641]uncertain significance21005389310053893Human1name
11590974CV283608single nucleotide variantNM_003597.5(KLF11):c.*1423T>CMaturity-onset diabetes of the young type 7 [RCV000324342]benign|likely benign21005393010053930Human1name
11661704CV283609single nucleotide variantNM_003597.5(KLF11):c.*1495G>AMaturity-onset diabetes of the young type 7 [RCV000378994]uncertain significance21005400210054002Human1name
11597304CV283622single nucleotide variantNM_003597.5(KLF11):c.*2273C>TMaturity-onset diabetes of the young type 7 [RCV000392577]uncertain significance21005478010054780Human1name
11588444CV283625single nucleotide variantNM_003597.5(KLF11):c.*2274G>AMaturity-onset diabetes of the young type 7 [RCV000303198]likely benign|uncertain significance21005478110054781Human1name
405183744CV3147969single nucleotide variantNM_003597.5(KLF11):c.42+10G>Anot provided [RCV003842679]uncertain significance21004376810043768Humanname
597860501CV3770104single nucleotide variantNM_003597.5(KLF11):c.312+9A>Tnot provided [RCV005105956]likely benign21004642810046428Humanname
28868509CV880784single nucleotide variantNM_003597.5(KLF11):c.*1320G>AMaturity-onset diabetes of the young type 7 [RCV001130008]uncertain significance21005382710053827Human1name
28868511CV880785single nucleotide variantNM_003597.5(KLF11):c.*1463A>GMaturity-onset diabetes of the young type 7 [RCV001130009]uncertain significance21005397010053970Human1name
28869575CV880786single nucleotide variantNM_003597.5(KLF11):c.*1658G>AMaturity-onset diabetes of the young type 7 [RCV001130722]uncertain significance21005416510054165Human1name
28869578CV880787single nucleotide variantNM_003597.5(KLF11):c.*1725G>CMaturity-onset diabetes of the young type 7 [RCV001130723]uncertain significance21005423210054232Human1name
28874969CV880788single nucleotide variantNM_003597.5(KLF11):c.*1990T>CMaturity-onset diabetes of the young type 7 [RCV001133681]uncertain significance21005449710054497Human1name
28874973CV880789single nucleotide variantNM_003597.5(KLF11):c.*2103G>AMaturity-onset diabetes of the young type 7 [RCV001133682]uncertain significance21005461010054610Human1name
150455781CV1236790single nucleotide variantNM_003597.5(KLF11):c.42+264G>Tnot provided [RCV001648526]benign21004402210044022Humanname
150545158CV1307646single nucleotide variantNM_003597.5(KLF11):c.42+310C>Tnot provided [RCV001774924]likely benign21004406810044068Humanname
11660415CV281440microsatelliteNM_003597.5(KLF11):c.-95GCC[5]Maturity onset diabetes mellitus in young [RCV000366591]|not provided [RCV001712118]benign21004362210043624Humanname
11664573CV281448microsatelliteNM_003597.5(KLF11):c.-95GCC[7]not provided [RCV002221527]benign|likely benign|uncertain significance21004362110043622Humanname
405269835CV3197926single nucleotide variantNM_003597.5(KLF11):c.312+10G>TKLF11-related disorder [RCV003899739]likely benign21004642910046429Humanname , trait , alternate_id
597928803CV3851840single nucleotide variantNM_003597.5(KLF11):c.313-17G>Tnot provided [RCV005206308]likely benign21004763310047633Humanname
150450610CV1272405single nucleotide variantNM_003597.5(KLF11):c.313-244G>Cnot provided [RCV001691886]benign21004740610047406Humanname
150541618CV1306474single nucleotide variantNM_003597.5(KLF11):c.313-266T>Cnot provided [RCV001768096]likely benign21004738410047384Humanname
150539252CV1308547single nucleotide variantNM_003597.5(KLF11):c.313-207C>Gnot provided [RCV001766051]likely benign21004744310047443Humanname
150432904CV1231582deletionNM_003597.5(KLF11):c.1258+335delnot provided [RCV001643244]benign21004890910048909Humanname
150453868CV1232180duplicationNM_003597.5(KLF11):c.1258+335dupnot provided [RCV001648193]benign21004890810048909Humanname
150431153CV1235352single nucleotide variantNM_003597.5(KLF11):c.1259-312C>Tnot provided [RCV001641722]benign21005191510051915Humanname
150541696CV1306507duplicationNM_003597.5(KLF11):c.*225_*227dupnot provided [RCV001768129]likely benign21005272410052725Humanname
11586637CV281475duplicationNM_003597.5(KLF11):c.*226_*227dupMaturity onset diabetes mellitus in young [RCV000289498]|not provided [RCV001597094]benign21005272410052725Human1name
156177782CV1953252duplicationNM_003597.5(KLF11):c.42+16_42+29dupnot provided [RCV002574018]uncertain significance21004377110043772Humanname
11655919CV283470insertionNM_003597.5(KLF11):c.*216_*217insTTMaturity onset diabetes mellitus in young [RCV000329270]uncertain significance21005272310052724Human1name
151355098CV1328165single nucleotide variantNM_003597.5(KLF11):c.24C>G (p.Gly8=)not specified [RCV001819641]likely benign21004374010043740Humanname
152033724CV1542764single nucleotide variantNM_003597.5(KLF11):c.12G>A (p.Pro4=)not provided [RCV002106625]likely benign21004372810043728Humanname
11659683CV282103single nucleotide variantNM_003597.5(KLF11):c.18C>T (p.Phe6=)Maturity-onset diabetes of the young type 7 [RCV000360429]uncertain significance21004373410043734Human1name
151353799CV1327351single nucleotide variantNM_003597.5(KLF11):c.33C>T (p.Asp11=)not provided [RCV002541984]|not specified [RCV001817295]likely benign21004374910043749Humanname
