ClinVar Miner

List of variants in gene COL11A2 reported as likely benign for not provided

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Total variants: 39
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HGVS dbSNP
NM_080680.3(COL11A2):c.1188C>T (p.Leu396=) rs532305958
NM_080680.3(COL11A2):c.1285-58A>G rs115849873
NM_080680.3(COL11A2):c.1665+17C>T rs543296211
NM_080680.3(COL11A2):c.1698C>T (p.Leu566=) rs139350991
NM_080680.3(COL11A2):c.1806G>A (p.Leu602=) rs1583343003
NM_080680.3(COL11A2):c.1818+42G>A rs73741534
NM_080680.3(COL11A2):c.1875C>T (p.Gly625=) rs141815296
NM_080680.3(COL11A2):c.1971+20C>T rs770912127
NM_080680.3(COL11A2):c.1980C>T (p.Pro660=) rs2229786
NM_080680.3(COL11A2):c.2017-5T>G rs200523422
NM_080680.3(COL11A2):c.2085G>A (p.Lys695=) rs368770525
NM_080680.3(COL11A2):c.2116-8T>C rs778098198
NM_080680.3(COL11A2):c.2187G>C (p.Arg729=) rs551411073
NM_080680.3(COL11A2):c.2336C>T (p.Pro779Leu) rs150877886
NM_080680.3(COL11A2):c.3043-10G>A rs1583313311
NM_080680.3(COL11A2):c.353G>C (p.Arg118Pro) rs41268014
NM_080680.3(COL11A2):c.3583-5T>C rs183536190
NM_080680.3(COL11A2):c.3616C>T (p.Leu1206=) rs147576338
NM_080680.3(COL11A2):c.3636+74G>C rs45596935
NM_080680.3(COL11A2):c.3690+9C>T rs1397368233
NM_080680.3(COL11A2):c.3974C>T (p.Ser1325Leu) rs543145528
NM_080680.3(COL11A2):c.3975G>A (p.Ser1325=) rs139564431
NM_080680.3(COL11A2):c.3999A>G (p.Gly1333=) rs201392156
NM_080680.3(COL11A2):c.4206C>T (p.Gly1402=) rs201642192
NM_080680.3(COL11A2):c.4265C>T (p.Pro1422Leu) rs555936333
NM_080680.3(COL11A2):c.4323G>A (p.Gly1441=) rs1476202918
NM_080680.3(COL11A2):c.4344C>A (p.Ile1448=) rs554269032
NM_080680.3(COL11A2):c.4393-28C>T rs144062635
NM_080680.3(COL11A2):c.4751-9A>G rs555680585
NM_080680.3(COL11A2):c.4821A>C (p.Ala1607=) rs749261447
NM_080680.3(COL11A2):c.4863+7G>A rs200947059
NM_080680.3(COL11A2):c.4864-32_4864-7del rs767389906
NM_080680.3(COL11A2):c.5000G>A (p.Arg1667His) rs146555195
NM_080680.3(COL11A2):c.579C>T (p.Ala193=) rs201054429
NM_080680.3(COL11A2):c.606+11C>T rs368302768
NM_080680.3(COL11A2):c.83-55A>T rs56297647
NM_080680.3(COL11A2):c.876+128T>C rs139969885
NM_080680.3(COL11A2):c.876+31C>T rs113453266
NM_080680.3(COL11A2):c.882C>T (p.Pro294=) rs566296770

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