ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP
NM_000057.4(BLM):c.1011A>T (p.Thr337=) rs773511833
NM_000057.4(BLM):c.1188T>C (p.Cys396=) rs756454608
NM_000057.4(BLM):c.1209G>A (p.Gln403=) rs1555419741
NM_000057.4(BLM):c.1221-6C>T rs1555419778
NM_000057.4(BLM):c.1362T>C (p.Asn454=) rs1156488243
NM_000057.4(BLM):c.1419C>G (p.Thr473=) rs200051680
NM_000057.4(BLM):c.1917G>A (p.Leu639=) rs771059822
NM_000057.4(BLM):c.2103C>T (p.Leu701=) rs1596234139
NM_000057.4(BLM):c.2119C>T (p.Pro707Ser) rs146077918
NM_000057.4(BLM):c.2169A>G (p.Gln723=) rs781635047
NM_000057.4(BLM):c.2202T>C (p.Ala734=) rs1596235728
NM_000057.4(BLM):c.2280A>C (p.Ile760=) rs1596236007
NM_000057.4(BLM):c.2308-6G>A rs1219227761
NM_000057.4(BLM):c.234C>T (p.Pro78=) rs970793829
NM_000057.4(BLM):c.2433C>T (p.Tyr811=) rs377542595
NM_000057.4(BLM):c.2475G>C (p.Pro825=) rs147587050
NM_000057.4(BLM):c.249G>A (p.Gln83=) rs1430623511
NM_000057.4(BLM):c.2555+7_2555+8inv
NM_000057.4(BLM):c.2598A>G (p.Val866=) rs574053990
NM_000057.4(BLM):c.2652G>A (p.Lys884=) rs1596250475
NM_000057.4(BLM):c.2655C>T (p.His885=) rs1404506326
NM_000057.4(BLM):c.2662+8C>G rs1330037075
NM_000057.4(BLM):c.3020-7C>G rs1596259789
NM_000057.4(BLM):c.3042T>C (p.His1014=) rs1060503986
NM_000057.4(BLM):c.3135T>C (p.Phe1045=) rs1596260013
NM_000057.4(BLM):c.3141A>G (p.Glu1047=) rs1596260028
NM_000057.4(BLM):c.322T>C (p.Leu108=) rs1596218180
NM_000057.4(BLM):c.3345C>T (p.Val1115=) rs773893026
NM_000057.4(BLM):c.3359-9T>C rs1060503988
NM_000057.4(BLM):c.3426C>G (p.Ala1142=) rs147148171
NM_000057.4(BLM):c.3468T>C (p.Asp1156=) rs1325465971
NM_000057.4(BLM):c.348G>A (p.Lys116=) rs749535664
NM_000057.4(BLM):c.3513G>A (p.Val1171=) rs780615126
NM_000057.4(BLM):c.3546T>C (p.Asn1182=) rs1596267753
NM_000057.4(BLM):c.3666T>A (p.Leu1222=) rs1301144106
NM_000057.4(BLM):c.3744G>A (p.Lys1248=) rs1596268347
NM_000057.4(BLM):c.3751+10C>G rs199685140
NM_000057.4(BLM):c.3759A>G (p.Leu1253=) rs1596271761
NM_000057.4(BLM):c.3840A>G (p.Ser1280=) rs759221501
NM_000057.4(BLM):c.3849G>A (p.Gln1283=) rs140524886
NM_000057.4(BLM):c.3861A>G (p.Glu1287=) rs977539638
NM_000057.4(BLM):c.3867A>G (p.Thr1289=) rs759000443
NM_000057.4(BLM):c.3876T>C (p.Ala1292=) rs1596273405
NM_000057.4(BLM):c.3894G>C (p.Gly1298=) rs1596273453
NM_000057.4(BLM):c.3936T>C (p.Ala1312=) rs1034211979
NM_000057.4(BLM):c.393C>T (p.Ser131=) rs1596218349
NM_000057.4(BLM):c.410A>G (p.Lys137Arg) rs28384988
NM_000057.4(BLM):c.4122C>T (p.Ser1374=) rs145277875
NM_000057.4(BLM):c.4164G>T (p.Ala1388=) rs1429829646
NM_000057.4(BLM):c.4179T>C (p.Asn1393=) rs1596276561
NM_000057.4(BLM):c.4200T>C (p.Ala1400=) rs1596276585
NM_000057.4(BLM):c.4209G>A (p.Lys1403=) rs1254277623
NM_000057.4(BLM):c.4215A>T (p.Ile1405=) rs1596276635
NM_000057.4(BLM):c.456T>C (p.Asn152=) rs1316621251
NM_000057.4(BLM):c.540A>T (p.Val180=) rs763776756
NM_000057.4(BLM):c.558A>G (p.Ser186=) rs982183816
NM_000057.4(BLM):c.564G>A (p.Lys188=) rs1596218841
NM_000057.4(BLM):c.648G>A (p.Glu216=) rs1208450024
NM_000057.4(BLM):c.789A>G (p.Glu263=) rs1596219365
NM_000057.4(BLM):c.800-4G>A rs1338362749
NM_000057.4(BLM):c.800-5T>C rs1596220949
NM_000057.4(BLM):c.81T>C (p.Leu27=) rs1596215726
NM_000057.4(BLM):c.822T>C (p.Asn274=) rs1596221010
NM_000057.4(BLM):c.888T>C (p.Tyr296=) rs139277089
NM_000057.4(BLM):c.906A>G (p.Pro302=) rs1596221231
NM_000057.4(BLM):c.909T>C (p.Pro303=) rs767770187

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