156112287CV2069191single nucleotide variantNM_003597.5(KLF11):c.36G>A (p.Ala12=)not provided [RCV002870944]likely benign21004375210043752Humanname
405088971CV3138158single nucleotide variantNM_003597.5(KLF11):c.42A>G (p.Ala14=)not provided [RCV003834676]uncertain significance21004375810043758Humanname
14693174CV620731deletionNM_003597.5(KLF11):c.1259-2_1259-1delnot provided [RCV002536734]uncertain significance21005222510052226Humanname
150532489CV1306766single nucleotide variantNM_003597.5(KLF11):c.225C>T (p.Val75=)Maturity-onset diabetes of the young type 7 [RCV002503245]|not provided [RCV001757764]benign|likely benign21004633210046332Human1name
152111723CV1532098single nucleotide variantNM_003597.5(KLF11):c.196C>T (p.Leu66=)not provided [RCV002116630]benign21004630310046303Humanname
156283977CV2050087single nucleotide variantNM_003597.5(KLF11):c.189A>G (p.Lys63=)not provided [RCV002807085]likely benign21004629610046296Humanname
401760881CV2726571single nucleotide variantNM_003597.5(KLF11):c.20C>T (p.Ala7Val)not specified [RCV004329065]uncertain significance21004373610043736Humanname
405207276CV2873937single nucleotide variantNM_003597.5(KLF11):c.177A>G (p.Gln59=)not provided [RCV003552002]likely benign21004628410046284Humanname
405295485CV3216032single nucleotide variantNM_003597.5(KLF11):c.252T>A (p.Thr84=)KLF11-related disorder [RCV003937403]likely benign21004635910046359Humanname , trait , alternate_id
597954204CV3757163single nucleotide variantNM_003597.5(KLF11):c.183C>A (p.Ser61=)not provided [RCV005080024]likely benign21004629010046290Humanname
597913721CV3771023single nucleotide variantNM_003597.5(KLF11):c.14A>G (p.Asp5Gly)not provided [RCV005114142]uncertain significance21004373010043730Humanname
597944626CV3793769single nucleotide variantNM_003597.5(KLF11):c.141T>C (p.Ala47=)not provided [RCV005134409]likely benign21004624810046248Humanname
13215299CV427869single nucleotide variantNM_003597.5(KLF11):c.22G>C (p.Gly8Arg)not specified [RCV000502339]uncertain significance21004373810043738Humanname
13612225CV513905single nucleotide variantNM_003597.5(KLF11):c.23G>A (p.Gly8Asp)Maturity onset diabetes mellitus in young [RCV000626848]uncertain significance21004373910043739Human2name
15169545CV696930variationNM_003597.5(KLF11):c.1185= (p.Val395=)not provided [RCV000949478]benign21004852210048522Humanname
28877457CV880758single nucleotide variantNM_003597.5(KLF11):c.25C>T (p.Pro9Ser)Maturity-onset diabetes of the young type 7 [RCV001134794]uncertain significance21004374110043741Human1name
151354087CV1327639single nucleotide variantNM_003597.5(KLF11):c.333C>T (p.Ser111=)not specified [RCV001817583]likely benign21004767010047670Humanname
156159358CV1906784single nucleotide variantNM_003597.5(KLF11):c.49A>G (p.Ile17Val)not provided [RCV003082831]|not specified [RCV004073240]likely benign|uncertain significance21004615610046156Humanname
156025465CV2037229single nucleotide variantNM_003597.5(KLF11):c.714T>C (p.Ser238=)not provided [RCV002795791]likely benign21004805110048051Humanname
329401432CV2460828single nucleotide variantNM_003597.5(KLF11):c.74T>C (p.Leu25Pro)not specified [RCV004271141]uncertain significance21004618110046181Humanname
401860921CV2750321single nucleotide variantNM_003597.5(KLF11):c.57C>A (p.Asp19Glu)Maturity-onset diabetes of the young type 7 [RCV003333865]uncertain significance21004616410046164Human1name
11577818CV282104single nucleotide variantNM_003597.5(KLF11):c.86G>A (p.Arg29Gln)Maturity-onset diabetes of the young type 7 [RCV000268105]|Monogenic diabetes [RCV000445417]|not provided [RCV001514109]benign|likely benign21004619310046193Human2name
11579077CV282111single nucleotide variantNM_003597.5(KLF11):c.429C>T (p.Ala143=)Maturity-onset diabetes of the young type 7 [RCV000294839]|not provided [RCV000946592]|not specified [RCV001553588]benign|likely benign21004776610047766Human1name
11580440CV282112single nucleotide variantNM_003597.5(KLF11):c.486A>G (p.Pro162=)Maturity-onset diabetes of the young type 7 [RCV000333478]|not provided [RCV002285316]|not specified [RCV003151030]benign|likely benign|uncertain significance21004782310047823Human1name
405069555CV2876350single nucleotide variantNM_003597.5(KLF11):c.915C>T (p.Pro305=)not provided [RCV003548445]likely benign21004825210048252Humanname
402466673CV2914887single nucleotide variantNM_003597.5(KLF11):c.312G>C (p.Leu104=)not provided [RCV003569505]uncertain significance21004641910046419Humanname
405219574CV3063370single nucleotide variantNM_003597.5(KLF11):c.876G>A (p.Val292=)KLF11-related disorder [RCV003901335]|not provided [RCV003733105]likely benign21004821310048213Human1name , trait , alternate_id
405220173CV3063410single nucleotide variantNM_003597.5(KLF11):c.408G>A (p.Thr136=)not provided [RCV003733130]likely benign21004774510047745Humanname
405209803CV3065582single nucleotide variantNM_003597.5(KLF11):c.459G>A (p.Ala153=)not provided [RCV003731732]likely benign21004779610047796Humanname
405191677CV3069997single nucleotide variantNM_003597.5(KLF11):c.834C>A (p.Val278=)not provided [RCV003729779]likely benign21004817110048171Humanname
405011117CV3128079single nucleotide variantNM_003597.5(KLF11):c.522C>T (p.Ser174=)not provided [RCV003828959]likely benign21004785910047859Humanname
