ClinVar Miner

List of variants in gene ADAMTS10 reported as uncertain significance for Weill-Marchesani syndrome

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NM_030957.4(ADAMTS10):c.*322C>T rs886054708
NM_030957.4(ADAMTS10):c.*36T>C rs782348033
NM_030957.4(ADAMTS10):c.*411C>T rs886054707
NM_030957.4(ADAMTS10):c.*449G>C rs555471852
NM_030957.4(ADAMTS10):c.*456del rs34057037
NM_030957.4(ADAMTS10):c.*456dup rs34057037
NM_030957.4(ADAMTS10):c.*81G>T rs886054709
NM_030957.4(ADAMTS10):c.*85dup rs576948646
NM_030957.4(ADAMTS10):c.-143G>C rs886054716
NM_030957.4(ADAMTS10):c.-60G>A rs573082154
NM_030957.4(ADAMTS10):c.1085-5C>T rs781831794
NM_030957.4(ADAMTS10):c.1176C>T (p.His392=) rs371013844
NM_030957.4(ADAMTS10):c.1530C>G (p.Thr510=) rs886054715
NM_030957.4(ADAMTS10):c.1568C>T (p.Thr523Met) rs782308360
NM_030957.4(ADAMTS10):c.1569G>A (p.Thr523=) rs150203950
NM_030957.4(ADAMTS10):c.1794G>C (p.Thr598=) rs145420448
NM_030957.4(ADAMTS10):c.1880A>C (p.Lys627Thr) rs782712334
NM_030957.4(ADAMTS10):c.1920G>A (p.Ser640=) rs142602984
NM_030957.4(ADAMTS10):c.1935G>A (p.Ala645=) rs200551849
NM_030957.4(ADAMTS10):c.1987C>A (p.Pro663Thr) rs886054714
NM_030957.4(ADAMTS10):c.1994G>A (p.Arg665His) rs370179236
NM_030957.4(ADAMTS10):c.2005G>T (p.Val669Leu) rs144596955
NM_030957.4(ADAMTS10):c.2125G>A (p.Glu709Lys) rs550588972
NM_030957.4(ADAMTS10):c.2220C>T (p.Asn740=) rs886054713
NM_030957.4(ADAMTS10):c.2239+10T>C rs782597342
NM_030957.4(ADAMTS10):c.2261C>T (p.Ser754Phe) rs142353301
NM_030957.4(ADAMTS10):c.2409G>C (p.Leu803=) rs61757472
NM_030957.4(ADAMTS10):c.2433C>T (p.Leu811=) rs886054712
NM_030957.4(ADAMTS10):c.2530+9G>A rs782625211
NM_030957.4(ADAMTS10):c.303C>T (p.His101=) rs141630862
NM_030957.4(ADAMTS10):c.3043-8C>T rs759098979
NM_030957.4(ADAMTS10):c.3159T>C (p.Cys1053=) rs886054711
NM_030957.4(ADAMTS10):c.3202+13C>T rs886054710
NM_030957.4(ADAMTS10):c.3268G>A (p.Ala1090Thr) rs782053556
NM_030957.4(ADAMTS10):c.350C>T (p.Ala117Val) rs141952128
NM_030957.4(ADAMTS10):c.613C>T (p.Arg205Trp) rs147270233
NM_030957.4(ADAMTS10):c.641C>G (p.Pro214Arg) rs1555741490
NM_030957.4(ADAMTS10):c.834G>A (p.Ser278=) rs782449192

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