ADAMTS10[gene] - ClinVar - NCBI

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VariationLocation		Gene(s)	Protein change	Condition(s)	Clinical significance (Last reviewed)	Review status
Select item 590821.	GRCh38/hg38 19p13.3-13.2(chr19:1972245-9648879)x3 GRCh37: Chr19:1972244-9759555 GRCh38: Chr19:1972245-9648879	ACER1, ACSBG2, ACTL9, ADAMTS10, ADGRE1, ALKBH7, AMH, ANGPTL4, ANKRD24, AP3D1, APBA3, ARHGEF18, ARRDC5, ATCAY, BTBD2, C3, CACTIN, CACTIN-AS1, CAMSAP3, CAPS, CATSPERD, CCL25, CD209, CD320, CD70, CELF5, CERS4, CHAF1A, CLEC4G, CLEC4M, CLPP, CRB3, CREB3L3, CSNK1G2, CTXN1, DAPK3, DENND1C, DIRAS1, DOHH, DOT1L, DPP9, DPP9-AS1, DUS3L, EBI3, EEF2, ELAVL1, EVI5L, FBN3, FCER2, FEM1A, FSD1, FUT3, FUT5, FUT6, FZR1, GADD45B, GIPC3, GNA11, GNA15, GNA15-DT, GNG7, GPR108, GTF2F1, HDGFL2, HMG20B, HNRNPM, HSD11B1L, INSR, IZUMO4, JSRP1, KANK3, KDM4B, KHSRP, LINC01775, LINGO3, LMNB2, LOC100128573, LOC101928844, LOC106804547, LOC108348031, LOC108783649, LOC111413022, LOC111556134, LOC111721712, LOC111828491, LOC111828492, LOC111828495, LOC112543475, LOC112543476, LOC112543477, LOC112543480, LOC112543481, LOC112543482, LOC112543490, LOC112552148, LOC112552174, LOC112552175, LOC112552176, LOC112577455, LOC112577456, LOC112577457, LOC112577458, LOC113939970, LOC113939971, LOC113939974, LOC113939976, LOC116276497, LOC116276498, LOC116276499, LOC116276500, LOC117282006, LOC117307477, LOC117307478, LOC121627846, LOC121627847, LOC121627848, LOC121627849, LOC121627850, LOC121627851, LOC121627852, LOC121627853, LOC121627854, LOC121627855, LOC121852972, LOC121852973, LOC121852974, LOC121852975, LOC121852976, LOC125371450, LOC125371451, LOC125371452, LOC125371453, LOC125371455, LOC125371457, LOC125371459, LOC125371460, LOC125371461, LOC125371462, LOC125371463, LOC125371464, LOC125371465, LOC125371466, LOC125371467, LOC125371468, LOC125371469, LOC125371470, LOC125371471, LOC125371472, LOC125371473, LOC126862839, LOC126862840, LOC126862841, LOC126862842, LOC126862843, LOC126862844, LOC126862845, LOC126862846, LOC126862847, LOC126862848, LOC126862849, LOC126862850, LOC128772422, LOC128772423, LOC128772424, LOC390877, LONP1, LRG1, LRRC8E, LSM7, MAP2K2, MAP2K7, MARCHF2, MATK, MBD3L1, MBD3L2, MBD3L2B, MBD3L3, MBD3L4, MBD3L5, MCEMP1, MCOLN1, MFSD12, MICOS13, MIR1227, MIR3940, MIR4321, MIR4746, MIR4747, MIR4999, MIR637, MIR6789, MIR6790, MIR6791, MIR6792, MIR6885, MIR7-3, MIR7-3HG, MIR7108, MIR7850, MKNK2, MLLT1, MOB3A, MPND, MRPL54, MUC16, MYDGF, MYO1F, NCLN, NDUFA11, NDUFA7, NFIC, NFILZ, NMRK2, NRTN, OAZ1, OR1M1, OR2Z1, OR7D2, OR7D4, OR7E24, OR7G1, OR7G2, OR7G3, PCP2, PEAK3, PET100, PEX11G, PIAS4, PIP5K1C, PLEKHJ1, PLIN3, PLIN4, PLIN5, PNPLA6, PRAM1, PRR22, PRR36, PSPN, PTPRS, RAB11B, RAB11B-AS1, RANBP3, RANBP3-DT, RAX2, RETN, RFX2, RPL36, RPS28, S1PR4, SAFB, SAFB2, SEMA6B, SF3A2, SGTA, SH2D3A, SH3GL1, SHD, SIRT6, SLC25A23, SLC25A41, SLC39A3, SMIM24, SMIM44, SNAPC2, SNORD37, SPPL2B, STAP2, STXBP2, TBXA2R, TEKTIP1, TEX45, TGFBR3L, THOP1, TICAM1, TIMM13, TIMM44, TINCR, TJP3, TLE2, TLE5, TLE6, TMIGD2, TMPRSS9, TNFAIP8L1, TNFSF14, TNFSF9, TRAPPC5, TRG-TCC1-1, TRIP10, TRV-CAC3-1, TUBB4A, UBXN6, UHRF1, VAV1, VMAC, XAB2, YJU2, ZBTB7A, ZFR2, ZNF121, ZNF177, ZNF266, ZNF317, ZNF358, ZNF414, ZNF426, ZNF426-DT, ZNF554, ZNF555, ZNF556, ZNF557, ZNF558, ZNF559, ZNF559-ZNF177, ZNF560, ZNF561, ZNF561-AS1, ZNF562, ZNF57, ZNF699, ZNF77, ZNRF4		See cases	Pathogenic (Aug 12, 2011)	criteria provided, single submitter
Select item 5452282.	Single allele GRCh38: Chr19:7981357-10019383	ACTL9, ADAMTS10, ANGPTL4, CCL25, CD320, CERS4, COL5A3, ELAVL1, FBN3, FBXL12, HNRNPM, KANK3, LOC100505555, LOC111413022, LOC112577458, LOC121627855, LOC125371470, LOC125371471, LOC125371472, LOC125371473, LOC125371474, LOC126862848, LOC126862849, LOC126862850, LOC126862851, LOC126862852, MARCHF2, MBD3L1, MIR4999, MUC16, MYO1F, NDUFA7, NFILZ, OLFM2, OR1M1, OR2Z1, OR7D2, OR7D4, OR7E24, OR7G1, OR7G2, OR7G3, PIN1, PIN1-DT, PRAM1, RAB11B, RAB11B-AS1, RDH8, RPS28, UBL5, ZNF121, ZNF177, ZNF266, ZNF317, ZNF414, ZNF426, ZNF426-DT, ZNF558, ZNF559, ZNF559-ZNF177, ZNF560, ZNF561, ZNF561-AS1, ZNF562, ZNF699, ZNF846		Autism	Likely pathogenic (Mar 20, 2018)	criteria provided, single submitter
Select item 8927683.	NM_030957.4(ADAMTS10):c.*630C>T GRCh37: Chr19:8645147 GRCh38: Chr19:8580263	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 12, 2018)	criteria provided, single submitter
Select item 8927694.	NM_030957.4(ADAMTS10):c.*578C>A GRCh37: Chr19:8645199 GRCh38: Chr19:8580315	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 13, 2018)	criteria provided, single submitter
Select item 8927705.	NM_030957.4(ADAMTS10):c.*563C>A GRCh37: Chr19:8645214 GRCh38: Chr19:8580330	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 13, 2018)	criteria provided, single submitter
Select item 3305666.	NM_030957.4(ADAMTS10):c.*456dup GRCh37: Chr19:8645320-8645321 GRCh38: Chr19:8580436-8580437	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jun 14, 2016)	criteria provided, single submitter
Select item 3305677.	NM_030957.4(ADAMTS10):c.*456del GRCh37: Chr19:8645321 GRCh38: Chr19:8580437	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jun 14, 2016)	criteria provided, single submitter
Select item 3305688.	NM_030957.4(ADAMTS10):c.*449G>C GRCh37: Chr19:8645328 GRCh38: Chr19:8580444	ADAMTS10		Weill-Marchesani syndrome	Benign (Jan 12, 2018)	criteria provided, single submitter
Select item 8927719.	NM_030957.4(ADAMTS10):c.*447G>T GRCh37: Chr19:8645330 GRCh38: Chr19:8580446	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 13, 2018)	criteria provided, single submitter