405174430CV3150550single nucleotide variantNM_003597.5(KLF11):c.870C>A (p.Ile290=)not provided [RCV003841824]likely benign21004820710048207Humanname
405272929CV3197573single nucleotide variantNM_003597.5(KLF11):c.699C>T (p.Pro233=)KLF11-related disorder [RCV003901541]likely benign21004803610048036Humanname , trait , alternate_id
405273498CV3197849single nucleotide variantNM_003597.5(KLF11):c.35C>A (p.Ala12Glu)KLF11-related disorder [RCV003901812]|not provided [RCV005101541]uncertain significance21004375110043751Human1name , trait , alternate_id
405265136CV3202131single nucleotide variantNM_003597.5(KLF11):c.987C>T (p.Phe329=)KLF11-related disorder [RCV003897286]likely benign21004832410048324Humanname , trait , alternate_id
405289521CV3218265single nucleotide variantNM_003597.5(KLF11):c.684G>A (p.Leu228=)KLF11-related disorder [RCV003983667]likely benign21004802110048021Humanname , trait , alternate_id
597638980CV3692102single nucleotide variantNM_003597.5(KLF11):c.80G>A (p.Arg27Lys)not specified [RCV004941266]uncertain significance21004618710046187Humanname
597858996CV3755897single nucleotide variantNM_003597.5(KLF11):c.52A>G (p.Met18Val)not provided [RCV005089048]uncertain significance21004615910046159Humanname
597970229CV3791810single nucleotide variantNM_003597.5(KLF11):c.819C>T (p.Thr273=)not provided [RCV005141627]likely benign21004815610048156Humanname
597946587CV3817731single nucleotide variantNM_003597.5(KLF11):c.681C>T (p.Asn227=)not provided [RCV005160197]likely benign21004801810048018Humanname
597891763CV3840184single nucleotide variantNM_003597.5(KLF11):c.834C>G (p.Val278=)not provided [RCV005179883]likely benign21004817110048171Humanname
598161051CV3976590single nucleotide variantNM_003597.5(KLF11):c.40G>A (p.Ala14Thr)not specified [RCV005368360]uncertain significance21004375610043756Humanname
28877461CV880759single nucleotide variantNM_003597.5(KLF11):c.351A>G (p.Pro117=)KLF11-related disorder [RCV003963072]|Maturity-onset diabetes of the young type 7 [RCV001134795]likely benign|uncertain significance21004768810047688Human1name , trait , alternate_id
28868241CV880761single nucleotide variantNM_003597.5(KLF11):c.501C>T (p.Pro167=)Maturity-onset diabetes of the young type 7 [RCV001129809]uncertain significance21004783810047838Human1name
28872822CV880766single nucleotide variantNM_003597.5(KLF11):c.870C>T (p.Ile290=)Maturity-onset diabetes of the young type 7 [RCV001132500]|not specified [RCV004935188]likely benign21004820710048207Human1name
127318508CV1153772single nucleotide variantNM_003597.5(KLF11):c.1185A>T (p.Val395=)not provided [RCV001521689]benign21004852210048522Humanname
8659896CV134877single nucleotide variantNM_003597.5(KLF11):c.185A>G (p.Gln62Arg)Maturity-onset diabetes of the young type 7 [RCV000321050]|Type 2 diabetes mellitus [RCV002250563]|not provided [RCV001668243]|not specified [RCV000117438]likely risk allele|benign|likely benign|conflicting interpretations of pathogenicity|no classifications from unflagged records21004629210046292Human4name
151787584CV1416729single nucleotide variantNM_003597.5(KLF11):c.145G>A (p.Glu49Lys)not provided [RCV001989746]uncertain significance21004625210046252Humanname
151725098CV1437221single nucleotide variantNM_003597.5(KLF11):c.245C>A (p.Thr82Asn)not provided [RCV002004165]uncertain significance21004635210046352Humanname
152172310CV1599071single nucleotide variantNM_003597.5(KLF11):c.1050G>A (p.Pro350=)Maturity-onset diabetes of the young type 7 [RCV002505814]|not provided [RCV002143734]likely benign21004838710048387Human1name
156302234CV1926406single nucleotide variantNM_003597.5(KLF11):c.1041C>T (p.Ala347=)not provided [RCV002647701]benign21004837810048378Humanname
156409659CV1961892single nucleotide variantNM_003597.5(KLF11):c.1110C>T (p.Ala370=)not provided [RCV002586892]likely benign21004844710048447Humanname
156380531CV1964246single nucleotide variantNM_003597.5(KLF11):c.1314G>A (p.Ser438=)not provided [RCV002583136]likely benign21005228210052282Humanname
156115127CV2035456single nucleotide variantNM_003597.5(KLF11):c.275C>T (p.Pro92Leu)not provided [RCV002785559]uncertain significance21004638210046382Humanname
11577539CV281450single nucleotide variantNM_003597.5(KLF11):c.266C>T (p.Ala89Val)Maturity-onset diabetes of the young type 7 [RCV000262445]uncertain significance21004637310046373Human1name
401910860CV2815527single nucleotide variantNM_003597.5(KLF11):c.248C>T (p.Thr83Ile)not provided [RCV003425506]uncertain significance21004635510046355Humanname
11581187CV282108single nucleotide variantNM_003597.5(KLF11):c.259A>G (p.Met87Val)Maturity-onset diabetes of the young type 7 [RCV000359484]uncertain significance21004636610046366Human1name
405199536CV2877031single nucleotide variantNM_003597.5(KLF11):c.241G>A (p.Val81Ile)not provided [RCV003551248]uncertain significance21004634810046348Humanname
405241177CV2893067single nucleotide variantNM_003597.5(KLF11):c.1371G>A (p.Pro457=)KLF11-related disorder [RCV003946717]|not provided [RCV003557316]likely benign21005233910052339Human1name , trait , alternate_id
