ClinVar Miner

List of variants in gene ADAMTS2 reported as likely benign by Invitae

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 99
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HGVS dbSNP
NM_014244.5(ADAMTS2):c.1008T>C (p.Ser336=) rs1581160048
NM_014244.5(ADAMTS2):c.1080C>T (p.His360=) rs777406209
NM_014244.5(ADAMTS2):c.1083T>C (p.Asp361=) rs150079799
NM_014244.5(ADAMTS2):c.1133-10C>T rs934418118
NM_014244.5(ADAMTS2):c.1149C>T (p.Thr383=) rs199664723
NM_014244.5(ADAMTS2):c.1164G>A (p.Pro388=) rs141348218
NM_014244.5(ADAMTS2):c.1239-5C>T rs767804420
NM_014244.5(ADAMTS2):c.1254C>T (p.His418=) rs758041605
NM_014244.5(ADAMTS2):c.1383-5C>G rs1447276433
NM_014244.5(ADAMTS2):c.139+4G>A rs1023653032
NM_014244.5(ADAMTS2):c.1413C>T (p.Phe471=) rs751565994
NM_014244.5(ADAMTS2):c.1414G>A (p.Ala472Thr) rs546681307
NM_014244.5(ADAMTS2):c.1431G>A (p.Ala477=) rs147259971
NM_014244.5(ADAMTS2):c.1467C>T (p.Asn489=) rs111893309
NM_014244.5(ADAMTS2):c.1501A>G (p.Met501Val) rs757394676
NM_014244.5(ADAMTS2):c.1524C>A (p.Thr508=) rs778841966
NM_014244.5(ADAMTS2):c.161C>T (p.Ala54Val) rs368221089
NM_014244.5(ADAMTS2):c.1707G>A (p.Pro569=) rs749970172
NM_014244.5(ADAMTS2):c.1824G>A (p.Gln608=) rs1581147040
NM_014244.5(ADAMTS2):c.1848C>T (p.Pro616=) rs569510744
NM_014244.5(ADAMTS2):c.1869C>T (p.Arg623=) rs376058580
NM_014244.5(ADAMTS2):c.1914C>T (p.Asp638=) rs752737484
NM_014244.5(ADAMTS2):c.2015G>T (p.Arg672Leu) rs200806292
NM_014244.5(ADAMTS2):c.2034G>A (p.Thr678=) rs139943837
NM_014244.5(ADAMTS2):c.2109C>T (p.Ile703=) rs200210415
NM_014244.5(ADAMTS2):c.2145C>T (p.Cys715=) rs372661052
NM_014244.5(ADAMTS2):c.2244C>T (p.Ala748=) rs1581143017
NM_014244.5(ADAMTS2):c.2267T>C (p.Val756Ala) rs141650732
NM_014244.5(ADAMTS2):c.2291-10C>T rs753601981
NM_014244.5(ADAMTS2):c.2292C>T (p.Ala764=) rs188566209
NM_014244.5(ADAMTS2):c.2376C>T (p.Gly792=) rs779908624
NM_014244.5(ADAMTS2):c.237G>A (p.Thr79=) rs753133442
NM_014244.5(ADAMTS2):c.2403C>T (p.Asp801=) rs374315892
NM_014244.5(ADAMTS2):c.241A>C (p.Arg81=) rs936171876
NM_014244.5(ADAMTS2):c.2451C>T (p.Thr817=) rs138564815
NM_014244.5(ADAMTS2):c.2458-10del rs748892203
NM_014244.5(ADAMTS2):c.2466G>T (p.Pro822=) rs377085746
NM_014244.5(ADAMTS2):c.2469G>A (p.Val823=) rs182103023
NM_014244.5(ADAMTS2):c.2472A>C (p.Gly824=) rs1581140650
NM_014244.5(ADAMTS2):c.2487A>C (p.Ser829=) rs201592583
NM_014244.5(ADAMTS2):c.2545C>T (p.Leu849=) rs1581140577
NM_014244.5(ADAMTS2):c.2613C>T (p.Gly871=) rs145016043
NM_014244.5(ADAMTS2):c.273G>C (p.Pro91=) rs768036305
NM_014244.5(ADAMTS2):c.2742C>G (p.Ser914=) rs567635584
NM_014244.5(ADAMTS2):c.2750+10C>T rs1045751866
NM_014244.5(ADAMTS2):c.2795G>A (p.Arg932Gln) rs140022033
NM_014244.5(ADAMTS2):c.2811G>A (p.Val937=) rs557019144
NM_014244.5(ADAMTS2):c.2817C>T (p.Ser939=) rs201215425
