ClinVar Miner

List of variants in gene NIPA1 reported as benign

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Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_144599.5(NIPA1):c.*1981A>G rs6606822 0.99970
NM_144599.5(NIPA1):c.*1974C>A rs6606823 0.93707
NM_144599.5(NIPA1):c.317+190C>G rs7168401 0.93290
NM_144599.5(NIPA1):c.*2058_*2059insTT rs3057642 0.67258
NM_144599.5(NIPA1):c.441A>G (p.Thr147=) rs11263683 0.65973
NM_144599.5(NIPA1):c.*972C>T rs8025849 0.65255
NM_144599.5(NIPA1):c.*4933C>T rs7181789 0.57025
NM_144599.5(NIPA1):c.*1127C>G rs1059774 0.32452
NM_144599.5(NIPA1):c.*1927A>G rs17807140 0.28781
NM_144599.5(NIPA1):c.479-29C>T rs12592629 0.28001
NM_144599.5(NIPA1):c.479-239C>T rs61656257 0.27635
NM_144599.4(NIPA1):c.-359C>G rs62001112 0.25272
NM_144599.5(NIPA1):c.*287T>C rs3812924 0.22372
NM_144599.5(NIPA1):c.*2425A>G rs12902722 0.10277
NM_144599.5(NIPA1):c.*1563C>T rs72698098 0.09246
NM_144599.5(NIPA1):c.317+216T>C rs60823980 0.06496
NM_144599.5(NIPA1):c.227-93C>T rs74003090 0.06365
NM_144599.5(NIPA1):c.*3702C>T rs3812923 0.03905
NM_144599.5(NIPA1):c.226+163C>T rs17137329 0.02935
NM_144599.5(NIPA1):c.*3278C>G rs57615013 0.02793
NM_144599.5(NIPA1):c.*2649A>G rs8027756 0.02539
NM_144599.5(NIPA1):c.478+154C>T rs59940862 0.02515
NM_144599.5(NIPA1):c.*5331T>G rs73412681 0.02493
NM_144599.5(NIPA1):c.*2469A>G rs73412688 0.02406
NM_144599.5(NIPA1):c.*5299G>C rs73412682 0.02310
NM_144599.5(NIPA1):c.*4734G>C rs73412685 0.02303
NM_144599.5(NIPA1):c.318-68A>G rs77146068 0.01863
NM_144599.5(NIPA1):c.*1405G>C rs7181585 0.01455
NM_144599.5(NIPA1):c.*4363C>T rs139459875 0.00724
NM_144599.5(NIPA1):c.*3910G>A rs74767096 0.00528
NM_144599.5(NIPA1):c.*3393A>T rs147611065 0.00427
NM_144599.5(NIPA1):c.*1012A>G rs186626641 0.00366
NM_144599.5(NIPA1):c.*5237G>C rs74003089 0.00338
NM_144599.5(NIPA1):c.*5044G>C rs191543264 0.00270
NM_144599.5(NIPA1):c.*4218G>A rs182099304 0.00240
NM_144599.5(NIPA1):c.*3480C>T rs112696483 0.00216
NM_144599.5(NIPA1):c.*5071C>T rs141920126 0.00185
NM_144599.5(NIPA1):c.*4964G>A rs146129067 0.00179
NM_144599.5(NIPA1):c.*2780G>T rs183353690 0.00178
NM_144599.5(NIPA1):c.*3590A>G rs145202306 0.00130
NM_144599.5(NIPA1):c.*5185C>T rs569739849 0.00127
NM_144599.5(NIPA1):c.*4885T>C rs555159081 0.00106
NM_144599.5(NIPA1):c.906C>T (p.Ser302=) rs147070285 0.00080
NM_144599.5(NIPA1):c.*1724C>G rs61523596 0.00069
NM_144599.5(NIPA1):c.*4774G>A rs541776619 0.00066
NM_144599.5(NIPA1):c.*4716G>A rs540912938 0.00054
NM_144599.5(NIPA1):c.312G>A (p.Pro104=) rs139372534 0.00051
NM_144599.5(NIPA1):c.*11G>C rs188393827 0.00036
NM_144599.5(NIPA1):c.*3400C>T rs577663387 0.00029
NM_144599.5(NIPA1):c.*1395C>T rs537516417 0.00021
NM_144599.5(NIPA1):c.801G>T (p.Val267=) rs185222838 0.00020
NM_144599.5(NIPA1):c.*3872T>G rs528309949 0.00015
NM_144599.5(NIPA1):c.*4792G>T rs139161065 0.00015
NM_144599.5(NIPA1):c.*1146T>C rs181621508 0.00006
NM_144599.5(NIPA1):c.537C>T (p.Ile179=) rs547634456 0.00006
NM_144599.5(NIPA1):c.*4510T>C rs528249723 0.00004
NC_000015.9:g.(?_23086214)_(23086411_?)dup
NM_001142275.1(NIPA1):c.-48+200del rs142739374
NM_144599.5(NIPA1):c.*1846dup rs113532349
NM_144599.5(NIPA1):c.*2515G>C rs6606820
NM_144599.5(NIPA1):c.*435_*436del rs10611411
NM_144599.5(NIPA1):c.478+232_478+237del rs145447453
NM_144599.5(NIPA1):c.508C>G (p.Leu170Val) rs1895592461

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