ClinVar Miner

List of variants in gene combination NEB, RIF1 reported as benign by PreventionGenetics

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Gene type:
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Total variants: 23
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HGVS dbSNP
NM_001271208.1(NEB):c.21487T>C (p.Leu7163=) rs114218081
NM_001271208.1(NEB):c.21523-6delA rs56026241
NM_001271208.1(NEB):c.21945+13A>C rs75515097
NM_001271208.1(NEB):c.22266+18G>C rs6721666
NM_001271208.1(NEB):c.22905+32C>T rs16830136
NM_001271208.1(NEB):c.23009G>A (p.Gly7670Glu) rs3732309
NM_001271208.1(NEB):c.23346+42T>C rs16830128
NM_001271208.1(NEB):c.23347-50_23347-47dupTGTT rs142314464
NM_001271208.1(NEB):c.23704A>C (p.Lys7902Gln) rs118191309
NM_001271208.1(NEB):c.24871-18C>T rs2288195
NM_001271208.1(NEB):c.24979-47A>T rs2288193
NM_001271208.1(NEB):c.25255+12G>A rs4414676
NM_001271208.1(NEB):c.25510-17dupT rs148839798
NM_001271208.1(NEB):c.25510-34T>C rs16830090
NM_001271208.1(NEB):c.25647C>T (p.Thr8549=) rs3821324
NM_004543.4(NEB):c.16416C>T (p.Ser5472=) rs16830170
NM_004543.4(NEB):c.16443C>T (p.Asn5481=) rs149510427
NM_004543.4(NEB):c.16482A>G (p.Thr5494=) rs4664475
NM_004543.4(NEB):c.16753G>A (p.Asp5585Asn) rs35625617
NM_004543.4(NEB):c.16860A>G (p.Lys5620=) rs61730765
NM_004543.4(NEB):c.18865G>C (p.Ala6289Pro) rs7575451
NM_004543.4(NEB):c.19636A>G (p.Ile6546Val) rs1061305
NM_004543.4(NEB):c.19827T>G (p.Ser6609=) rs13031275

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