ClinVar Miner

List of variants in gene BCORL1 reported as likely benign for not provided

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Gene type:
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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_001379451.1(BCORL1):c.516T>C (p.Asn172=) rs36043572 0.00612
NM_001379451.1(BCORL1):c.783G>A (p.Ala261=) rs61752973 0.00428
NM_001379451.1(BCORL1):c.882G>A (p.Pro294=) rs200510623 0.00070
NM_001379451.1(BCORL1):c.280G>A (p.Asp94Asn) rs139887979 0.00068
NM_001379451.1(BCORL1):c.2648G>A (p.Gly883Glu) rs138477961 0.00050
NM_001379451.1(BCORL1):c.3555G>A (p.Pro1185=) rs61754128 0.00027
NM_001379451.1(BCORL1):c.2669G>A (p.Arg890Gln) rs201843717 0.00022
NM_001379451.1(BCORL1):c.62G>A (p.Arg21His) rs778701486 0.00017
NM_001379451.1(BCORL1):c.3521A>G (p.Asn1174Ser) rs147703991 0.00014
NM_001379451.1(BCORL1):c.2424G>A (p.Thr808=) rs138691600 0.00013
NM_001379451.1(BCORL1):c.472G>A (p.Gly158Arg) rs376946512 0.00007
NM_001379451.1(BCORL1):c.1059G>A (p.Pro353=) rs372535982 0.00003
NM_001379451.1(BCORL1):c.2410T>C (p.Leu804=) rs150199677 0.00002
NM_001379451.1(BCORL1):c.837C>T (p.Ala279=) rs770800501 0.00002
NM_001379451.1(BCORL1):c.2820C>T (p.Ser940=) rs748965394 0.00001
NM_001379451.1(BCORL1):c.1065G>A (p.Val355=)
NM_001379451.1(BCORL1):c.1092C>T (p.Ser364=)
NM_001379451.1(BCORL1):c.1130C>A (p.Ala377Asp) rs768067473
NM_001379451.1(BCORL1):c.1596C>G (p.Ser532=)
NM_001379451.1(BCORL1):c.1623C>G (p.Pro541=)
NM_001379451.1(BCORL1):c.1791C>G (p.Thr597=)
NM_001379451.1(BCORL1):c.1794C>T (p.Phe598=)
NM_001379451.1(BCORL1):c.1902A>G (p.Pro634=) rs1603112868
NM_001379451.1(BCORL1):c.2016C>T (p.Ala672=)
NM_001379451.1(BCORL1):c.2075A>G (p.Glu692Gly)
NM_001379451.1(BCORL1):c.214C>T (p.Arg72Trp)
NM_001379451.1(BCORL1):c.2277T>A (p.Pro759=)
NM_001379451.1(BCORL1):c.2593G>A (p.Val865Ile)
NM_001379451.1(BCORL1):c.2635G>A (p.Glu879Lys)
NM_001379451.1(BCORL1):c.2664A>G (p.Gln888=)
NM_001379451.1(BCORL1):c.2912C>G (p.Ala971Gly)
NM_001379451.1(BCORL1):c.312C>T (p.Asn104=)
NM_001379451.1(BCORL1):c.3269G>C (p.Arg1090Pro)
NM_001379451.1(BCORL1):c.3415G>A (p.Val1139Met)
NM_001379451.1(BCORL1):c.3570C>T (p.Ser1190=)
NM_001379451.1(BCORL1):c.3609T>A (p.Gly1203=)
NM_001379451.1(BCORL1):c.387C>T (p.Ser129=)
NM_001379451.1(BCORL1):c.3882C>T (p.His1294=)
NM_001379451.1(BCORL1):c.4068A>G (p.Lys1356=)
NM_001379451.1(BCORL1):c.4146C>A (p.Asn1382Lys)
NM_001379451.1(BCORL1):c.4188A>C (p.Pro1396=)
NM_001379451.1(BCORL1):c.429A>T (p.Pro143=)
NM_001379451.1(BCORL1):c.4306-4C>T
NM_001379451.1(BCORL1):c.4360G>A (p.Val1454Met)
NM_001379451.1(BCORL1):c.4381A>G (p.Thr1461Ala)
NM_001379451.1(BCORL1):c.4413G>A (p.Glu1471=)
NM_001379451.1(BCORL1):c.4656C>T (p.His1552=)
NM_001379451.1(BCORL1):c.5007T>C (p.Asp1669=)
NM_001379451.1(BCORL1):c.5030A>G (p.Lys1677Arg)
NM_001379451.1(BCORL1):c.5184C>T (p.Ala1728=)
NM_001379451.1(BCORL1):c.624C>T (p.Pro208=)
NM_001379451.1(BCORL1):c.784C>G (p.Pro262Ala)
NM_001379451.1(BCORL1):c.912G>A (p.Pro304=)
NM_001379451.1(BCORL1):c.993T>A (p.Ala331=)

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