ClinVar Miner

List of variants in gene COL11A2 reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP
NM_080680.3(COL11A2):c.*4C>T rs186720023
NM_080680.3(COL11A2):c.1098G>A (p.Ala366=) rs73741539
NM_080680.3(COL11A2):c.1179+10G>A rs2744507
NM_080680.3(COL11A2):c.1360-7A>C rs3129201
NM_080680.3(COL11A2):c.1666-11CCT[2] rs147815324
NM_080680.3(COL11A2):c.1666-9T>G rs181999673
NM_080680.3(COL11A2):c.1782C>T (p.Asp594=) rs41266697
NM_080680.3(COL11A2):c.1819-10G>A rs3129202
NM_080680.3(COL11A2):c.1875C>T (p.Gly625=) rs141815296
NM_080680.3(COL11A2):c.1972-16C>T rs117435723
NM_080680.3(COL11A2):c.2017-5T>G rs200523422
NM_080680.3(COL11A2):c.2115+7T>C rs186051366
NM_080680.3(COL11A2):c.2136A>T (p.Gly712=) rs1799908
NM_080680.3(COL11A2):c.2186G>A (p.Arg729Gln) rs61730262
NM_080680.3(COL11A2):c.230C>A (p.Pro77Gln) rs35765893
NM_080680.3(COL11A2):c.2336C>T (p.Pro779Leu) rs150877886
NM_080680.3(COL11A2):c.2431-18del rs9280359
NM_080680.3(COL11A2):c.2484+13del rs55730247
NM_080680.3(COL11A2):c.2484+22C>G rs2744512
NM_080680.3(COL11A2):c.2520G>A (p.Arg840=) rs117237998
NM_080680.3(COL11A2):c.2628+3G>A rs970901
NM_080680.3(COL11A2):c.2681C>T (p.Pro894Leu) rs2855430
NM_080680.3(COL11A2):c.2682+26A>C rs9277932
NM_080680.3(COL11A2):c.2700T>C (p.Asp900=) rs2229785
NM_080680.3(COL11A2):c.2757C>T (p.Gly919=) rs34478777
NM_080680.3(COL11A2):c.2899-9del rs397517477
NM_080680.3(COL11A2):c.3111G>T (p.Pro1037=) rs146093235
NM_080680.3(COL11A2):c.3150+15A>C rs2855436
NM_080680.3(COL11A2):c.3174G>A (p.Pro1058=) rs1799910
NM_080680.3(COL11A2):c.329G>A (p.Arg110Gln) rs145960317
NM_080680.3(COL11A2):c.3313-11C>T rs2855437
NM_080680.3(COL11A2):c.3313-20_3313-17del rs574904915
NM_080680.3(COL11A2):c.3384C>T (p.Pro1128=) rs1799911
NM_080680.3(COL11A2):c.3583-5T>C rs183536190
NM_080680.3(COL11A2):c.3615C>A (p.Asn1205Lys) rs141967872
NM_080680.3(COL11A2):c.3699C>T (p.Arg1233=) rs151098305
NM_080680.3(COL11A2):c.3860A>G (p.Asp1287Gly) rs142962835
NM_080680.3(COL11A2):c.390G>C (p.Arg130=) rs149638770
NM_080680.3(COL11A2):c.3946C>A (p.Pro1316Thr) rs2229784
NM_080680.3(COL11A2):c.3975G>A (p.Ser1325=) rs139564431
NM_080680.3(COL11A2):c.4041G>A (p.Pro1347=) rs139283268
NM_080680.3(COL11A2):c.4265C>T (p.Pro1422Leu) rs555936333
NM_080680.3(COL11A2):c.4383C>T (p.Pro1461=) rs148262058
NM_080680.3(COL11A2):c.4392+12C>T rs117267045
NM_080680.3(COL11A2):c.4458T>A (p.Gly1486=) rs143186319
NM_080680.3(COL11A2):c.4521G>A (p.Gln1507=) rs114580597
NM_080680.3(COL11A2):c.4799G>A (p.Arg1600Gln) rs1799912
NM_080680.3(COL11A2):c.4863+7G>A rs200947059
NM_080680.3(COL11A2):c.4884G>C (p.Glu1628Asp) rs2229790
NM_080680.3(COL11A2):c.5000G>A (p.Arg1667His) rs146555195
NM_080680.3(COL11A2):c.5071-5T>G rs368309085
NM_080680.3(COL11A2):c.5165C>T (p.Pro1722Leu) rs2229792
NM_080680.3(COL11A2):c.688G>T (p.Gly230Trp) rs141430703
NM_080680.3(COL11A2):c.798+38C>A rs200989046
NM_080680.3(COL11A2):c.826G>A (p.Glu276Lys) rs9277934
NM_080680.3(COL11A2):c.877-4T>A rs1799907

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