ClinVar Miner

List of variants in gene COL11A2 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP
NC_000006.12:g.33170693del rs145273015
NC_000006.12:g.33192648G>T rs9277935
NM_080680.3(COL11A2):c.-174C>A rs138299820
NM_080680.3(COL11A2):c.-200G>A rs144092339
NM_080680.3(COL11A2):c.1098G>A (p.Ala366=) rs73741539
NM_080680.3(COL11A2):c.1119+42G>T rs41317102
NM_080680.3(COL11A2):c.1179+10G>A rs2744507
NM_080680.3(COL11A2):c.1360-7A>C rs3129201
NM_080680.3(COL11A2):c.1917+70G>T rs2076311
NM_080680.3(COL11A2):c.1972-16C>T rs117435723
NM_080680.3(COL11A2):c.2115+32G>T rs41317098
NM_080680.3(COL11A2):c.2136A>T (p.Gly712=) rs1799908
NM_080680.3(COL11A2):c.2214+88G>C rs2254287
NM_080680.3(COL11A2):c.2268+37T>C rs2071025
NM_080680.3(COL11A2):c.2336C>T (p.Pro779Leu) rs150877886
NM_080680.3(COL11A2):c.2430+51G>C rs2855428
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.2629-57G>A rs970902
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.2737-93T>C rs2855432
NM_080680.3(COL11A2):c.2988+57A>C rs973233
NM_080680.3(COL11A2):c.3043-65T>C rs2855434
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.3258+60C>G rs73741524
NM_080680.3(COL11A2):c.3313-11C>T rs2855437
NM_080680.3(COL11A2):c.3313-20_3313-17del rs574904915
NM_080680.3(COL11A2):c.3367-53del rs9280358
NM_080680.3(COL11A2):c.3384C>T (p.Pro1128=) rs1799911
NM_080680.3(COL11A2):c.3474+89A>G rs2855440
NM_080680.3(COL11A2):c.3529-44A>G rs16868900
NM_080680.3(COL11A2):c.3582+88A>G rs41317094
NM_080680.3(COL11A2):c.3615C>A (p.Asn1205Lys) rs141967872
NM_080680.3(COL11A2):c.3637-66G>A rs2855441
NM_080680.3(COL11A2):c.3699C>T (p.Arg1233=) rs151098305
NM_080680.3(COL11A2):c.3798+99G>A rs115196704
NM_080680.3(COL11A2):c.3852+94C>T rs2855446
NM_080680.3(COL11A2):c.3853-39G>A rs2855448
NM_080680.3(COL11A2):c.3860A>G (p.Asp1287Gly) rs142962835
NM_080680.3(COL11A2):c.3946C>A (p.Pro1316Thr) rs2229784
NM_080680.3(COL11A2):c.3960+235G>A rs73741509
NM_080680.3(COL11A2):c.4015-81G>A rs2855450
NM_080680.3(COL11A2):c.4015-82T>C rs2855449
NM_080680.3(COL11A2):c.4339-49G>T rs2855453
NM_080680.3(COL11A2):c.4392+12C>T rs117267045
NM_080680.3(COL11A2):c.4458T>A (p.Gly1486=) rs143186319
NM_080680.3(COL11A2):c.4750+286C>T rs79131379
NM_080680.3(COL11A2):c.4799G>A (p.Arg1600Gln) rs1799912
NM_080680.3(COL11A2):c.4864-64C>T rs73408005
NM_080680.3(COL11A2):c.4864-88C>T rs2744514
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.5165C>T (p.Pro1722Leu) rs2229792
NM_080680.3(COL11A2):c.799-278T>C rs3129200
NM_080680.3(COL11A2):c.826G>A (p.Glu276Lys) rs9277934
NM_080680.3(COL11A2):c.877-291G>C rs2744505
NM_080680.3(COL11A2):c.877-34C>T rs116165521
NM_080680.3(COL11A2):c.877-4T>A rs1799907

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