ClinVar Miner

List of variants in gene SKIC2 reported as benign for not provided

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Gene type:
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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_006929.5(SKIC2):c.3201T>C (p.Tyr1067=) rs410851 0.79487
NM_006929.5(SKIC2):c.640A>C (p.Met214Leu) rs437179 0.77931
NM_006929.5(SKIC2):c.545-19T>C rs419788 0.77929
NM_006929.5(SKIC2):c.126+165A>G rs440454 0.77926
NM_006929.5(SKIC2):c.545-127G>A rs2280774 0.24886
NM_006929.5(SKIC2):c.3212C>T (p.Ala1071Val) rs449643 0.19166
NM_006929.5(SKIC2):c.1972-42T>C rs492899 0.15022
NM_006929.5(SKIC2):c.452A>G (p.Gln151Arg) rs438999 0.11787
NM_006929.5(SKIC2):c.2202+187A>C rs9296004 0.06974
NM_006929.5(SKIC2):c.2659G>A (p.Asp887Asn) rs3911893 0.05545
NM_006929.5(SKIC2):c.3400-20C>T rs449283 0.05164
NM_006929.5(SKIC2):c.2749G>A (p.Val917Met) rs106287 0.02061
NM_006929.5(SKIC2):c.279C>G (p.Val93=) rs11541400 0.00655
NM_006929.5(SKIC2):c.3084G>A (p.Arg1028=) rs149113896 0.00446
NM_006929.5(SKIC2):c.2478+16T>A rs73729005 0.00389
NM_006929.5(SKIC2):c.2574G>A (p.Val858=) rs139281450 0.00314
NM_006929.5(SKIC2):c.2211G>A (p.Pro737=) rs2280773 0.00296
NM_006929.5(SKIC2):c.179A>G (p.Gln60Arg) rs35985869 0.00271
NM_006929.5(SKIC2):c.2880C>T (p.Ala960=) rs146035089 0.00267
NM_006929.5(SKIC2):c.2203-12A>G rs114974766 0.00222
NM_006929.5(SKIC2):c.3181-18C>T rs2075701 0.00196
NM_006929.5(SKIC2):c.1705G>A (p.Val569Met) rs144147284 0.00185
NM_006929.5(SKIC2):c.2341-16C>T rs55880341 0.00170
NM_006929.5(SKIC2):c.3666G>A (p.Leu1222=) rs142860816 0.00168
NM_006929.5(SKIC2):c.384T>C (p.Ala128=) rs3895064 0.00113
NM_006929.5(SKIC2):c.741C>G (p.Cys247Trp) rs149410050 0.00112
NM_006929.5(SKIC2):c.23-14A>T rs145129911 0.00109
NM_006929.5(SKIC2):c.3328G>C (p.Ala1110Pro) rs200525706 0.00103
NM_006929.5(SKIC2):c.774A>G (p.Glu258=) rs143738551 0.00045
NM_006929.5(SKIC2):c.2752G>A (p.Val918Ile) rs148798682 0.00024
NM_006929.5(SKIC2):c.3159T>C (p.Pro1053=) rs149774440 0.00016
NM_006929.5(SKIC2):c.585C>T (p.Asp195=) rs145042380 0.00014
NM_006929.5(SKIC2):c.3070-7T>C rs201101301 0.00011
NM_006929.5(SKIC2):c.545-6C>G rs375693076 0.00011
NM_006929.5(SKIC2):c.1860+3G>A rs547184123 0.00009
NM_006929.5(SKIC2):c.171A>G (p.Glu57=) rs746371651 0.00002
NM_006929.5(SKIC2):c.2052C>T (p.His684=) rs61761946
NM_006929.5(SKIC2):c.3180+22del rs2483003049
NM_006929.5(SKIC2):c.598+9del rs1461656830

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