NM_014244.5(ADAMTS2):c.2835G>A (p.Pro945=) rs768390657
NM_014244.5(ADAMTS2):c.2841C>T (p.His947=) rs779661341
NM_014244.5(ADAMTS2):c.2865C>T (p.His955=) rs752790963
NM_014244.5(ADAMTS2):c.2883C>T (p.Asp961=) rs370397254
NM_014244.5(ADAMTS2):c.2892C>T (p.Pro964=) rs546361762
NM_014244.5(ADAMTS2):c.2893G>A (p.Glu965Lys) rs144138766
NM_014244.5(ADAMTS2):c.2961C>T (p.Cys987=) rs1581137330
NM_014244.5(ADAMTS2):c.2979C>T (p.Asn993=) rs747970179
NM_014244.5(ADAMTS2):c.2991G>A (p.Glu997=) rs1581137308
NM_014244.5(ADAMTS2):c.2994G>T (p.Arg998=) rs780314895
NM_014244.5(ADAMTS2):c.3012C>G (p.Thr1004=) rs571054777
NM_014244.5(ADAMTS2):c.3012C>T (p.Thr1004=) rs571054777
NM_014244.5(ADAMTS2):c.3018C>T (p.Asp1006=) rs150535792
NM_014244.5(ADAMTS2):c.3027C>T (p.Phe1009=) rs766033559
NM_014244.5(ADAMTS2):c.3060G>A (p.Ala1020=) rs61754844
NM_014244.5(ADAMTS2):c.3078C>A (p.Gly1026=) rs886060491
NM_014244.5(ADAMTS2):c.312G>A (p.Glu104=) rs781264319
NM_014244.5(ADAMTS2):c.3174G>A (p.Ser1058=) rs1167217144
NM_014244.5(ADAMTS2):c.3249A>C (p.Pro1083=) rs1581132628
NM_014244.5(ADAMTS2):c.3291C>T (p.Asn1097=) rs1581132604
NM_014244.5(ADAMTS2):c.3303C>T (p.Asn1101=) rs766731589
NM_014244.5(ADAMTS2):c.3342C>T (p.Asn1114=) rs79606317
NM_014244.5(ADAMTS2):c.3351C>T (p.Asp1117=) rs777279065
NM_014244.5(ADAMTS2):c.339C>T (p.Val113=) rs143877087
NM_014244.5(ADAMTS2):c.3551C>T (p.Pro1184Leu) rs150989902
NM_014244.5(ADAMTS2):c.3552G>A (p.Pro1184=) rs185794582
NM_014244.5(ADAMTS2):c.3597T>C (p.Ile1199=) rs1245816073
NM_014244.5(ADAMTS2):c.3624C>T (p.Leu1208=) rs139420412
NM_014244.5(ADAMTS2):c.3627A>G (p.Gly1209=) rs1290092850
NM_014244.5(ADAMTS2):c.396G>T (p.Ala132=) rs770621969
NM_014244.5(ADAMTS2):c.42C>G (p.Pro14=) rs1581302053
NM_014244.5(ADAMTS2):c.48G>A (p.Leu16=) rs1342781405
NM_014244.5(ADAMTS2):c.492A>G (p.Leu164=) rs1581299393
NM_014244.5(ADAMTS2):c.513G>T (p.Ala171=) rs369983319
NM_014244.5(ADAMTS2):c.525C>T (p.Cys175=) rs140167371
NM_014244.5(ADAMTS2):c.535-4G>A rs765017540
NM_014244.5(ADAMTS2):c.535-5C>T rs772473736
NM_014244.5(ADAMTS2):c.580T>C (p.Leu194=) rs1554094148
NM_014244.5(ADAMTS2):c.600G>A (p.Ala200=) rs761444202
NM_014244.5(ADAMTS2):c.651G>A (p.Thr217=) rs138580383
NM_014244.5(ADAMTS2):c.654C>G (p.Ser218=) rs1581236091
NM_014244.5(ADAMTS2):c.732C>T (p.Gly244=) rs143069972
NM_014244.5(ADAMTS2):c.748G>A (p.Ala250Thr) rs143764421
NM_014244.5(ADAMTS2):c.759G>A (p.Ser253=) rs374180760
NM_014244.5(ADAMTS2):c.762G>A (p.Arg254=) rs753246905
NM_014244.5(ADAMTS2):c.814C>T (p.Leu272=) rs531768193
NM_014244.5(ADAMTS2):c.891+9G>A rs749508251
NM_014244.5(ADAMTS2):c.927C>T (p.Ala309=) rs143588140
NM_014244.5(ADAMTS2):c.94C>T (p.Pro32Ser) rs547548078
NM_014244.5(ADAMTS2):c.975+9A>G rs1581171879
NM_014244.5(ADAMTS2):c.990C>T (p.Ile330=) rs543342610

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