405090770CV2937385single nucleotide variantNM_003597.5(KLF11):c.274C>G (p.Pro92Ala)not provided [RCV003665267]uncertain significance21004638110046381Humanname
402489821CV2941701single nucleotide variantNM_003597.5(KLF11):c.1257A>G (p.Thr419=)not provided [RCV003660383]uncertain significance21004859410048594Humanname
405283478CV3202724single nucleotide variantNM_003597.5(KLF11):c.1083C>T (p.Ala361=)KLF11-related disorder [RCV003921829]|not provided [RCV005101701]likely benign21004842010048420Human1name , trait , alternate_id
405289634CV3220975single nucleotide variantNM_003597.5(KLF11):c.1131C>T (p.Thr377=)KLF11-related disorder [RCV003961872]likely benign21004846810048468Humanname , trait , alternate_id
405807502CV3265514single nucleotide variantNM_003597.5(KLF11):c.278A>G (p.Glu93Gly)not specified [RCV004406585]uncertain significance21004638510046385Humanname
407470114CV3452354single nucleotide variantNM_003597.5(KLF11):c.260T>G (p.Met87Arg)not specified [RCV004637034]uncertain significance21004636710046367Humanname
597945904CV3755461single nucleotide variantNM_003597.5(KLF11):c.1044C>G (p.Leu348=)not provided [RCV005078470]likely benign21004838110048381Humanname
597936148CV3759552single nucleotide variantNM_003597.5(KLF11):c.1473G>A (p.Lys491=)not provided [RCV005076672]likely benign21005244110052441Humanname
597940843CV3772785single nucleotide variantNM_003597.5(KLF11):c.1464G>A (p.Glu488=)not provided [RCV005118415]likely benign21005243210052432Humanname
597877358CV3813375single nucleotide variantNM_003597.5(KLF11):c.179G>A (p.Arg60Lys)not provided [RCV005149311]uncertain significance21004628610046286Humanname
597877803CV3813602single nucleotide variantNM_003597.5(KLF11):c.227C>T (p.Ser76Phe)not provided [RCV005149344]uncertain significance21004633410046334Humanname
597970837CV3832617single nucleotide variantNM_003597.5(KLF11):c.100A>G (p.Arg34Gly)not provided [RCV005166696]uncertain significance21004620710046207Humanname
597975917CV3832837single nucleotide variantNM_003597.5(KLF11):c.167C>T (p.Ser56Phe)not provided [RCV005169396]uncertain significance21004627410046274Humanname
597928303CV3837242single nucleotide variantNM_003597.5(KLF11):c.1410G>A (p.Thr470=)not provided [RCV005185400]likely benign21005237810052378Humanname
597922531CV3843266single nucleotide variantNM_003597.5(KLF11):c.203G>A (p.Arg68Gln)not provided [RCV005184558]uncertain significance21004631010046310Humanname
28877745CV880771single nucleotide variantNM_003597.5(KLF11):c.1161C>T (p.Asp387=)Maturity-onset diabetes of the young type 7 [RCV001134908]|not specified [RCV001819838]likely benign21004849810048498Human1name
28868363CV880776single nucleotide variantNM_003597.5(KLF11):c.1503G>A (p.Pro501=)Maturity-onset diabetes of the young type 7 [RCV001129893]|not provided [RCV002556828]likely benign21005247110052471Human1name
150434015CV1243846deletionNM_003597.5(KLF11):c.1258+333_1258+335delnot provided [RCV001665052]benign21004890910048911Humanname
150449685CV1254009deletionNM_003597.5(KLF11):c.1258+334_1258+335delnot provided [RCV001667646]benign21004890910048910Humanname
151355163CV1328230single nucleotide variantNM_003597.5(KLF11):c.811A>C (p.Lys271Gln)Maturity-onset diabetes of the young type 7 [RCV002503317]|not specified [RCV001820235]uncertain significance21004814810048148Human1name
8657594CV134876single nucleotide variantNM_003597.5(KLF11):c.410A>G (p.Asp137Gly)Monogenic diabetes [RCV000664078]|not provided [RCV000881038]|not specified [RCV000117437]benign|likely benign21004774710047747Human1name
8657595CV134878single nucleotide variantNM_003597.5(KLF11):c.467G>T (p.Gly156Val)not provided [RCV000117439]|not specified [RCV004935128]conflicting interpretations of pathogenicity|uncertain significance21004780410047804Humanname
151746446CV1365942single nucleotide variantNM_003597.5(KLF11):c.314G>T (p.Cys105Phe)not provided [RCV001893828]uncertain significance21004765110047651Humanname
151795323CV1470895single nucleotide variantNM_003597.5(KLF11):c.437C>T (p.Ala146Val)Maturity-onset diabetes of the young type 7 [RCV002507610]|not provided [RCV001952427]|not specified [RCV004041946]uncertain significance21004777410047774Human1name
151798377CV1480313single nucleotide variantNM_003597.5(KLF11):c.992G>T (p.Gly331Val)Maturity-onset diabetes of the young type 7 [RCV002507614]|not provided [RCV001952691]|not specified [RCV005350769]uncertain significance21004832910048329Human1name
151769272CV1481631single nucleotide variantNM_003597.5(KLF11):c.916C>A (p.Pro306Thr)not provided [RCV002008688]uncertain significance21004825310048253Humanname
153000859CV1683858single nucleotide variantNM_003597.5(KLF11):c.914C>T (p.Pro305Leu)not provided [RCV002254477]uncertain significance21004825110048251Humanname
155641689CV1709907single nucleotide variantNM_003597.5(KLF11):c.929C>T (p.Ser310Phe)not provided [RCV002293007]likely benign21004826610048266Humanname
156229132CV1888900single nucleotide variantNM_003597.5(KLF11):c.353C>T (p.Ser118Leu)not provided [RCV003085293]uncertain significance21004769010047690Humanname
156020652CV1909494single nucleotide variantNM_003597.5(KLF11):c.727C>G (p.Leu243Val)not provided [RCV002619376]uncertain significance21004806410048064Humanname
