ClinVar Miner

List of variants in gene NEB reported as benign by PreventionGenetics

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Gene type:
ClinVar version:
Total variants: 111
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HGVS dbSNP
NM_001271208.1(NEB):c.10338T>C (p.Asn3446=) rs147569843
NM_001271208.1(NEB):c.10344C>T (p.Asn3448=) rs145052299
NM_001271208.1(NEB):c.10347+6C>T rs141088433
NM_001271208.1(NEB):c.10452+9A>G rs117270796
NM_001271208.1(NEB):c.10463G>A (p.Arg3488His) rs371605774
NM_001271208.1(NEB):c.10872+27A>C rs10186656
NM_001271208.1(NEB):c.11004G>A (p.Thr3668=) rs117018177
NM_001271208.1(NEB):c.1152+49A>G rs113401628
NM_001271208.1(NEB):c.12018+29G>A rs11902616
NM_001271208.1(NEB):c.12667G>A (p.Ala4223Thr) rs12998234
NM_001271208.1(NEB):c.13105C>T (p.Leu4369=) rs147579763
NM_001271208.1(NEB):c.13276G>A (p.Asp4426Asn) rs876657540
NM_001271208.1(NEB):c.13353C>T (p.Ala4451=) rs774726264
NM_001271208.1(NEB):c.13368+11A>G rs112260335
NM_001271208.1(NEB):c.13476C>T (p.Asp4492=) rs876657541
NM_001271208.1(NEB):c.13534G>A (p.Ala4512Thr) rs886038435
NM_001271208.1(NEB):c.13626C>G (p.Ala4542=) rs201225445
NM_001271208.1(NEB):c.13628A>C (p.Lys4543Thr) rs200125713
NM_001271208.1(NEB):c.13753A>G (p.Ile4585Val) rs886038440
NM_001271208.1(NEB):c.1413C>T (p.Phe471=) rs112958786
NM_001271208.1(NEB):c.14734A>G (p.Asn4912Asp) rs10909569
NM_001271208.1(NEB):c.14914T>A (p.Ser4972Thr) rs776187492
NM_001271208.1(NEB):c.14934+16_14934+17insG rs11436831
NM_001271208.1(NEB):c.15086A>C (p.Lys5029Thr) rs200053313
NM_001271208.1(NEB):c.15179A>G (p.His5060Arg) rs886038444
NM_001271208.1(NEB):c.16021T>C (p.Leu5341=) rs796103760
NM_001271208.1(NEB):c.16269C>T (p.Ala5423=) rs542916866
NM_001271208.1(NEB):c.16284+11A>G rs367881797
NM_001271208.1(NEB):c.16449C>T (p.Ser5483=) rs546992311
NM_001271208.1(NEB):c.16450G>A (p.Ala5484Thr) rs536508687
NM_001271208.1(NEB):c.16542C>G (p.Ala5514=) rs200602229
NM_001271208.1(NEB):c.16544A>C (p.Lys5515Thr) rs62174690
NM_001271208.1(NEB):c.16637G>A (p.Arg5546His) rs201111610
NM_001271208.1(NEB):c.16704+12G>C rs62174689
NM_001271208.1(NEB):c.16705-18C>T rs61254943
NM_001271208.1(NEB):c.1674+30T>G rs6433569
NM_001271208.1(NEB):c.17049G>T (p.Ala5683=) rs140688592
NM_001271208.1(NEB):c.17887G>A (p.Val5963Ile) rs138217960
NM_001271208.1(NEB):c.1856A>G (p.Lys619Arg) rs147305883
NM_001271208.1(NEB):c.18580-32C>T rs62174683
NM_001271208.1(NEB):c.18783G>A (p.Gln6261=) rs148095660
NM_001271208.1(NEB):c.18861C>T (p.Arg6287=) rs146294986
NM_001271208.1(NEB):c.19101+41C>T rs4364020
NM_001271208.1(NEB):c.19314+42C>T rs2288206
NM_001271208.1(NEB):c.195G>A (p.Pro65=) rs79524813
NM_001271208.1(NEB):c.20158-42G>A rs2288201
NM_001271208.1(NEB):c.20998-44A>C rs3732310
NM_001271208.1(NEB):c.2318A>G (p.Tyr773Cys) rs77151072
NM_001271208.1(NEB):c.2832C>T (p.Ser944=) rs114076205
NM_001271208.1(NEB):c.3348C>T (p.Asn1116=) rs149162847
NM_001271208.1(NEB):c.3879+20G>T rs12618063
NM_001271208.1(NEB):c.4272G>C (p.Thr1424=) rs35654397
NM_001271208.1(NEB):c.5031+48A>G rs4664496
