ClinVar Miner

List of variants in gene BICD2 reported as uncertain significance for not provided

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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_001003800.2(BICD2):c.1893C>T (p.Ile631=) rs141414055 0.00040
NM_001003800.2(BICD2):c.1069C>T (p.Arg357Trp) rs202119238 0.00022
NM_001003800.2(BICD2):c.1540G>A (p.Gly514Ser) rs200091763 0.00021
NM_001003800.2(BICD2):c.2245A>G (p.Met749Val) rs145923602 0.00008
NM_001003800.2(BICD2):c.2142G>C (p.Lys714Asn) rs777986224 0.00007
NM_001003800.2(BICD2):c.1168C>A (p.Leu390Ile) rs192669216 0.00006
NM_001003800.2(BICD2):c.602A>G (p.Asn201Ser) rs201274230 0.00006
NM_001003800.2(BICD2):c.1421A>G (p.Tyr474Cys) rs1014182946 0.00004
NM_001003800.2(BICD2):c.1715G>A (p.Arg572His) rs777902159 0.00004
NM_001003800.2(BICD2):c.2331G>A (p.Thr777=) rs779170531 0.00004
NM_001003800.2(BICD2):c.640C>T (p.Arg214Cys) rs201293367 0.00004
NM_001003800.2(BICD2):c.355C>A (p.Leu119Ile) rs377156663 0.00003
NM_001003800.2(BICD2):c.638A>G (p.Lys213Arg) rs755962512 0.00003
NM_001003800.2(BICD2):c.1417C>T (p.Arg473Cys) rs142203302 0.00002
NM_001003800.2(BICD2):c.1477C>T (p.Arg493Cys) rs146113445 0.00002
NM_001003800.2(BICD2):c.1805C>T (p.Thr602Met) rs369050350 0.00002
NM_001003800.2(BICD2):c.365A>G (p.Gln122Arg) rs1477596230 0.00002
NM_001003800.2(BICD2):c.410C>T (p.Ser137Leu) rs779298360 0.00002
NM_001003800.2(BICD2):c.478C>T (p.Arg160Cys) rs754493702 0.00002
NM_001003800.2(BICD2):c.1351G>A (p.Glu451Lys) rs150965296 0.00001
NM_001003800.2(BICD2):c.1556G>T (p.Ser519Ile) rs940304129 0.00001
NM_001003800.2(BICD2):c.162G>C (p.Lys54Asn) rs779949554 0.00001
NM_001003800.2(BICD2):c.1790G>A (p.Arg597Gln) rs1412401979 0.00001
NM_001003800.2(BICD2):c.2169C>T (p.Thr723=) rs770335133 0.00001
NM_001003800.2(BICD2):c.295C>T (p.Arg99Trp) rs751756270 0.00001
NM_001003800.2(BICD2):c.1063A>T (p.Met355Leu) rs767226677
NM_001003800.2(BICD2):c.1121A>G (p.Glu374Gly) rs2131501343
NM_001003800.2(BICD2):c.1168C>T (p.Leu390Phe) rs192669216
NM_001003800.2(BICD2):c.1249G>A (p.Asp417Asn)
NM_001003800.2(BICD2):c.1294C>A (p.Pro432Thr)
NM_001003800.2(BICD2):c.1310G>C (p.Cys437Ser)
NM_001003800.2(BICD2):c.1333G>A (p.Glu445Lys) rs1057520883
NM_001003800.2(BICD2):c.1405G>C (p.Glu469Gln) rs756111549
NM_001003800.2(BICD2):c.1428T>G (p.Ala476=)
NM_001003800.2(BICD2):c.1562G>A (p.Ser521Asn) rs1853397224
NM_001003800.2(BICD2):c.1612T>C (p.Tyr538His) rs2131500475
NM_001003800.2(BICD2):c.1658T>G (p.Met553Arg)
NM_001003800.2(BICD2):c.170del (p.Leu57fs)
NM_001003800.2(BICD2):c.1762A>G (p.Lys588Glu) rs1554705436
NM_001003800.2(BICD2):c.1934T>A (p.Val645Glu) rs2131499781
NM_001003800.2(BICD2):c.2048_2059dup (p.Lys686_Arg687insLeuSerThrLys)
NM_001003800.2(BICD2):c.2066A>G (p.Gln689Arg) rs1554705339
NM_001003800.2(BICD2):c.2109G>A (p.Thr703=)
NM_001003800.2(BICD2):c.2196G>T (p.Glu732Asp)
NM_001003800.2(BICD2):c.2239C>T (p.Arg747Cys) rs1587667544
NM_001003800.2(BICD2):c.2368C>T (p.Leu790=)
NM_001003800.2(BICD2):c.2420G>A (p.Arg807Gln) rs1564057942
NM_001003800.2(BICD2):c.2422C>T (p.Arg808Cys) rs143189118
NM_001003800.2(BICD2):c.301G>A (p.Glu101Lys) rs1554706635
NM_001003800.2(BICD2):c.527G>A (p.Arg176His) rs1207286970
NM_001003800.2(BICD2):c.547G>T (p.Glu183Ter)
NM_001003800.2(BICD2):c.613_633del (p.Phe205_Glu211del) rs1564061350
NM_001003800.2(BICD2):c.754G>A (p.Glu252Lys) rs776953074
NM_001003800.2(BICD2):c.856A>G (p.Ser286Gly)
NM_001003800.2(BICD2):c.877AAC[1] (p.Asn294del)

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