156385450CV1990094single nucleotide variantNM_003597.5(KLF11):c.940G>C (p.Val314Leu)not provided [RCV002634583]|not specified [RCV004065797]uncertain significance21004827710048277Humanname
156010714CV1991847single nucleotide variantNM_003597.5(KLF11):c.523G>A (p.Val175Met)not provided [RCV002626799]|not specified [RCV004065937]uncertain significance21004786010047860Humanname
156119899CV2039386single nucleotide variantNM_003597.5(KLF11):c.793G>A (p.Glu265Lys)not provided [RCV002800183]uncertain significance21004813010048130Humanname
156016555CV2044100single nucleotide variantNM_003597.5(KLF11):c.407C>T (p.Thr136Met)not provided [RCV002795376]uncertain significance21004774410047744Humanname
155961420CV2138415single nucleotide variantNM_003597.5(KLF11):c.758C>G (p.Pro253Arg)not provided [RCV002972404]uncertain significance21004809510048095Humanname
8559374CV21538single nucleotide variantNM_003597.5(KLF11):c.659C>T (p.Thr220Met)Maturity-onset diabetes of the young type 7 [RCV000006872]|Monogenic diabetes [RCV000445442]|not provided [RCV000429958]|not specified [RCV000247830]pathogenic|benign|likely benign21004799610047996Human2name
156256797CV2159253single nucleotide variantNM_003597.5(KLF11):c.842C>G (p.Pro281Arg)not provided [RCV003026528]uncertain significance21004817910048179Humanname
155998109CV2168856single nucleotide variantNM_003597.5(KLF11):c.650C>T (p.Thr217Ile)KLF11-related disorder [RCV003410033]|not provided [RCV003017146]uncertain significance21004798710047987Human1name , trait , alternate_id
156347465CV2172763single nucleotide variantNM_003597.5(KLF11):c.428C>T (p.Ala143Val)not provided [RCV003030637]uncertain significance21004776510047765Humanname
156196223CV2241528single nucleotide variantNM_003597.5(KLF11):c.451G>C (p.Gly151Arg)not specified [RCV004104427]likely benign21004778810047788Humanname
155907099CV2302150single nucleotide variantNM_003597.5(KLF11):c.754T>C (p.Trp252Arg)not specified [RCV004159164]uncertain significance21004809110048091Humanname
156242264CV2306502single nucleotide variantNM_003597.5(KLF11):c.630C>G (p.His210Gln)not specified [RCV004157118]uncertain significance21004796710047967Humanname
156154723CV2314237single nucleotide variantNM_003597.5(KLF11):c.350C>T (p.Pro117Leu)not specified [RCV004166605]uncertain significance21004768710047687Humanname
156163262CV2323597single nucleotide variantNM_003597.5(KLF11):c.422C>T (p.Ser141Phe)not specified [RCV004165787]uncertain significance21004775910047759Humanname
156355728CV2324536single nucleotide variantNM_003597.5(KLF11):c.655C>G (p.Leu219Val)not specified [RCV004179012]uncertain significance21004799210047992Humanname
155918806CV2360077single nucleotide variantNM_003597.5(KLF11):c.458C>T (p.Ala153Val)not specified [RCV004215358]uncertain significance21004779510047795Humanname
155937687CV2380065single nucleotide variantNM_003597.5(KLF11):c.938C>T (p.Thr313Ile)not provided [RCV005099082]|not specified [RCV004222194]uncertain significance21004827510048275Humanname
329362082CV2456720single nucleotide variantNM_003597.5(KLF11):c.412G>A (p.Val138Ile)not specified [RCV004277886]likely benign21004774910047749Humanname
401829994CV2747727single nucleotide variantNM_003597.5(KLF11):c.308C>T (p.Thr103Ile)Maturity-onset diabetes of the young type 7 [RCV003329145]uncertain significance21004641510046415Human1name
401935003CV2798097duplicationNM_003597.5(KLF11):c.1059dup (p.Cys354fs)KLF11-related disorder [RCV003412419]uncertain significance21004839110048392Humanname , trait , alternate_id
11578996CV281454single nucleotide variantNM_003597.5(KLF11):c.679A>G (p.Asn227Asp)Maturity-onset diabetes of the young type 7 [RCV000293457]likely benign|uncertain significance21004801610048016Human1name
11580840CV281457single nucleotide variantNM_003597.5(KLF11):c.689C>T (p.Ser230Phe)Maturity-onset diabetes of the young type 7 [RCV000345993]uncertain significance21004802610048026Human1name
11581516CV282110single nucleotide variantNM_003597.5(KLF11):c.358A>G (p.Arg120Gly)Maturity-onset diabetes of the young type 7 [RCV000372911]uncertain significance21004769510047695Human1name
11580815CV282114single nucleotide variantNM_003597.5(KLF11):c.994C>T (p.Pro332Ser)Maturity-onset diabetes of the young type 7 [RCV000345253]uncertain significance21004833110048331Human1name
11580020CV283452single nucleotide variantNM_003597.5(KLF11):c.305C>G (p.Ser102Trp)Maturity-onset diabetes of the young type 7 [RCV000319853]uncertain significance21004641210046412Human1name
11578710CV283456single nucleotide variantNM_003597.5(KLF11):c.928T>C (p.Ser310Pro)Maturity-onset diabetes of the young type 7 [RCV000287486]uncertain significance21004826510048265Human1name
11581786CV283576single nucleotide variantNM_003597.5(KLF11):c.782C>T (p.Pro261Leu)Maturity-onset diabetes of the young type 7 [RCV000384196]|Monogenic diabetes [RCV000664079]|not provided [RCV001850772]|not specified [RCV000500248]benign|likely benign21004811910048119Human2name
405013381CV2933958single nucleotide variantNM_003597.5(KLF11):c.508G>A (p.Ala170Thr)not provided [RCV003576868]uncertain significance21004784510047845Humanname
