ClinVar Miner

List of variants in gene BICD2 reported as likely benign for not provided

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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_001003800.2(BICD2):c.2258+101G>A rs116139949 0.03514
NM_001003800.2(BICD2):c.2106+212C>T rs115209430 0.01259
NM_001003800.2(BICD2):c.606+111A>C rs139023495 0.01081
NM_001003800.2(BICD2):c.2259-285G>A rs115497220 0.00988
NM_001003800.2(BICD2):c.1062+120A>G rs115003966 0.00986
NM_001003800.2(BICD2):c.*136G>A rs76331256 0.00984
NM_001003800.2(BICD2):c.241-294C>T rs116144068 0.00894
NM_001003800.2(BICD2):c.269A>G (p.Lys90Arg) rs61754130 0.00437
NM_001003800.2(BICD2):c.2107-83C>T rs187669484 0.00397
NM_001003800.2(BICD2):c.241-267A>C rs188183466 0.00375
NM_001003800.2(BICD2):c.2106+86G>A rs188053727 0.00339
NM_001003800.2(BICD2):c.2445G>A (p.Pro815=) rs34451610 0.00337
NM_001003800.2(BICD2):c.1806G>A (p.Thr602=) rs138300993 0.00118
NM_001003800.2(BICD2):c.813C>T (p.Phe271=) rs150389188 0.00086
NM_001003800.2(BICD2):c.72C>G (p.Ala24=) rs545512590 0.00078
NM_001003800.2(BICD2):c.1179T>A (p.Asn393Lys) rs144427583 0.00066
NM_001003800.2(BICD2):c.2397C>T (p.Leu799=) rs151133287 0.00061
NM_001003800.2(BICD2):c.1893C>T (p.Ile631=) rs141414055 0.00040
NM_001003800.2(BICD2):c.1842A>G (p.Pro614=) rs200912578 0.00024
NM_001003800.2(BICD2):c.1250A>G (p.Asp417Gly) rs55658812 0.00014
NM_001003800.2(BICD2):c.1620C>T (p.His540=) rs375331979 0.00011
NM_001003800.2(BICD2):c.1370G>A (p.Arg457His) rs370118099 0.00008
NM_001003800.2(BICD2):c.2350A>G (p.Met784Val) rs149891938 0.00008
NM_001003800.2(BICD2):c.1749C>T (p.Pro583=) rs777813587 0.00006
NM_001003800.2(BICD2):c.1932C>T (p.Ala644=) rs201930889 0.00005
NM_001003800.2(BICD2):c.1696C>T (p.Arg566Cys) rs748022488 0.00004
NM_001003800.2(BICD2):c.1079C>T (p.Ala360Val) rs587777884 0.00003
NM_001003800.2(BICD2):c.1659G>A (p.Met553Ile) rs374912668 0.00003
NM_001003800.2(BICD2):c.165C>T (p.His55=) rs150915279 0.00003
NM_001003800.2(BICD2):c.1707C>T (p.Pro569=) rs552160043 0.00003
NM_001003800.2(BICD2):c.1725C>G (p.Pro575=) rs201343832 0.00003
NM_001003800.2(BICD2):c.2192A>G (p.Asn731Ser) rs756538071 0.00003
NM_001003800.2(BICD2):c.1534G>A (p.Val512Ile) rs748921807 0.00002
NM_001003800.2(BICD2):c.1964G>A (p.Arg655His) rs143242735 0.00002
NM_001003800.2(BICD2):c.2112C>T (p.Ala704=) rs767670894 0.00002
NM_001003800.2(BICD2):c.1276G>C (p.Glu426Gln) rs184465241 0.00001
NM_001003800.2(BICD2):c.1500C>T (p.Ala500=) rs1275858663 0.00001
NM_001003800.2(BICD2):c.1714C>T (p.Arg572Cys) rs757277531 0.00001
NM_001003800.2(BICD2):c.2258+6C>T rs566572599 0.00001
NM_001003800.2(BICD2):c.2505C>T (p.Ala835=) rs566505973 0.00001
NM_001003800.2(BICD2):c.1398G>A (p.Gln466=) rs1587669084
NM_001003800.2(BICD2):c.198G>T (p.Val66=) rs925398641
NM_001003800.2(BICD2):c.1993G>T (p.Val665Leu) rs587777885
NM_001003800.2(BICD2):c.2397C>A (p.Leu799=) rs151133287
NM_001003800.2(BICD2):c.240+222G>A rs114439546
NM_001003800.2(BICD2):c.386G>A (p.Arg129His) rs780485203

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