Select item 33056910.	NM_030957.4(ADAMTS10):c.*428A>G GRCh37: Chr19:8645349 GRCh38: Chr19:8580465	ADAMTS10		Weill-Marchesani syndrome	Benign (Jan 13, 2018)	criteria provided, single submitter
Select item 33057011.	NM_030957.4(ADAMTS10):c.*411C>T GRCh37: Chr19:8645366 GRCh38: Chr19:8580482	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 12, 2018)	criteria provided, single submitter
Select item 89357412.	NM_030957.4(ADAMTS10):c.*356G>A GRCh37: Chr19:8645421 GRCh38: Chr19:8580537	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 13, 2018)	criteria provided, single submitter
Select item 89357513.	NM_030957.4(ADAMTS10):c.*330A>T GRCh37: Chr19:8645447 GRCh38: Chr19:8580563	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 13, 2018)	criteria provided, single submitter
Select item 33057114.	NM_030957.4(ADAMTS10):c.*322C>T GRCh37: Chr19:8645455 GRCh38: Chr19:8580571	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 12, 2018)	criteria provided, single submitter
Select item 89357615.	NM_030957.4(ADAMTS10):c.*311A>G GRCh37: Chr19:8645466 GRCh38: Chr19:8580582	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 13, 2018)	criteria provided, single submitter
Select item 89357716.	NM_030957.4(ADAMTS10):c.*259G>A GRCh37: Chr19:8645518 GRCh38: Chr19:8580634	ADAMTS10		Weill-Marchesani syndrome, not provided	Benign/Likely benign (Apr 12, 2019)	criteria provided, multiple submitters, no conflicts
Select item 33057217.	NM_030957.4(ADAMTS10):c.*238dup GRCh37: Chr19:8645538-8645539 GRCh38: Chr19:8580654-8580655	ADAMTS10		Weill-Marchesani syndrome, not provided	Benign/Likely benign (Jul 31, 2018)	criteria provided, multiple submitters, no conflicts
Select item 89357818.	NM_030957.4(ADAMTS10):c.*209C>T GRCh37: Chr19:8645568 GRCh38: Chr19:8580684	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 13, 2018)	criteria provided, single submitter
Select item 89357919.	NM_030957.4(ADAMTS10):c.*171G>A GRCh37: Chr19:8645606 GRCh38: Chr19:8580722	ADAMTS10		Weill-Marchesani syndrome, not provided	Likely benign (Aug 20, 2018)	criteria provided, multiple submitters, no conflicts
Select item 89358020.	NM_030957.4(ADAMTS10):c.*157G>A GRCh37: Chr19:8645620 GRCh38: Chr19:8580736	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 12, 2018)	criteria provided, single submitter
Select item 89386521.	NM_030957.4(ADAMTS10):c.*146G>A GRCh37: Chr19:8645631 GRCh38: Chr19:8580747	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 12, 2018)	criteria provided, single submitter
Select item 33057322.	NM_030957.4(ADAMTS10):c.*85dup GRCh37: Chr19:8645691-8645692 GRCh38: Chr19:8580807-8580808	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jun 14, 2016)	criteria provided, single submitter
Select item 89386623.	NM_030957.4(ADAMTS10):c.*81G>C GRCh37: Chr19:8645696 GRCh38: Chr19:8580812	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 12, 2018)	criteria provided, single submitter
