ClinVar Miner

List of variants in gene BIN1 reported as likely benign for not provided

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_139343.3(BIN1):c.85-4981C>G rs113741343 0.03437
NM_139343.3(BIN1):c.1132-91C>G rs142568045 0.02451
NM_139343.3(BIN1):c.857+134G>T rs111897541 0.02342
NM_139343.3(BIN1):c.85-5416G>A rs148981230 0.02222
NM_139343.3(BIN1):c.1462-94C>T rs115511091 0.01537
NM_139343.3(BIN1):c.1003-212G>T rs116250503 0.01509
NM_139343.3(BIN1):c.1263+310T>C rs78308373 0.01451
NM_139343.3(BIN1):c.857+1410C>G rs75761293 0.01128
NM_139343.3(BIN1):c.857+22G>A rs115112451 0.01001
NM_139343.3(BIN1):c.857+180G>A rs144499428 0.00979
NM_139343.3(BIN1):c.612+242A>G rs116527141 0.00738
NM_139343.3(BIN1):c.1003-312G>T rs143611564 0.00695
NM_139343.3(BIN1):c.520-85C>G rs142862911 0.00645
NM_139343.3(BIN1):c.1371+201C>T rs147718472 0.00567
NM_139343.3(BIN1):c.698+50G>A rs116251462 0.00508
NM_139343.3(BIN1):c.1263+259G>C rs115126471 0.00502
NM_139343.3(BIN1):c.1674+192G>A rs114740593 0.00497
NM_139343.3(BIN1):c.165+44C>T rs73953230 0.00484
NM_139343.3(BIN1):c.1461+46G>A rs139598933 0.00469
NM_139343.3(BIN1):c.1131+53C>T rs115790292 0.00460
NM_139343.3(BIN1):c.612+143_612+144del rs149861120 0.00449
NM_139343.3(BIN1):c.520-140G>A rs147622091 0.00428
NM_139343.3(BIN1):c.411+87G>A rs191287929 0.00411
NM_139343.3(BIN1):c.888C>T (p.Ser296=) rs114833236 0.00403
NM_139343.3(BIN1):c.166-52G>A rs143941695 0.00342
NC_000002.12:g.127107512G>C rs569136401 0.00335
NM_139343.3(BIN1):c.1131+301G>A rs531903369 0.00149
NM_139343.3(BIN1):c.858-1462G>A rs117721706 0.00105
NM_139343.3(BIN1):c.1611C>T (p.Asp537=) rs142523172 0.00101
NM_139343.3(BIN1):c.519+40G>A rs372195051 0.00087
NM_139343.3(BIN1):c.30G>A (p.Thr10=) rs35535012 0.00067
NM_139343.3(BIN1):c.906C>T (p.Gly302=) rs371258305 0.00031
NM_139343.3(BIN1):c.402C>T (p.Pro134=) rs144136512 0.00023
NM_139343.3(BIN1):c.1143G>A (p.Pro381=) rs372360787 0.00018
NM_139343.3(BIN1):c.1003-11C>G rs759676621 0.00014
NM_139343.3(BIN1):c.942C>T (p.His314=) rs370911793 0.00010
NM_139343.3(BIN1):c.636C>T (p.Ala212=) rs201238412 0.00009
NM_139343.3(BIN1):c.*1C>T rs770804438 0.00006
NM_139343.3(BIN1):c.822C>T (p.His274=) rs368730077 0.00006
NM_139343.3(BIN1):c.858-1472C>G rs185803812 0.00006
NM_139343.3(BIN1):c.924C>T (p.Pro308=) rs367611371 0.00005
NM_139343.3(BIN1):c.1197G>A (p.Pro399=) rs370728071 0.00003
NM_139343.3(BIN1):c.450C>T (p.Tyr150=) rs550177667 0.00003
NM_139343.3(BIN1):c.393C>T (p.Gly131=) rs1455926606 0.00002
NM_139343.3(BIN1):c.1131+10G>A rs1289102269 0.00001
NC_000002.12:g.127107528C>G rs77260225
NM_004305.4(BIN1):c.85-5345C>T rs565684463
NM_139343.3(BIN1):c.*82C>A rs111649895
NM_139343.3(BIN1):c.1017A>C (p.Pro339=)
NM_139343.3(BIN1):c.1124C>G (p.Pro375Arg) rs2104935838
NM_139343.3(BIN1):c.1227G>A (p.Thr409=)
NM_139343.3(BIN1):c.129G>A (p.Gln43=) rs1573688889
NM_139343.3(BIN1):c.1422C>T (p.Ala474=) rs1573533037
NM_139343.3(BIN1):c.1515C>T (p.Thr505=) rs375583449
NM_139343.3(BIN1):c.1573-63C>G rs7558000
NM_139343.3(BIN1):c.520-141C>T rs183752532
NM_139343.3(BIN1):c.543C>T (p.Ala181=)
NM_139343.3(BIN1):c.698+77_698+97dup rs1197231684

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