NM_001271208.1(NEB):c.5763+35T>C rs12620077
NM_001271208.1(NEB):c.6069G>A (p.Met2023Ile) rs184262608
NM_001271208.1(NEB):c.612+15C>T rs112288851
NM_001271208.1(NEB):c.6184-14T>A rs10173335
NM_001271208.1(NEB):c.7514C>A (p.Ala2505Glu) rs35292878
NM_001271208.1(NEB):c.822+25_822+27dupGCC rs397718862
NM_001271208.1(NEB):c.8646C>T (p.Asp2882=) rs61730773
NM_001271208.1(NEB):c.9052G>A (p.Asp3018Asn) rs192098032
NM_001271208.1(NEB):c.9072G>A (p.Ala3024=) rs369897667
NM_001271208.1(NEB):c.9124T>C (p.Cys3042Arg) rs6710212
NM_001271208.1(NEB):c.9363T>C (p.Pro3121=) rs6709886
NM_001271208.1(NEB):c.9467T>A (p.Ile3156Asn) rs145770770
NM_004543.4(NEB):c.10080G>C (p.Trp3360Cys) rs10172023
NM_004543.4(NEB):c.11000A>G (p.Asp3667Gly) rs35740585
NM_004543.4(NEB):c.11659T>A (p.Ser3887Thr) rs35227368
NM_004543.4(NEB):c.11808A>G (p.Pro3936=) rs33988153
NM_004543.4(NEB):c.12C>T (p.Asp4=) rs117178114
NM_004543.4(NEB):c.13191T>C (p.Tyr4397=) rs2288211
NM_004543.4(NEB):c.13202G>C (p.Arg4401Thr) rs2288210
NM_004543.4(NEB):c.13452G>A (p.Lys4484=) rs145252235
NM_004543.4(NEB):c.13590G>C (p.Ala4530=) rs141338915
NM_004543.4(NEB):c.13953G>T (p.Thr4651=) rs115631125
NM_004543.4(NEB):c.13999-6C>T rs145127681
NM_004543.4(NEB):c.14629-6C>T rs11894996
NM_004543.4(NEB):c.14975C>T (p.Thr4992Ile) rs35707762
NM_004543.4(NEB):c.15089A>T (p.Asp5030Val) rs2288200
NM_004543.4(NEB):c.15495C>G (p.Gly5165=) rs16830192
NM_004543.4(NEB):c.15663C>T (p.Asp5221=) rs34555492
NM_004543.4(NEB):c.15941C>G (p.Ser5314Cys) rs62167164
NM_004543.4(NEB):c.1675-9T>G rs75118047
NM_004543.4(NEB):c.2944-9G>A rs13427102
NM_004543.4(NEB):c.3081A>T (p.Lys1027Asn) rs6735208
NM_004543.4(NEB):c.3147+5G>A rs74859201
NM_004543.4(NEB):c.3191A>G (p.Tyr1064Cys) rs187343008
NM_004543.4(NEB):c.3412A>G (p.Asn1138Asp) rs117048449
NM_004543.4(NEB):c.4407G>C (p.Glu1469Asp) rs34800215
NM_004543.4(NEB):c.4435G>A (p.Val1479Ile) rs34577613
NM_004543.4(NEB):c.4471G>A (p.Val1491Met) rs7426114
NM_004543.4(NEB):c.5102T>C (p.Val1701Ala) rs117271684
NM_004543.4(NEB):c.5370G>A (p.Glu1790=) rs10170273
NM_004543.4(NEB):c.5567G>A (p.Arg1856Gln) rs141930814
NM_004543.4(NEB):c.571G>C (p.Glu191Gln) rs35686968
NM_004543.4(NEB):c.5772C>T (p.Tyr1924=) rs77547727
NM_004543.4(NEB):c.5905T>C (p.Tyr1969His) rs34532796
NM_004543.4(NEB):c.5971C>T (p.His1991Tyr) rs75807392
NM_004543.4(NEB):c.612+8T>C rs113095802
NM_004543.4(NEB):c.6159G>A (p.Lys2053=) rs140186806
NM_004543.4(NEB):c.6717T>G (p.Ile2239Met) rs78733601
NM_004543.4(NEB):c.6807+6T>G rs10930723
NM_004543.4(NEB):c.7310G>A (p.Arg2437Gln) rs61730780
NM_004543.4(NEB):c.771T>C (p.Ala257=) rs4611637
NM_004543.4(NEB):c.7839G>C (p.Lys2613Asn) rs13013209
NM_004543.4(NEB):c.8189A>G (p.Asp2730Gly) rs76767949
NM_004543.4(NEB):c.8318G>A (p.Arg2773Gln) rs35974308
NM_004543.4(NEB):c.8466C>T (p.His2822=) rs61730771
NM_004543.4(NEB):c.8734T>C (p.Ser2912Pro) rs6713162
NM_004543.4(NEB):c.9136G>A (p.Gly3046Ser) rs75639119
NM_004543.4(NEB):c.9978G>A (p.Lys3326=) rs6717213

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