405116373CV3020127single nucleotide variantNM_003597.5(KLF11):c.518C>G (p.Thr173Ser)not provided [RCV003700284]uncertain significance21004785510047855Humanname
405246248CV3048012single nucleotide variantNM_003597.5(KLF11):c.487G>C (p.Val163Leu)not provided [RCV003720499]uncertain significance21004782410047824Humanname
405186879CV3058602single nucleotide variantNM_003597.5(KLF11):c.643C>A (p.Gln215Lys)Maturity-onset diabetes of the young type 7 [RCV005392682]|not provided [RCV003729250]uncertain significance21004798010047980Human1name
405182057CV3120025single nucleotide variantNM_003597.5(KLF11):c.950T>C (p.Ile317Thr)not provided [RCV003820119]uncertain significance21004828710048287Humanname
404987341CV3179760single nucleotide variantNM_003597.5(KLF11):c.574A>G (p.Thr192Ala)not provided [RCV003881237]uncertain significance21004791110047911Humanname
405807504CV3265515single nucleotide variantNM_003597.5(KLF11):c.587G>A (p.Arg196Gln)not specified [RCV004406586]likely benign21004792410047924Humanname
405807506CV3265516single nucleotide variantNM_003597.5(KLF11):c.899C>T (p.Pro300Leu)not specified [RCV004406587]uncertain significance21004823610048236Humanname
405807508CV3265517single nucleotide variantNM_003597.5(KLF11):c.917C>T (p.Pro306Leu)not specified [RCV004406588]uncertain significance21004825410048254Humanname
407524887CV3452355single nucleotide variantNM_003597.5(KLF11):c.503G>C (p.Cys168Ser)not specified [RCV004631529]uncertain significance21004784010047840Humanname
407470119CV3452356single nucleotide variantNM_003597.5(KLF11):c.850C>T (p.Pro284Ser)not specified [RCV004637035]uncertain significance21004818710048187Humanname
597638974CV3692100single nucleotide variantNM_003597.5(KLF11):c.851C>T (p.Pro284Leu)not specified [RCV004941265]uncertain significance21004818810048188Humanname
597946598CV3755617single nucleotide variantNM_003597.5(KLF11):c.648C>A (p.Asp216Glu)not provided [RCV005078627]uncertain significance21004798510047985Humanname
597909285CV3781986single nucleotide variantNM_003597.5(KLF11):c.850C>G (p.Pro284Ala)not provided [RCV005128478]uncertain significance21004818710048187Humanname
12848590CV380187single nucleotide variantNM_003597.5(KLF11):c.541G>A (p.Glu181Lys)KLF11-related disorder [RCV003942464]|Maturity-onset diabetes of the young type 7 [RCV002502592]|Monogenic diabetes [RCV000445489]|not provided [RCV002063658]|not specified [RCV001821212]benign|likely benign21004787810047878Human2name , trait , alternate_id
12848594CV380188single nucleotide variantNM_003597.5(KLF11):c.953T>G (p.Leu318Arg)Maturity-onset diabetes of the young type 7 [RCV001133425]|Monogenic diabetes [RCV000445493]|not provided [RCV003546563]likely benign|uncertain significance21004829010048290Human2name
597862364CV3822651single nucleotide variantNM_003597.5(KLF11):c.827T>C (p.Ile276Thr)not provided [RCV005175182]uncertain significance21004816410048164Humanname
598220928CV3976591single nucleotide variantNM_003597.5(KLF11):c.851C>A (p.Pro284His)not specified [RCV005360737]uncertain significance21004818810048188Humanname
598182255CV3976592single nucleotide variantNM_003597.5(KLF11):c.415C>T (p.Leu139Phe)not specified [RCV005352704]uncertain significance21004775210047752Humanname
598200005CV4007388single nucleotide variantNM_003597.5(KLF11):c.343G>C (p.Val115Leu)Maturity-onset diabetes of the young type 7 [RCV005398216]uncertain significance21004768010047680Human1name
13216535CV427870single nucleotide variantNM_003597.5(KLF11):c.871C>T (p.Pro291Ser)not specified [RCV000503793]uncertain significance21004820810048208Humanname
8629752CV84899single nucleotide variantNM_003597.4(KLF11):c.856C>T (p.Leu286Phe)Malignant melanoma [RCV000064981]not provided21004819310048193Humanname
28868236CV880760single nucleotide variantNM_003597.5(KLF11):c.431T>C (p.Val144Ala)Maturity-onset diabetes of the young type 7 [RCV001129808]uncertain significance21004776810047768Human1name
28868243CV880762single nucleotide variantNM_003597.5(KLF11):c.546C>A (p.Ser182Arg)Maturity-onset diabetes of the young type 7 [RCV001129810]|not provided [RCV001873521]likely benign|uncertain significance21004788310047883Human1name
28868245CV880763single nucleotide variantNM_003597.5(KLF11):c.608G>A (p.Gly203Glu)Maturity-onset diabetes of the young type 7 [RCV001129811]|not provided [RCV001873522]uncertain significance21004794510047945Human1name
28868247CV880764single nucleotide variantNM_003597.5(KLF11):c.644A>G (p.Gln215Arg)Maturity-onset diabetes of the young type 7 [RCV001129812]uncertain significance21004798110047981Human1name
28872820CV880765single nucleotide variantNM_003597.5(KLF11):c.673A>C (p.Ser225Arg)Maturity-onset diabetes of the young type 7 [RCV001132499]|not provided [RCV003718348]|not specified [RCV001819837]uncertain significance21004801010048010Human1name
28872825CV880767single nucleotide variantNM_003597.5(KLF11):c.926T>C (p.Leu309Ser)Maturity-onset diabetes of the young type 7 [RCV001132501]uncertain significance21004826310048263Human1name
28874490CV880768single nucleotide variantNM_003597.5(KLF11):c.961G>C (p.Ala321Pro)Maturity-onset diabetes of the young type 7 [RCV001133426]uncertain significance21004829810048298Human1name