Select item 33057424.	NM_030957.4(ADAMTS10):c.*81G>T GRCh37: Chr19:8645696 GRCh38: Chr19:8580812	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 12, 2018)	criteria provided, single submitter
Select item 89386725.	NM_030957.4(ADAMTS10):c.*47A>G GRCh37: Chr19:8645730 GRCh38: Chr19:8580846	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 13, 2018)	criteria provided, single submitter
Select item 33057526.	NM_030957.4(ADAMTS10):c.*36T>C GRCh37: Chr19:8645741 GRCh38: Chr19:8580857	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 12, 2018)	criteria provided, single submitter
Select item 89386827.	NM_030957.4(ADAMTS10):c.*20G>A GRCh37: Chr19:8645757 GRCh38: Chr19:8580873	ADAMTS10		Weill-Marchesani syndrome, not provided	Benign/Likely benign (May 11, 2021)	criteria provided, multiple submitters, no conflicts
Select item 157321228.	NM_030957.4(ADAMTS10):c.3306C>T (p.Gly1102=) GRCh37: Chr19:8645783 GRCh38: Chr19:8580899	ADAMTS10		not provided	Likely benign (Apr 10, 2022)	criteria provided, single submitter
Select item 51830729.	NM_030957.4(ADAMTS10):c.3303T>G (p.His1101Gln) GRCh37: Chr19:8645786 GRCh38: Chr19:8580902	ADAMTS10	H1101Q, H588Q	not provided, Weill-Marchesani syndrome 1	Benign (Nov 4, 2022)	criteria provided, multiple submitters, no conflicts
Select item 155011230.	NM_030957.4(ADAMTS10):c.3300C>T (p.Cys1100=) GRCh37: Chr19:8645789 GRCh38: Chr19:8580905	ADAMTS10		not provided	Likely benign (Dec 8, 2021)	criteria provided, single submitter
Select item 201763531.	NM_030957.4(ADAMTS10):c.3282del (p.Met1095fs) GRCh37: Chr19:8645807 GRCh38: Chr19:8580923	ADAMTS10	M582fs, M1095fs	not provided	Uncertain significance (Jul 16, 2022)	criteria provided, single submitter
Select item 139200332.	NM_030957.4(ADAMTS10):c.3277C>A (p.Arg1093Ser) GRCh37: Chr19:8645812 GRCh38: Chr19:8580928	ADAMTS10	R580S, R1093S	not provided	Uncertain significance (Oct 3, 2021)	criteria provided, single submitter
Select item 33057633.	NM_030957.4(ADAMTS10):c.3268G>A (p.Ala1090Thr) GRCh37: Chr19:8645821 GRCh38: Chr19:8580937	ADAMTS10	A1090T, A577T	Weill-Marchesani syndrome	Uncertain significance (Jan 12, 2018)	criteria provided, single submitter
Select item 214020934.	NM_030957.4(ADAMTS10):c.3264C>A (p.Ser1088Arg) GRCh37: Chr19:8645825 GRCh38: Chr19:8580941	ADAMTS10	S1088R, S575R	not provided	Uncertain significance (May 21, 2022)	criteria provided, single submitter
Select item 59505035.	NM_030957.4(ADAMTS10):c.3262A>G (p.Ser1088Gly) GRCh37: Chr19:8645827 GRCh38: Chr19:8580943	ADAMTS10	S1088G, S575G	not provided	Uncertain significance (Oct 10, 2022)	criteria provided, multiple submitters, no conflicts
Select item 140888736.	NM_030957.4(ADAMTS10):c.3244C>G (p.Leu1082Val) GRCh37: Chr19:8645845 GRCh38: Chr19:8580961	ADAMTS10	L1082V, L569V	not provided	Uncertain significance (Jun 20, 2022)	criteria provided, single submitter
