ClinVar Miner

List of variants in gene TAF15 reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP gnomAD frequency
NM_139215.3(TAF15):c.783+320G>A rs4239252 0.31279
NM_139215.3(TAF15):c.48-210C>A rs4251737 0.15874
NM_139215.3(TAF15):c.1287A>G (p.Gly429=) rs4251785 0.15196
NM_139215.3(TAF15):c.914-216G>A rs9894083 0.10233
NM_139215.3(TAF15):c.1524C>T (p.Tyr508=) rs4251786 0.09533
NM_139215.3(TAF15):c.606-147C>T rs3785764 0.09146
NM_139215.3(TAF15):c.485-178G>C rs4251752 0.09125
NM_139215.3(TAF15):c.8-260A>G rs7209512 0.05358
NM_139215.3(TAF15):c.783+152T>A rs4251766 0.03927
NM_139215.3(TAF15):c.641-289G>A rs79909998 0.03058
NM_139215.3(TAF15):c.7+288G>A rs117281993 0.02997
NM_139215.3(TAF15):c.485-107G>A rs4251753 0.02519
NM_139215.3(TAF15):c.674-294C>A rs76549486 0.02130
NM_139215.3(TAF15):c.291-84G>A rs4251745 0.01868
NM_139215.3(TAF15):c.1178-29G>A rs4251784 0.01562
NM_139215.3(TAF15):c.1088+60A>G rs4251781 0.01503
NM_139215.3(TAF15):c.913+37G>T rs4251772 0.01090
NM_139215.3(TAF15):c.290+157G>A rs4251738 0.01066
NM_139215.3(TAF15):c.673+257C>A rs141462616 0.00950
NM_139215.3(TAF15):c.8-202A>G rs74398279 0.00864
NM_139215.3(TAF15):c.1089-25G>A rs4251782 0.00857
NM_139215.3(TAF15):c.641-29T>C rs112407824 0.00846
NM_139215.3(TAF15):c.641-50T>C rs201041043 0.00775
NM_139215.3(TAF15):c.1446T>C (p.Asp482=) rs144910879 0.00604
NM_139215.3(TAF15):c.485-4G>C rs4251755 0.00431
NM_139215.3(TAF15):c.1359T>C (p.Gly453=) rs1301559653 0.00197
NM_139215.3(TAF15):c.290+106A>T rs998078616 0.00143
NM_139215.3(TAF15):c.185-16C>T rs147370557 0.00117
NM_139215.3(TAF15):c.660C>T (p.Pro220=) rs138790468 0.00088
NM_139215.3(TAF15):c.726G>A (p.Gly242=) rs144851351 0.00087
NM_139215.3(TAF15):c.154G>A (p.Gly52Ser) rs117677306 0.00076
NM_139215.3(TAF15):c.876C>T (p.Asp292=) rs149293057 0.00076
NM_139215.3(TAF15):c.1332C>T (p.Gly444=) rs150034643 0.00066
NM_139215.3(TAF15):c.1163G>A (p.Arg388His) rs140268553 0.00056
NM_139215.3(TAF15):c.1184G>A (p.Arg395Gln) rs71381481 0.00011
NM_139215.3(TAF15):c.1344A>G (p.Gly448=) rs1321826060 0.00010
NM_139215.3(TAF15):c.1364A>G (p.Tyr455Cys) rs560923327 0.00008
NM_139215.3(TAF15):c.1388A>G (p.Tyr463Cys) rs756351856 0.00007
NM_139215.3(TAF15):c.1418G>A (p.Gly473Glu) rs777993379 0.00004
NM_139215.3(TAF15):c.1172G>A (p.Gly391Glu) rs375783267 0.00003
NM_139215.3(TAF15):c.446A>G (p.Tyr149Cys) rs755949830 0.00002
NM_139215.3(TAF15):c.436C>A (p.Gln146Lys) rs762891086 0.00001
NC_000017.11:g.35809264del rs3837828
NM_139215.3(TAF15):c.1151C>G (p.Pro384Arg)
NM_139215.3(TAF15):c.1269_1295dup (p.Gly424_Ser432dup) rs1440860624
NM_139215.3(TAF15):c.1287_1370del (p.Ser432_Arg459del) rs1568282429
NM_139215.3(TAF15):c.1320_1346del (p.442SGGGYGGDR[1]) rs1410671928
NM_139215.3(TAF15):c.1331G>A (p.Gly444Asp) rs1468873515
NM_139215.3(TAF15):c.1332_1358del (p.442SGGGYGGDR[1]) rs749600689
NM_139215.3(TAF15):c.1332_1358dup (p.Arg459_Gly460insSerGlyGlyGlyTyrGlyGlyAspArg) rs749600689
NM_139215.3(TAF15):c.1338_1341delinsCAGC (p.Gly447Ser)
NM_139215.3(TAF15):c.1344_1370dup (p.442SGGGYGGDR[3]) rs779360454
NM_139215.3(TAF15):c.1351_1377del (p.442SGGGYGGDR[1]) rs745996982
NM_139215.3(TAF15):c.1358G>T (p.Gly453Val) rs770549195
NM_139215.3(TAF15):c.1380_1403del (p.454GYGGDRGG[3]) rs768749438
NM_139215.3(TAF15):c.1392_1415del (p.454_461GYGGDRGG[3]) rs762946549
NM_139215.3(TAF15):c.1392_1415dup (p.454GYGGDRGG[5]) rs762946549
NM_139215.3(TAF15):c.1422_1445del (p.454_461GYGGDRGG[3]) rs779199064
NM_139215.3(TAF15):c.1428_1472del (p.478GYGGDRGGYGGDRGG[1]) rs750957958
NM_139215.3(TAF15):c.143A>G (p.Gln48Arg) rs2087242457
NM_139215.3(TAF15):c.1524_1544del (p.492GGYGGDR[4]) rs760281454
NM_139215.3(TAF15):c.1524_1544dup (p.492GGYGGDR[6]) rs760281454
NM_139215.3(TAF15):c.1542_1562del (p.492GGYGGDR[4]) rs750774088
NM_139215.3(TAF15):c.1651G>A (p.Gly551Arg)
NM_139215.3(TAF15):c.223C>G (p.Gln75Glu) rs2087244627
NM_139215.3(TAF15):c.227G>T (p.Ser76Ile) rs929675313
NM_139215.3(TAF15):c.290+105del rs879823976
NM_139215.3(TAF15):c.291-142A>G rs4251744
NM_139215.3(TAF15):c.291-278del rs909362495
NM_139215.3(TAF15):c.291-278dup rs909362495
NM_139215.3(TAF15):c.59A>G (p.Tyr20Cys)
NM_139215.3(TAF15):c.605+57dup rs35907284
NM_139215.3(TAF15):c.606-321_606-317del rs143898560
NM_139215.3(TAF15):c.673+56del rs76903662
NM_139215.3(TAF15):c.673+56dup rs76903662
NM_139215.3(TAF15):c.783+142G>C rs3760327
NM_139215.3(TAF15):c.8-17C>A rs115282214
NM_139215.3(TAF15):c.913+48dup rs4251773
NM_139215.3(TAF15):c.927T>A (p.His309Gln) rs2143826554

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