126911727CV1037064single nucleotide variantNM_003597.5(KLF11):c.1246C>T (p.Arg416Cys)not provided [RCV001355687]uncertain significance21004858310048583Humanname
151354777CV1327844single nucleotide variantNM_003597.5(KLF11):c.1396A>T (p.Ser466Cys)Maturity-onset diabetes of the young type 7 [RCV002482360]|not provided [RCV003718438]|not specified [RCV001819319]uncertain significance21005236410052364Human1name
151726784CV1353051single nucleotide variantNM_003597.5(KLF11):c.1310G>T (p.Arg437Leu)not provided [RCV001891820]uncertain significance21005227810052278Humanname
151853088CV1376220single nucleotide variantNM_003597.5(KLF11):c.1037G>T (p.Gly346Val)Maturity-onset diabetes of the young type 7 [RCV002492301]|not provided [RCV001996209]uncertain significance21004837410048374Human1name
151749159CV1380851single nucleotide variantNM_003597.5(KLF11):c.1054G>A (p.Ala352Thr)not provided [RCV002023194]uncertain significance21004839110048391Humanname
156258187CV1906364single nucleotide variantNM_003597.5(KLF11):c.1382G>A (p.Arg461Gln)KLF11-related disorder [RCV003943788]|not provided [RCV003086345]likely benign21005235010052350Human1name , trait , alternate_id
156288074CV1964735single nucleotide variantNM_003597.5(KLF11):c.1447C>T (p.Pro483Ser)not provided [RCV002577719]uncertain significance21005241510052415Humanname
156314689CV2031816single nucleotide variantNM_003597.5(KLF11):c.1390A>G (p.Met464Val)not provided [RCV002716733]uncertain significance21005235810052358Humanname
156321802CV2123863single nucleotide variantNM_003597.5(KLF11):c.1298A>G (p.Lys433Arg)KLF11-related disorder [RCV004750232]|not provided [RCV002963256]uncertain significance21005226610052266Human1name , trait , alternate_id
8559373CV21537single nucleotide variantNM_003597.5(KLF11):c.1039G>T (p.Ala347Ser)Maturity-onset diabetes of the young type 7 [RCV000006871]|not provided [RCV002512855]pathogenic|likely benign|conflicting interpretations of pathogenicity|uncertain significance21004837610048376Human1name
156053633CV2385609single nucleotide variantNM_003597.5(KLF11):c.1313C>T (p.Ser438Leu)not specified [RCV004233244]uncertain significance21005228110052281Humanname
329357008CV2431220single nucleotide variantNM_003597.5(KLF11):c.1252C>T (p.His418Tyr)not specified [RCV004250562]uncertain significance21004858910048589Humanname
329371866CV2454962single nucleotide variantNM_003597.5(KLF11):c.1504G>A (p.Gly502Arg)not specified [RCV004272236]uncertain significance21005247210052472Humanname
401749880CV2704766single nucleotide variantNM_003597.5(KLF11):c.1144T>C (p.Cys382Arg)not provided [RCV003779956]|not specified [RCV004307361]uncertain significance21004848110048481Humanname
401867291CV2748861single nucleotide variantNM_003597.5(KLF11):c.1070A>G (p.Asn357Ser)not provided [RCV003549060]|not specified [RCV003331683]likely benign21004840710048407Humanname
401861305CV2779610single nucleotide variantNM_003597.5(KLF11):c.1348G>A (p.Gly450Arg)not specified [RCV004351317]uncertain significance21005231610052316Humanname
401868308CV2781473single nucleotide variantNM_003597.5(KLF11):c.1457A>G (p.Gln486Arg)not specified [RCV004354709]uncertain significance21005242510052425Humanname
401907261CV2802328single nucleotide variantNM_003597.5(KLF11):c.1039G>A (p.Ala347Thr)KLF11-related disorder [RCV003422512]uncertain significance21004837610048376Humanname , trait , alternate_id
401936447CV2803530single nucleotide variantNM_003597.5(KLF11):c.1302G>C (p.Lys434Asn)KLF11-related disorder [RCV003414458]|not provided [RCV003553899]uncertain significance21005227010052270Human1name , trait , alternate_id
11580630CV281461single nucleotide variantNM_003597.5(KLF11):c.1077G>A (p.Met359Ile)Diabetes mellitus [RCV001172531]|Maturity-onset diabetes of the young type 7 [RCV000339444]|not provided [RCV001850773]uncertain significance21004841410048414Human3name
401910861CV2815528single nucleotide variantNM_003597.5(KLF11):c.1421G>A (p.Arg474Gln)not provided [RCV003425507]uncertain significance21005238910052389Humanname
11652550CV282116single nucleotide variantNM_003597.5(KLF11):c.1057C>A (p.Pro353Thr)Maturity-onset diabetes of the young type 7 [RCV000305609]uncertain significance21004839410048394Human1name
11663882CV283457single nucleotide variantNM_003597.5(KLF11):c.1046C>T (p.Pro349Leu)Maturity-onset diabetes of the young type 7 [RCV000400205]uncertain significance21004838310048383Human1name
11581123CV283465single nucleotide variantNM_003597.5(KLF11):c.1169G>A (p.Arg390Gln)Maturity-onset diabetes of the young type 7 [RCV000356724]|not provided [RCV005090513]uncertain significance21004850610048506Human1name
11582322CV283588single nucleotide variantNM_003597.5(KLF11):c.1102C>T (p.Pro368Ser)Maturity-onset diabetes of the young type 7 [RCV000407600]|not provided [RCV005090512]uncertain significance21004843910048439Human1name
11579278CV283601single nucleotide variantNM_003597.5(KLF11):c.1137C>G (p.Ser379Arg)Maturity-onset diabetes of the young type 7 [RCV000299545]|not provided [RCV002057557]|not specified [RCV004021761]likely benign|uncertain significance21004847410048474Human1name