Select item 139321337.	NM_030957.4(ADAMTS10):c.3221A>G (p.Lys1074Arg) GRCh37: Chr19:8645868 GRCh38: Chr19:8580984	ADAMTS10	K1074R, K561R	not provided	Uncertain significance (Jan 17, 2022)	criteria provided, single submitter
Select item 79937938.	NM_030957.4(ADAMTS10):c.3216G>C (p.Val1072=) GRCh37: Chr19:8645873 GRCh38: Chr19:8580989	ADAMTS10		not provided	Likely benign (Dec 28, 2018)	criteria provided, single submitter
Select item 198965139.	NM_030957.4(ADAMTS10):c.3203-5C>T GRCh37: Chr19:8645891 GRCh38: Chr19:8581007	ADAMTS10		not provided	Benign (Sep 6, 2022)	criteria provided, single submitter
Select item 108570040.	NM_030957.4(ADAMTS10):c.3203-7C>T GRCh37: Chr19:8645893 GRCh38: Chr19:8581009	ADAMTS10		not provided	Likely benign (Oct 20, 2020)	criteria provided, single submitter
Select item 199372141.	NM_030957.4(ADAMTS10):c.3203-8C>G GRCh37: Chr19:8645894 GRCh38: Chr19:8581010	ADAMTS10		not provided	Likely benign (May 12, 2022)	criteria provided, single submitter
Select item 213554042.	NM_030957.4(ADAMTS10):c.3203-10G>C GRCh37: Chr19:8645896 GRCh38: Chr19:8581012	ADAMTS10		not provided	Likely benign (May 8, 2022)	criteria provided, single submitter
Select item 161520243.	NM_030957.4(ADAMTS10):c.3203-13C>T GRCh37: Chr19:8645899 GRCh38: Chr19:8581015	ADAMTS10		not provided	Likely benign (Jul 3, 2022)	criteria provided, single submitter
Select item 195869444.	NM_030957.4(ADAMTS10):c.3203-18_3203-15del GRCh37: Chr19:8645901-8645904 GRCh38: Chr19:8581017-8581020	ADAMTS10		not provided	Likely benign (Jun 29, 2022)	criteria provided, single submitter
Select item 122223345.	NM_030957.4(ADAMTS10):c.3203-129A>G GRCh37: Chr19:8646015 GRCh38: Chr19:8581131	ADAMTS10		not provided	Benign (Sep 21, 2019)	criteria provided, single submitter
Select item 125736246.	NM_030957.4(ADAMTS10):c.3202+252C>T GRCh37: Chr19:8649527 GRCh38: Chr19:8584643	ADAMTS10		not provided	Benign (Mar 21, 2019)	criteria provided, single submitter
Select item 33057747.	NM_030957.4(ADAMTS10):c.3202+13C>T GRCh37: Chr19:8649766 GRCh38: Chr19:8584882	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 13, 2018)	criteria provided, single submitter
Select item 139537148.	NM_030957.4(ADAMTS10):c.3202+9del GRCh37: Chr19:8649770 GRCh38: Chr19:8584886	ADAMTS10		not provided	Uncertain significance (Nov 27, 2021)	criteria provided, single submitter
Select item 8147249.	NM_030957.4(ADAMTS10):c.3193G>A (p.Gly1065Ser) GRCh37: Chr19:8649788 GRCh38: Chr19:8584904	ADAMTS10	G1065S, G552S	Weill-Marchesani syndrome, not specified, not provided	Benign/Likely benign (Oct 28, 2022)	criteria provided, multiple submitters, no conflicts
Select item 198205650.	NM_030957.4(ADAMTS10):c.3182C>A (p.Thr1061Asn) GRCh37: Chr19:8649799 GRCh38: Chr19:8584915	ADAMTS10	T1061N, T548N	not provided	Uncertain significance (Jun 10, 2022)	criteria provided, single submitter
