ClinVar Miner

List of variants in gene COL11A2 reported as benign by GeneDx

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Gene type:
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Total variants: 65
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HGVS dbSNP
NC_000006.12:g.33170693del
NC_000006.12:g.33173476T>G
NC_000006.12:g.33174143G>C
NC_000006.12:g.33192648G>T
NM_080679.2(COL11A2):c.-174C>A rs138299820
NM_080679.2(COL11A2):c.-200G>A rs144092339
NM_080679.2(COL11A2):c.1039-7A>C rs3129201
NM_080679.2(COL11A2):c.1596+70G>T
NM_080679.2(COL11A2):c.1651-16C>T rs117435723
NM_080679.2(COL11A2):c.1794+32G>T
NM_080679.2(COL11A2):c.1815A>T (p.Gly605=) rs1799908
NM_080679.2(COL11A2):c.1893+88G>C
NM_080679.2(COL11A2):c.1947+37T>C
NM_080679.2(COL11A2):c.2015C>T (p.Pro672Leu) rs150877886
NM_080679.2(COL11A2):c.2109+51G>C
NM_080679.2(COL11A2):c.2199G>A (p.Arg733=) rs117237998
NM_080679.2(COL11A2):c.2307+3G>A rs970901
NM_080679.2(COL11A2):c.2308-57G>A
NM_080679.2(COL11A2):c.2360C>T (p.Pro787Leu) rs2855430
NM_080679.2(COL11A2):c.2379T>C (p.Asp793=) rs2229785
NM_080679.2(COL11A2):c.2416-93T>C
NM_080679.2(COL11A2):c.2667+57A>C
NM_080679.2(COL11A2):c.2722-65T>C
NM_080679.2(COL11A2):c.2790G>T (p.Pro930=) rs146093235
NM_080679.2(COL11A2):c.2829+15A>C rs2855436
NM_080679.2(COL11A2):c.2853G>A (p.Pro951=) rs1799910
NM_080679.2(COL11A2):c.2937+60C>G
NM_080679.2(COL11A2):c.2992-11C>T rs2855437
NM_080679.2(COL11A2):c.3046-53del
NM_080679.2(COL11A2):c.3063C>T (p.Pro1021=) rs1799911
NM_080679.2(COL11A2):c.3153+89A>G
NM_080679.2(COL11A2):c.3208-44A>G
NM_080679.2(COL11A2):c.3261+88A>G
NM_080679.2(COL11A2):c.3294C>A (p.Asn1098Lys) rs141967872
NM_080679.2(COL11A2):c.3316-66G>A
NM_080679.2(COL11A2):c.3378C>T (p.Arg1126=) rs151098305
NM_080679.2(COL11A2):c.3477+99G>A
NM_080679.2(COL11A2):c.3531+94C>T
NM_080679.2(COL11A2):c.3532-39G>A
NM_080679.2(COL11A2):c.3539A>G (p.Asp1180Gly) rs142962835
NM_080679.2(COL11A2):c.3625C>A (p.Pro1209Thr) rs2229784
NM_080679.2(COL11A2):c.3639+235G>A
NM_080679.2(COL11A2):c.3694-81G>A
NM_080679.2(COL11A2):c.3694-82T>C
NM_080679.2(COL11A2):c.4018-49G>T
NM_080679.2(COL11A2):c.4071+12C>T rs117267045
NM_080679.2(COL11A2):c.4137T>A (p.Gly1379=) rs143186319
NM_080679.2(COL11A2):c.4429+286C>T
NM_080679.2(COL11A2):c.4478G>A (p.Arg1493Gln) rs1799912
NM_080679.2(COL11A2):c.4543-64C>T
NM_080679.2(COL11A2):c.4543-88C>T
NM_080679.2(COL11A2):c.4563G>C (p.Glu1521Asp) rs2229790
NM_080679.2(COL11A2):c.4679G>A (p.Arg1560His) rs146555195
NM_080679.2(COL11A2):c.4844C>T (p.Pro1615Leu) rs2229792
NM_080679.2(COL11A2):c.798+1282G>C
NM_080679.2(COL11A2):c.798+1539C>T
NM_080679.2(COL11A2):c.798+1569T>A rs1799907
NM_080679.2(COL11A2):c.798+2461G>A rs73741539
NM_080679.2(COL11A2):c.798+2524G>T
NM_080679.2(COL11A2):c.798+571T>C
NM_080679.2(COL11A2):c.798+876G>A rs9277934
NM_080679.2(COL11A2):c.858+10G>A rs2744507
NM_080680.2(COL11A2):c.2431-18delC rs9280359
NM_080680.2(COL11A2):c.2484+13delG rs55730247
NM_080680.2(COL11A2):c.3313-20_3313-17delGACT rs574904915

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