11577406CV283602single nucleotide variantNM_003597.5(KLF11):c.1448C>T (p.Pro483Leu)Maturity-onset diabetes of the young type 7 [RCV000259648]|not specified [RCV003317193]benign|likely benign|uncertain significance21005241610052416Human1name
405236169CV2887867single nucleotide variantNM_003597.5(KLF11):c.1429A>G (p.Met477Val)KLF11-related disorder [RCV003946691]|not provided [RCV003556429]likely benign21005239710052397Human1name , trait , alternate_id
405044782CV3074400single nucleotide variantNM_003597.5(KLF11):c.1502C>T (p.Pro501Leu)not provided [RCV003740180]uncertain significance21005247010052470Humanname
405807495CV3265510single nucleotide variantNM_003597.5(KLF11):c.1117C>G (p.Pro373Ala)Maturity-onset diabetes of the young type 7 [RCV005023522]|not specified [RCV004406581]uncertain significance21004845410048454Human1name
405807497CV3265511single nucleotide variantNM_003597.5(KLF11):c.1118C>T (p.Pro373Leu)not specified [RCV004406582]uncertain significance21004845510048455Humanname
405807498CV3265512single nucleotide variantNM_003597.5(KLF11):c.1249A>G (p.Thr417Ala)not specified [RCV004406583]uncertain significance21004858610048586Humanname
405807500CV3265513single nucleotide variantNM_003597.5(KLF11):c.1393C>T (p.Arg465Cys)not specified [RCV004406584]uncertain significance21005236110052361Humanname
597638968CV3692099single nucleotide variantNM_003597.5(KLF11):c.1423C>T (p.Arg475Cys)not specified [RCV004941264]uncertain significance21005239110052391Humanname
597768491CV3692101single nucleotide variantNM_003597.5(KLF11):c.1327C>T (p.Arg443Cys)not specified [RCV004927499]uncertain significance21005229510052295Humanname
597752031CV3705934single nucleotide variantNM_003597.5(KLF11):c.1120G>A (p.Val374Met)Maturity-onset diabetes of the young type 7 [RCV005015974]uncertain significance21004845710048457Human1name
597934302CV3750455single nucleotide variantNM_003597.5(KLF11):c.1526C>G (p.Pro509Arg)not provided [RCV005076380]uncertain significance21005249410052494Humanname
597899389CV3782882single nucleotide variantNM_003597.5(KLF11):c.1151C>G (p.Pro384Arg)not provided [RCV005126902]uncertain significance21004848810048488Humanname
12848531CV380189single nucleotide variantNM_003597.5(KLF11):c.1205G>A (p.Arg402Gln)KLF11-related disorder [RCV003912785]|Maturity-onset diabetes of the young type 7 [RCV001134909]|Monogenic diabetes [RCV000445374]|not provided [RCV003698790]benign|likely benign21004854210048542Human2name , trait , alternate_id
597906008CV3804014single nucleotide variantNM_003597.5(KLF11):c.1048C>T (p.Pro350Ser)not provided [RCV005153560]likely benign21004838510048385Humanname
597856068CV3822089single nucleotide variantNM_003597.5(KLF11):c.1247G>T (p.Arg416Leu)not provided [RCV005174387]uncertain significance21004858410048584Humanname
597875552CV3829704single nucleotide variantNM_003597.5(KLF11):c.1471A>G (p.Lys491Glu)not provided [RCV005177412]uncertain significance21005243910052439Humanname
597973909CV3831133single nucleotide variantNM_003597.5(KLF11):c.1272C>G (p.Phe424Leu)not provided [RCV005168271]uncertain significance21005224010052240Humanname
598161045CV3976589single nucleotide variantNM_003597.5(KLF11):c.1204C>T (p.Arg402Trp)not specified [RCV005368359]uncertain significance21004854110048541Humanname
28874494CV880769single nucleotide variantNM_003597.5(KLF11):c.1049C>T (p.Pro350Leu)Maturity-onset diabetes of the young type 7 [RCV001133427]uncertain significance21004838610048386Human1name
28877741CV880770single nucleotide variantNM_003597.5(KLF11):c.1130C>T (p.Thr377Ile)Maturity-onset diabetes of the young type 7 [RCV001134907]|not provided [RCV001856725]likely benign|uncertain significance21004846710048467Human1name
28877753CV880772single nucleotide variantNM_003597.5(KLF11):c.1304T>A (p.Phe435Tyr)Maturity-onset diabetes of the young type 7 [RCV001134910]|not provided [RCV002070576]likely benign|uncertain significance21005227210052272Human1name
28868356CV880773single nucleotide variantNM_003597.5(KLF11):c.1396A>G (p.Ser466Gly)Maturity-onset diabetes of the young type 7 [RCV001129890]uncertain significance21005236410052364Human1name
28868357CV880774single nucleotide variantNM_003597.5(KLF11):c.1450G>A (p.Gly484Ser)Maturity-onset diabetes of the young type 7 [RCV001129891]benign21005241810052418Human1name
28868360CV880775single nucleotide variantNM_003597.5(KLF11):c.1486G>A (p.Ala496Thr)Maturity-onset diabetes of the young type 7 [RCV001129892]|not specified [RCV004032284]likely benign|uncertain significance21005245410052454Human1name
405238097CV2881218microsatelliteNM_003597.5(KLF11):c.1354AAG[1] (p.Lys453del)not provided [RCV003556707]uncertain significance21005232010052322Humanname
597835174CV3760917deletionNM_003597.5(KLF11):c.1347_1348del (p.Lys452fs)not provided [RCV005085468]uncertain significance21005231510052316Humanname
597848536CV3736841deletionNM_003597.5(KLF11):c.1411_1413del (p.Lys471del)not provided [RCV005066000]uncertain significance21005237810052380Humanname
12848529CV380181indelNM_003597.5(KLF11):c.608_609delinsAG (p.Gly203Glu)Monogenic diabetes [RCV000445371]|not provided [RCV003727735]uncertain significance21004794510047946Humanname