Select item 134751151.	NM_030957.4(ADAMTS10):c.3177C>A (p.Ser1059Arg) GRCh37: Chr19:8649804 GRCh38: Chr19:8584920	ADAMTS10	S546R, S1059R	not provided	Uncertain significance (Oct 27, 2021)	criteria provided, single submitter
Select item 211155452.	NM_030957.4(ADAMTS10):c.3172G>C (p.Asp1058His) GRCh37: Chr19:8649809 GRCh38: Chr19:8584925	ADAMTS10	D1058H, D545H	not provided	Uncertain significance (Mar 14, 2022)	criteria provided, single submitter
Select item 230704953.	NM_030957.4(ADAMTS10):c.3169T>A (p.Cys1057Ser) GRCh37: Chr19:8649812 GRCh38: Chr19:8584928	ADAMTS10	C1057S, C544S	Inborn genetic diseases	Uncertain significance (Aug 16, 2022)	criteria provided, single submitter
Select item 33057854.	NM_030957.4(ADAMTS10):c.3159T>C (p.Cys1053=) GRCh37: Chr19:8649822 GRCh38: Chr19:8584938	ADAMTS10		Weill-Marchesani syndrome	Uncertain significance (Jan 12, 2018)	criteria provided, single submitter
Select item 211746055.	NM_030957.4(ADAMTS10):c.3150G>A (p.Thr1050_Gln1051=) GRCh37: Chr19:8649831 GRCh38: Chr19:8584947	ADAMTS10		not provided	Likely benign (Sep 26, 2022)	criteria provided, single submitter
Select item 204573856.	NM_030957.4(ADAMTS10):c.3149C>T (p.Thr1050Met) GRCh37: Chr19:8649832 GRCh38: Chr19:8584948	ADAMTS10	T1050M, T537M	not provided	Uncertain significance (Feb 25, 2022)	criteria provided, single submitter
Select item 137901357.	NM_030957.4(ADAMTS10):c.3149C>G (p.Thr1050Arg) GRCh37: Chr19:8649832 GRCh38: Chr19:8584948	ADAMTS10	T1050R, T537R	not provided	Uncertain significance (Aug 31, 2021)	criteria provided, single submitter
Select item 156643958.	NM_030957.4(ADAMTS10):c.3141G>T (p.Pro1047=) GRCh37: Chr19:8649840 GRCh38: Chr19:8584956	ADAMTS10		not provided	Likely benign (Nov 12, 2021)	criteria provided, single submitter
Select item 190829059.	NM_030957.4(ADAMTS10):c.3138G>A (p.Arg1046_Pro1047=) GRCh37: Chr19:8649843 GRCh38: Chr19:8584959	ADAMTS10		not provided	Likely benign (Feb 9, 2022)	criteria provided, single submitter
Select item 139992160.	NM_030957.4(ADAMTS10):c.3123C>T (p.Cys1041=) GRCh37: Chr19:8649858 GRCh38: Chr19:8584974	ADAMTS10		not provided	Likely benign (Aug 23, 2022)	criteria provided, single submitter
Select item 197390761.	NM_030957.4(ADAMTS10):c.3120G>A (p.Glu1040_Cys1041=) GRCh37: Chr19:8649861 GRCh38: Chr19:8584977	ADAMTS10		not provided	Likely benign (Apr 18, 2022)	criteria provided, single submitter
Select item 190433562.	NM_030957.4(ADAMTS10):c.3116A>C (p.His1039Pro) GRCh37: Chr19:8649865 GRCh38: Chr19:8584981	ADAMTS10	H1039P, H526P	not provided	Uncertain significance (Aug 19, 2022)	criteria provided, single submitter
Select item 222971363.	NM_030957.4(ADAMTS10):c.3112T>A (p.Ser1038Thr) GRCh37: Chr19:8649869 GRCh38: Chr19:8584985	ADAMTS10	S1038T, S525T	Inborn genetic diseases	Uncertain significance (Mar 25, 2021)	criteria provided, single submitter
