ClinVar Miner

Variants in gene COL11A2 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 41
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HGVS dbSNP
NM_080680.3(COL11A2):c.*4C>T rs186720023
NM_080680.3(COL11A2):c.-200G>A rs144092339
NM_080680.3(COL11A2):c.1098G>A (p.Ala366=) rs73741539
NM_080680.3(COL11A2):c.1612-10G>C rs182657680
NM_080680.3(COL11A2):c.1615C>T (p.Arg539Trp) rs145499142
NM_080680.3(COL11A2):c.1666-11CCT[2] rs147815324
NM_080680.3(COL11A2):c.1774-9C>T rs148243956
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.2017-5T>G rs200523422
NM_080680.3(COL11A2):c.2115+7T>C rs186051366
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.2520G>A (p.Arg840=) rs117237998
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.329G>A (p.Arg110Gln) rs145960317
NM_080680.3(COL11A2):c.353G>C (p.Arg118Pro) rs41268014
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.390G>C (p.Arg130=) rs149638770
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.4683A>G (p.Thr1561=) rs34055850
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.4950C>T (p.Asp1650=) rs372110441
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

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