ClinVar Miner

List of variants in gene FKBP10 reported as uncertain significance for bone development disease

Included ClinVar conditions (614):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP gnomAD frequency
NM_021939.4(FKBP10):c.590A>G (p.Lys197Arg) rs34764749 0.06739
NM_021939.4(FKBP10):c.917+53G>T rs141387386 0.00927
NM_021939.3(FKBP10):c.-177C>G rs555053677 0.00160
NM_021939.4(FKBP10):c.1137G>A (p.Val379=) rs116142981 0.00150
NM_021939.4(FKBP10):c.1667G>A (p.Arg556His) rs138281924 0.00120
NM_021939.4(FKBP10):c.1256C>T (p.Ser419Leu) rs146422412 0.00107
NM_021939.4(FKBP10):c.1363A>G (p.Ile455Val) rs146701946 0.00098
NM_021939.4(FKBP10):c.1290C>T (p.Leu430=) rs143450797 0.00044
NM_021939.4(FKBP10):c.*549G>A rs757353571 0.00043
NM_021939.3(FKBP10):c.-183C>G rs533813401 0.00036
NM_021939.3(FKBP10):c.-207C>T rs782363137 0.00026
NM_021939.4(FKBP10):c.*508G>A rs1022964355 0.00024
NM_021939.4(FKBP10):c.491C>T (p.Pro164Leu) rs117897485 0.00023
NM_021939.4(FKBP10):c.850G>A (p.Gly284Arg) rs372214186 0.00023
NM_021939.4(FKBP10):c.*693G>T rs886052927 0.00013
NM_021939.4(FKBP10):c.*589T>C rs886052925 0.00010
NM_021939.4(FKBP10):c.616G>A (p.Gly206Ser) rs146440863 0.00010
NM_021939.4(FKBP10):c.473T>C (p.Val158Ala) rs781874365 0.00009
NM_021939.4(FKBP10):c.1003A>G (p.Met335Val) rs369599375 0.00008
NM_021939.4(FKBP10):c.520G>A (p.Gly174Ser) rs140950528 0.00008
NM_021939.4(FKBP10):c.677G>A (p.Arg226Lys) rs556997852 0.00008
NM_021939.4(FKBP10):c.1556C>T (p.Pro519Leu) rs140883152 0.00007
NM_021939.4(FKBP10):c.268G>A (p.Ala90Thr) rs1242462441 0.00006
NM_021939.4(FKBP10):c.309C>T (p.Asp103=) rs199576301 0.00006
NM_021939.4(FKBP10):c.1366G>A (p.Val456Met) rs782275233 0.00004
NM_021939.4(FKBP10):c.1402C>T (p.Arg468Trp) rs542334549 0.00004
NM_021939.4(FKBP10):c.917+5G>A rs782117189 0.00004
NM_021939.4(FKBP10):c.942T>C (p.Asn314=) rs376553350 0.00004
NM_021939.4(FKBP10):c.1693G>A (p.Asp565Asn) rs201944190 0.00003
NM_021939.3(FKBP10):c.-303G>A rs886052922 0.00002
NM_021939.4(FKBP10):c.1323G>A (p.Thr441=) rs782332252 0.00002
NM_021939.4(FKBP10):c.1454G>A (p.Arg485Gln) rs144314381 0.00002
NM_021939.4(FKBP10):c.402T>G (p.Ile134Met) rs367689167 0.00002
NM_021939.4(FKBP10):c.408G>A (p.Pro136=) rs781784785 0.00002
NM_021939.4(FKBP10):c.587G>A (p.Ser196Asn) rs782660556 0.00002
NM_021939.4(FKBP10):c.792G>A (p.Pro264=) rs782789538 0.00002
NM_021939.4(FKBP10):c.984G>A (p.Gln328=) rs566306530 0.00002
NM_021939.3(FKBP10):c.-89G>A rs1325703846 0.00001
NM_021939.4(FKBP10):c.*760G>A rs910186954 0.00001
NM_021939.4(FKBP10):c.100G>A (p.Ala34Thr) rs1367029793 0.00001
NM_021939.4(FKBP10):c.1098C>T (p.Phe366=) rs886052923 0.00001
NM_021939.4(FKBP10):c.1286C>T (p.Thr429Ile) rs782547176 0.00001
NM_021939.4(FKBP10):c.1308C>T (p.Ile436=) rs782781776 0.00001
NM_021939.4(FKBP10):c.1613T>C (p.Met538Thr) rs144237565 0.00001
NM_021939.4(FKBP10):c.1723G>A (p.Glu575Lys) rs782264908 0.00001
NM_021939.4(FKBP10):c.393G>A (p.Ala131=) rs573350587 0.00001
NM_021939.4(FKBP10):c.522C>T (p.Gly174=) rs782350228 0.00001
NM_021939.4(FKBP10):c.573C>T (p.Phe191=) rs577264401 0.00001
NM_021939.4(FKBP10):c.591G>A (p.Lys197=) rs782308119 0.00001
NM_021939.4(FKBP10):c.915C>T (p.Ser305=) rs781996509 0.00001
NM_021939.3(FKBP10):c.-271G>C rs2047762029
NM_021939.3(FKBP10):c.-35C>A rs2047765734
NM_021939.4(FKBP10):c.*125C>T rs2047906187
NM_021939.4(FKBP10):c.*197T>A rs2047907188
NM_021939.4(FKBP10):c.*293G>A rs2047907943
NM_021939.4(FKBP10):c.*747C>T rs2047913178
NM_021939.4(FKBP10):c.1029C>G (p.Ile343Met) rs782632205
NM_021939.4(FKBP10):c.1256+11G>A rs199627092
NM_021939.4(FKBP10):c.1256+11G>T rs199627092
NM_021939.4(FKBP10):c.1256+17del rs55720039
NM_021939.4(FKBP10):c.1367T>C (p.Val456Ala) rs2047885191
NM_021939.4(FKBP10):c.1382C>T (p.Ala461Val) rs782004558
NM_021939.4(FKBP10):c.1400-6C>T rs782331462
NM_021939.4(FKBP10):c.1403G>A (p.Arg468Gln) rs1555617122
NM_021939.4(FKBP10):c.1522G>A (p.Asp508Asn) rs1597910363
NM_021939.4(FKBP10):c.21C>T (p.Pro7=) rs781985978
NM_021939.4(FKBP10):c.246-5C>G rs140027863
NM_021939.4(FKBP10):c.385G>A (p.Gly129Ser)
NM_021939.4(FKBP10):c.505C>G (p.Arg169Gly) rs782676847
NM_021939.4(FKBP10):c.773T>G (p.Leu258Arg) rs1597907453
NM_021939.4(FKBP10):c.825C>A (p.Leu275=) rs782638955
NM_021939.4(FKBP10):c.829C>G (p.Pro277Ala) rs138089753

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