Select item 193008964.	NM_030957.4(ADAMTS10):c.3108G>C (p.Gln1036His) GRCh37: Chr19:8649873 GRCh38: Chr19:8584989	ADAMTS10	Q1036H, Q523H	not provided	Uncertain significance (Mar 16, 2022)	criteria provided, single submitter
Select item 33057965.	NM_030957.4(ADAMTS10):c.3102G>A (p.Thr1034=) GRCh37: Chr19:8649879 GRCh38: Chr19:8584995	ADAMTS10		Weill-Marchesani syndrome, not provided	Benign/Likely benign (Nov 4, 2022)	criteria provided, multiple submitters, no conflicts
Select item 142698166.	NM_030957.4(ADAMTS10):c.3097C>T (p.His1033Tyr) GRCh37: Chr19:8649884 GRCh38: Chr19:8585000	ADAMTS10	H1033Y, H520Y	not provided	Uncertain significance (May 5, 2022)	criteria provided, single submitter
Select item 192027067.	NM_030957.4(ADAMTS10):c.3092C>A (p.Thr1031Asn) GRCh37: Chr19:8649889 GRCh38: Chr19:8585005	ADAMTS10	T1031N, T518N	not provided	Uncertain significance (May 25, 2022)	criteria provided, single submitter
Select item 172049168.	NM_030957.4(ADAMTS10):c.3085C>A (p.Arg1029Ser) GRCh37: Chr19:8649896 GRCh38: Chr19:8585012	ADAMTS10	R1029S, R516S	not provided	Uncertain significance (Jul 20, 2022)	criteria provided, single submitter
Select item 197519869.	NM_030957.4(ADAMTS10):c.3084G>A (p.Val1028_Arg1029=) GRCh37: Chr19:8649897 GRCh38: Chr19:8585013	ADAMTS10		not provided	Likely benign (Apr 24, 2022)	criteria provided, single submitter
Select item 111503270.	NM_030957.4(ADAMTS10):c.3081G>A (p.Ser1027=) GRCh37: Chr19:8649900 GRCh38: Chr19:8585016	ADAMTS10		not provided	Likely benign (May 25, 2020)	criteria provided, single submitter
Select item 209028971.	NM_030957.4(ADAMTS10):c.3079T>C (p.Ser1027Pro) GRCh37: Chr19:8649902 GRCh38: Chr19:8585018	ADAMTS10	S1027P, S514P	not provided	Uncertain significance (Apr 15, 2022)	criteria provided, single submitter
Select item 163255972.	NM_030957.4(ADAMTS10):c.3066G>C (p.Gly1022=) GRCh37: Chr19:8649915 GRCh38: Chr19:8585031	ADAMTS10		not provided	Likely benign (Jul 31, 2021)	criteria provided, single submitter
Select item 202042673.	NM_030957.4(ADAMTS10):c.3060C>G (p.Gly1020_Val1021=) GRCh37: Chr19:8649921 GRCh38: Chr19:8585037	ADAMTS10		not provided	Likely benign (Jul 30, 2022)	criteria provided, single submitter
Select item 153552074.	NM_030957.4(ADAMTS10):c.3045C>T (p.Cys1015=) GRCh37: Chr19:8649936 GRCh38: Chr19:8585052	ADAMTS10		not provided	Likely benign (Oct 26, 2021)	criteria provided, single submitter
Select item 157281775.	NM_030957.4(ADAMTS10):c.3043-5C>T GRCh37: Chr19:8649943 GRCh38: Chr19:8585059	ADAMTS10		not provided	Likely benign (Sep 12, 2022)	criteria provided, single submitter
Select item 33058076.	NM_030957.3(ADAMTS10):c.3043-12_3043-6dup GRCh37: Chr19:8649944-8649950 GRCh38: Chr19:8585059-8585060	ADAMTS10		Weill-Marchesani syndrome, not provided	Benign/Likely benign (Nov 4, 2022)	criteria provided, multiple submitters, no conflicts
