ClinVar Miner

List of variants in gene NEB reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 51
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HGVS dbSNP
NM_001271208.2(NEB):c.10118G>A (p.Arg3373Gln) rs568814745
NM_001271208.2(NEB):c.10181T>C (p.Ile3394Thr) rs376182104
NM_001271208.2(NEB):c.11341C>T (p.Arg3781Trp) rs533027587
NM_001271208.2(NEB):c.11461A>T (p.Met3821Leu) rs1057524782
NM_001271208.2(NEB):c.11575C>T (p.Arg3859Trp) rs562669490
NM_001271208.2(NEB):c.11621T>C (p.Leu3874Pro) rs1131691534
NM_001271208.2(NEB):c.11798T>C (p.Met3933Thr) rs772235127
NM_001271208.2(NEB):c.11828A>G (p.Asp3943Gly) rs371102558
NM_001271208.2(NEB):c.12278C>T (p.Pro4093Leu) rs749270501
NM_001271208.2(NEB):c.1258-7C>G rs371265681
NM_001271208.2(NEB):c.13411T>A (p.Tyr4471Asn) rs1057521720
NM_001271208.2(NEB):c.17048C>T (p.Ala5683Val) rs761829162
NM_001271208.2(NEB):c.17101A>G (p.Arg5701Gly) rs1332674015
NM_001271208.2(NEB):c.17203G>A (p.Ala5735Thr) rs202111641
NM_001271208.2(NEB):c.17677A>G (p.Thr5893Ala) rs762095177
NM_001271208.2(NEB):c.18862G>A (p.Val6288Ile) rs201886728
NM_001271208.2(NEB):c.1899A>T (p.Arg633Ser) rs77826191
NM_001271208.2(NEB):c.19219G>A (p.Glu6407Lys) rs144539316
NM_001271208.2(NEB):c.19406G>A (p.Arg6469Gln) rs556624010
NM_001271208.2(NEB):c.19477G>C (p.Val6493Leu) rs1233717326
NM_001271208.2(NEB):c.19543C>T (p.Arg6515Cys) rs765363585
NM_001271208.2(NEB):c.19901T>C (p.Val6634Ala) rs771989092
NM_001271208.2(NEB):c.20158-6A>G rs1553715636
NM_001271208.2(NEB):c.203G>A (p.Arg68Lys) rs1014627144
NM_001271208.2(NEB):c.20777T>C (p.Met6926Thr) rs763737123
NM_001271208.2(NEB):c.20956G>C (p.Asp6986His) rs150874422
NM_001271208.2(NEB):c.21341G>A (p.Arg7114Gln) rs372284984
NM_001271208.2(NEB):c.2200C>G (p.Gln734Glu) rs780299519
NM_001271208.2(NEB):c.2366A>G (p.Asp789Gly) rs201498216
NM_001271208.2(NEB):c.2639G>A (p.Arg880His) rs202026890
NM_001271208.2(NEB):c.3416C>T (p.Thr1139Met) rs181244403
NM_001271208.2(NEB):c.4528G>A (p.Glu1510Lys) rs370064863
NM_001271208.2(NEB):c.5153A>T (p.Gln1718Leu) rs1064796520
NM_001271208.2(NEB):c.5698_5703del (p.Tyr1900_Asn1901del) rs775531807
NM_001271208.2(NEB):c.5747T>C (p.Met1916Thr) rs142540692
NM_001271208.2(NEB):c.5828T>C (p.Leu1943Pro) rs531692437
NM_001271208.2(NEB):c.5854A>G (p.Met1952Val) rs200649387
NM_001271208.2(NEB):c.6075+3A>T rs986325764
NM_001271208.2(NEB):c.61G>A (p.Glu21Lys) rs199907781
NM_001271208.2(NEB):c.7252T>A (p.Trp2418Arg) rs780437384
NM_001271208.2(NEB):c.7312G>A (p.Ala2438Thr) rs202233025
NM_001271208.2(NEB):c.7582G>A (p.Asp2528Asn) rs369496057
NM_001271208.2(NEB):c.7696C>T (p.Arg2566Trp) rs368232288
NM_001271208.2(NEB):c.7722G>T (p.Met2574Ile) rs748066063
NM_001271208.2(NEB):c.8644G>A (p.Asp2882Asn) rs200729207
NM_001271208.2(NEB):c.8800C>T (p.Arg2934Cys) rs771598053
NM_001271208.2(NEB):c.9007C>G (p.Leu3003Val) rs1415513452
NM_001271208.2(NEB):c.9047G>A (p.Arg3016Gln) rs373587647
NM_001271208.2(NEB):c.9146T>C (p.Ile3049Thr) rs776759120
NM_001271208.2(NEB):c.9181A>T (p.Met3061Leu) rs143473183
NM_001271208.2(NEB):c.9578A>G (p.Glu3193Gly) rs369985728

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