ClinVar Miner

List of variants in gene combination NEB, RIF1 reported as uncertain significance by GeneDx

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Total variants: 21
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HGVS dbSNP
NM_001271208.1(NEB):c.21442A>G (p.Met7148Val) rs750039342
NM_001271208.1(NEB):c.21522+3A>G rs148950085
NM_001271208.1(NEB):c.21769T>A (p.Ser7257Thr) rs191722579
NM_001271208.1(NEB):c.22109C>T (p.Thr7370Met) rs767584361
NM_001271208.1(NEB):c.22127C>T (p.Ala7376Val) rs550296441
NM_001271208.1(NEB):c.22373G>A (p.Ser7458Asn) rs759974940
NM_001271208.1(NEB):c.22501C>T (p.Arg7501Cys) rs768826001
NM_001271208.1(NEB):c.22777A>T (p.Asn7593Tyr) rs771643485
NM_001271208.1(NEB):c.22937G>A (p.Arg7646Gln) rs766072117
NM_001271208.1(NEB):c.23383A>G (p.Asn7795Asp) rs201189784
NM_001271208.1(NEB):c.23582A>G (p.Asn7861Ser) rs143602832
NM_001271208.1(NEB):c.23605G>T (p.Val7869Phe) rs1553601424
NM_001271208.1(NEB):c.23847+5T>C rs1553594314
NM_001271208.1(NEB):c.24089T>C (p.Met8030Thr) rs1064796521
NM_001271208.1(NEB):c.24313-7C>A rs113048349
NM_001271208.1(NEB):c.24443T>C (p.Leu8148Pro) rs1057524553
NM_001271208.1(NEB):c.24607_24609dupAAT (p.Asn8203_Val8204insAsn) rs1057518617
NM_001271208.1(NEB):c.25472C>T (p.Thr8491Met) rs78592085
NM_004543.4(NEB):c.17747A>G (p.Asp5916Gly) rs776739582
NM_004543.4(NEB):c.18046G>C (p.Glu6016Gln) rs766321668
NM_004543.4(NEB):c.19597C>T (p.Arg6533Trp) rs373551215

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