ClinVar Miner

List of variants in gene BLK reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_001715.3(BLK):c.176-104G>A rs6994605 0.90656
NM_001715.3(BLK):c.843T>C (p.Phe281=) rs2306234 0.81190
NC_000008.11:g.11564661A>G rs7840433 0.59878
NM_001715.3(BLK):c.1029+25A>G rs4841557 0.58734
NM_001715.3(BLK):c.1029+247T>A rs7007439 0.58270
NM_001715.3(BLK):c.1029+50C>T rs4841558 0.58188
NM_001715.3(BLK):c.-1-105C>G rs12386974 0.55690
NM_001715.3(BLK):c.330T>C (p.Ser110=) rs3816668 0.49161
NM_001715.3(BLK):c.*176C>T rs1042689 0.42891
NM_001715.3(BLK):c.1313-54C>A rs10097005 0.42867
NM_001715.3(BLK):c.176-292G>A rs11779639 0.42758
NM_001715.3(BLK):c.-1-53G>A rs2245250 0.41844
NM_001715.3(BLK):c.1181-193T>C rs7834638 0.41756
NM_001715.3(BLK):c.1313-28C>T rs10097015 0.41687
NM_001715.3(BLK):c.123+88G>T rs2245232 0.41611
NM_001715.3(BLK):c.123+260G>A rs11780851 0.40706
NM_001715.3(BLK):c.1030-38C>T rs4841561 0.38972
NM_001715.3(BLK):c.*428G>A rs1042701 0.34826
NM_001715.3(BLK):c.1181-267G>A rs13262953 0.34426
NM_001715.3(BLK):c.270-176G>A rs6999912 0.34292
NC_000008.11:g.11564621T>C rs7843987 0.32115
NM_001715.3(BLK):c.952+95del rs34744472 0.30892
NM_001715.3(BLK):c.176-205C>T rs11786737 0.23468
NM_001715.3(BLK):c.1313-91T>C rs13248757 0.22253
NM_001715.3(BLK):c.176-167T>G rs73195285 0.11756
NM_001715.3(BLK):c.773-274C>T rs62490880 0.10871
NM_001715.3(BLK):c.772+199T>C rs73195298 0.10500
NM_001715.3(BLK):c.1030-45G>A rs62490888 0.10477
NM_001715.3(BLK):c.1313-158C>T rs62490890 0.10474
NM_001715.3(BLK):c.270-291C>A rs28625526 0.09297
NC_000008.11:g.11564818T>C rs78453383 0.07469
NM_001715.3(BLK):c.1030-133T>C rs112254800 0.06403
NC_000008.11:g.11564671C>T rs73663168 0.05169
NM_001715.3(BLK):c.*92G>C rs14053 0.04621
NM_001715.3(BLK):c.-1-83G>A rs80167929 0.02963
NM_001715.3(BLK):c.269+218C>A rs78789099 0.02492
NM_001715.3(BLK):c.772+140C>T rs2254959 0.02466
NM_001715.3(BLK):c.123+255G>A rs60536897 0.02268
NM_001715.3(BLK):c.258G>A (p.Gln86=) rs56185487 0.02041
NM_001715.3(BLK):c.124-193G>A rs7815435 0.01874
NM_001715.3(BLK):c.1312+311C>A rs73663167 0.01860
NM_001715.3(BLK):c.473-188A>C rs112153719 0.01551
NM_001715.3(BLK):c.211G>A (p.Ala71Thr) rs55758736 0.01485
NM_001715.3(BLK):c.177C>G (p.Asp59Glu) rs146083915 0.00891
NM_001715.3(BLK):c.102C>T (p.Asp34=) rs75383960 0.00743
NM_001715.3(BLK):c.335T>C (p.Phe112Ser) rs115068920 0.00517
NM_001715.3(BLK):c.753A>G (p.Gln251=) rs76563369 0.00416
NM_001715.3(BLK):c.187G>A (p.Val63Met) rs138972988 0.00302
NM_001715.3(BLK):c.116C>T (p.Pro39Leu) rs142352008 0.00222
NM_001715.3(BLK):c.81G>A (p.Lys27=) rs149279535 0.00205
NM_001715.3(BLK):c.711C>T (p.Pro237=) rs143699141 0.00174
NM_001715.3(BLK):c.974A>C (p.Lys325Thr) rs77401687 0.00117
NM_001715.3(BLK):c.1338C>G (p.Arg446=) rs377160616 0.00073
NM_001715.3(BLK):c.879C>T (p.His293=) rs142623841 0.00034
NM_001715.3(BLK):c.1349G>A (p.Arg450His) rs202162624 0.00022
NM_001715.3(BLK):c.672C>T (p.Ala224=) rs201252364 0.00004
NM_001715.3(BLK):c.-1-254C>A rs74961098
NM_001715.3(BLK):c.-1-278T>G rs2245260
NM_001715.3(BLK):c.1029+265C>T rs6983727
NM_001715.3(BLK):c.1180+64G>C rs73545881
NM_001715.3(BLK):c.1227C>T (p.Phe409=)
NM_001715.3(BLK):c.1312+25C>G rs73545895
NM_001715.3(BLK):c.176-200C>A rs2306232
NM_001715.3(BLK):c.269+13G>C rs144839649
NM_001715.3(BLK):c.270-125G>A rs76578315
NM_001715.3(BLK):c.368+184T>C rs4841553
NM_001715.3(BLK):c.368+269T>C rs3808499
NM_001715.3(BLK):c.39G>A (p.Lys13=) rs142129056
NM_001715.3(BLK):c.772+17G>A
NM_001715.3(BLK):c.772+341C>G
NM_001715.3(BLK):c.773-154G>C rs11250147
NM_001715.3(BLK):c.952+46C>A
NM_001715.3(BLK):c.953-287C>G rs7814414

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