ClinVar Miner

List of variants in gene COL11A1 reported as benign for not specified

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Gene type:
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Total variants: 57
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HGVS dbSNP
NM_001854.3(COL11A1):c.1308+19A>G rs34587338
NM_001854.3(COL11A1):c.130G>A (p.Ala44Thr) rs150090939
NM_001854.3(COL11A1):c.138T>G (p.Asp46Glu) rs11164663
NM_001854.3(COL11A1):c.1413+18A>T rs17461252
NM_001854.3(COL11A1):c.1792-12_1792-10delATG rs71752747
NM_001854.3(COL11A1):c.1792-15_1792-10delATGATG rs71752747
NM_001854.3(COL11A1):c.1872A>G (p.Pro624=) rs111841420
NM_001854.3(COL11A1):c.1944+11T>C rs71664954
NM_001854.3(COL11A1):c.1998+4T>A rs12136577
NM_001854.3(COL11A1):c.2043+8G>A rs2622875
NM_001854.3(COL11A1):c.2097+18C>A rs75124465
NM_001854.3(COL11A1):c.2578T>A (p.Phe860Ile) rs141548164
NM_001854.3(COL11A1):c.2611-19A>C rs11164649
NM_001854.3(COL11A1):c.2611-4C>T rs79505593
NM_001854.3(COL11A1):c.2656-28T>C rs1903787
NM_001854.3(COL11A1):c.274+42G>C rs11164662
NM_001854.3(COL11A1):c.275-7T>C rs12136865
NM_001854.3(COL11A1):c.2766A>G (p.Gly922=) rs139911745
NM_001854.3(COL11A1):c.2901A>C (p.Gly967=) rs149526015
NM_001854.3(COL11A1):c.3025-23A>T rs55682104
NM_001854.3(COL11A1):c.3033A>C (p.Pro1011=) rs143606220
NM_001854.3(COL11A1):c.3168+15A>G rs1012281
NM_001854.3(COL11A1):c.3168+41T>C rs1012282
NM_001854.3(COL11A1):c.3169-16T>C rs76379510
NM_001854.3(COL11A1):c.3375C>T (p.Asp1125=) rs17127270
NM_001854.3(COL11A1):c.3817-13_3817-12insT rs34228277
NM_001854.3(COL11A1):c.3817-13delT rs34228277
NM_001854.3(COL11A1):c.3817-14_3817-13dupTT rs34228277
NM_001854.3(COL11A1):c.3817-17_3817-16insC rs773173330
NM_001854.3(COL11A1):c.3817-5T>C rs201155391
NM_001854.3(COL11A1):c.3924+19C>T rs77901108
NM_001854.3(COL11A1):c.3968C>T (p.Pro1323Leu) rs3753841
NM_001854.3(COL11A1):c.3978+38T>G rs28648038
NM_001854.3(COL11A1):c.3979-14A>T rs186245518
NM_001854.3(COL11A1):c.3979-3T>C rs138464908
NM_001854.3(COL11A1):c.4140+10A>T rs187171126
NM_001854.3(COL11A1):c.4140+13T>A rs374901069
NM_001854.3(COL11A1):c.4303-13delT rs35232764
NM_001854.3(COL11A1):c.4303-47T>C rs11164634
NM_001854.3(COL11A1):c.4468A>G (p.Ile1490Val) rs145901197
NM_001854.3(COL11A1):c.4512T>C (p.Gly1504=) rs1763347
NM_001854.3(COL11A1):c.4603T>C (p.Ser1535Pro) rs1676486
NM_001854.3(COL11A1):c.4606C>G (p.Pro1536Ala) rs139064549
NM_001854.3(COL11A1):c.4608+18A>G rs17127203
NM_001854.3(COL11A1):c.4701T>C (p.Asp1567=) rs138691968
NM_001854.3(COL11A1):c.4770T>C (p.Ile1590=) rs2229783
NM_001854.3(COL11A1):c.488+23G>A rs6668897
NM_001854.3(COL11A1):c.4965T>G (p.Ser1655=) rs74778421
NM_001854.3(COL11A1):c.651+16A>G rs116303092
NM_001854.3(COL11A1):c.652-6dupT rs36076089
NM_001854.3(COL11A1):c.652-7_652-6delTT rs36076089
NM_001854.3(COL11A1):c.660T>C (p.Ile220=) rs71664966
NM_001854.3(COL11A1):c.904A>G (p.Ile302Val) rs75824519
NM_080629.2(COL11A1):c.2179-10dupT rs747240373
NM_080629.2(COL11A1):c.2331+37A>T rs2622867
NM_080629.2(COL11A1):c.52A>T (p.Thr18Ser)
NM_080629.2(COL11A1):c.652-6delT rs36076089

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