ClinVar Miner

List of variants in gene NME8 reported as benign by Preventiongenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_016616.5(NME8):c.271-49G>A rs2249451 0.92264
NM_016616.5(NME8):c.622T>C (p.Cys208Arg) rs10250905 0.77615
NM_016616.5(NME8):c.455-46C>T rs3816418 0.77506
NM_016616.5(NME8):c.1544+22G>A rs10261071 0.63994
NM_016616.5(NME8):c.1247+25A>G rs2242027 0.47134
NM_016616.5(NME8):c.1140-10T>G rs1530822 0.45910
NM_016616.5(NME8):c.177C>T (p.Asp59=) rs2598044 0.28287
NM_016616.5(NME8):c.91+44G>A rs2722371 0.28279
NM_016616.5(NME8):c.128G>A (p.Arg43Lys) rs2722372 0.28270
NM_016616.5(NME8):c.1478T>C (p.Ile493Thr) rs56128139 0.25213
NM_016616.5(NME8):c.1479A>T (p.Ile493=) rs41276027 0.25198
NM_016616.5(NME8):c.1603T>C (p.Leu535=) rs3213975 0.22683
NM_016616.5(NME8):c.840A>G (p.Arg280=) rs62001868 0.13654
NM_016616.5(NME8):c.219G>A (p.Val73=) rs3213976 0.08754
NM_016616.5(NME8):c.818+27T>C rs116545712 0.04206
NM_016616.5(NME8):c.1013T>C (p.Ile338Thr) rs62001870 0.03629
NM_016616.5(NME8):c.1247+34C>T rs75991941 0.01634
NM_016616.5(NME8):c.994+19A>G rs73340816 0.00665
NM_016616.5(NME8):c.271-14C>T rs75531720 0.00526
NM_016616.5(NME8):c.739G>A (p.Glu247Lys) rs139516225 0.00383
NM_016616.5(NME8):c.1007G>A (p.Arg336His) rs62001869
NM_016616.5(NME8):c.1478_1479delinsCT (p.Ile493Thr) rs386712272

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.