Select item 33058177.	NM_030957.4(ADAMTS10):c.3043-8C>T GRCh37: Chr19:8649946 GRCh38: Chr19:8585062	ADAMTS10		Weill-Marchesani syndrome, not provided	Conflicting interpretations of pathogenicity (Oct 4, 2022)	criteria provided, conflicting interpretations
Select item 150180178.	NM_030957.4(ADAMTS10):c.3043-10C>A GRCh37: Chr19:8649948 GRCh38: Chr19:8585064	ADAMTS10		not provided	Likely benign (Jul 12, 2022)	criteria provided, single submitter
Select item 165108379.	NM_030957.4(ADAMTS10):c.3042+17del GRCh37: Chr19:8649999 GRCh38: Chr19:8585115	ADAMTS10		not provided	Benign (Apr 22, 2022)	criteria provided, single submitter
Select item 153317880.	NM_030957.4(ADAMTS10):c.3042+16C>A GRCh37: Chr19:8650000 GRCh38: Chr19:8585116	ADAMTS10		not provided	Likely benign (Aug 15, 2021)	criteria provided, single submitter
Select item 144824981.	NM_030957.4(ADAMTS10):c.3017G>A (p.Arg1006His) GRCh37: Chr19:8650041 GRCh38: Chr19:8585157	ADAMTS10	R1006H, R493H	not provided	Uncertain significance (Oct 18, 2022)	criteria provided, single submitter
Select item 101828182.	NM_030957.4(ADAMTS10):c.3011C>T (p.Pro1004Leu) GRCh37: Chr19:8650047 GRCh38: Chr19:8585163	ADAMTS10	P1004L, P491L	Inborn genetic diseases, not provided	Uncertain significance (Jun 27, 2022)	criteria provided, multiple submitters, no conflicts
Select item 161858983.	NM_030957.4(ADAMTS10):c.3006C>T (p.Cys1002=) GRCh37: Chr19:8650052 GRCh38: Chr19:8585168	ADAMTS10		not provided	Likely benign (Aug 31, 2022)	criteria provided, single submitter
Select item 103291784.	NM_030957.4(ADAMTS10):c.3002G>A (p.Arg1001His) GRCh37: Chr19:8650056 GRCh38: Chr19:8585172	ADAMTS10	R1001H, R488H	Weill-Marchesani syndrome 1	Uncertain significance (Aug 30, 2018)	criteria provided, single submitter
Select item 153344885.	NM_030957.4(ADAMTS10):c.2982C>G (p.Thr994=) GRCh37: Chr19:8650076 GRCh38: Chr19:8585192	ADAMTS10		not provided	Benign (Sep 27, 2022)	criteria provided, single submitter
Select item 152373186.	NM_030957.4(ADAMTS10):c.2980A>G (p.Thr994Ala) GRCh37: Chr19:8650078 GRCh38: Chr19:8585194	ADAMTS10	T481A, T994A	not provided	Uncertain significance (Sep 2, 2021)	criteria provided, single submitter
Select item 208024187.	NM_030957.4(ADAMTS10):c.2976G>T (p.Pro992_Ala993=) GRCh37: Chr19:8650082 GRCh38: Chr19:8585198	ADAMTS10		not provided	Likely benign (Jul 27, 2022)	criteria provided, single submitter
Select item 217320188.	NM_030957.4(ADAMTS10):c.2961C>G (p.Pro987_Ala988=) GRCh37: Chr19:8650097 GRCh38: Chr19:8585213	ADAMTS10		not provided	Likely benign (Oct 19, 2022)	criteria provided, single submitter
Select item 159104289.	NM_030957.4(ADAMTS10):c.2961C>T (p.Pro987=) GRCh37: Chr19:8650097 GRCh38: Chr19:8585213	ADAMTS10		not provided	Likely benign (May 17, 2021)	criteria provided, single submitter
Select item 193365190.	NM_030957.4(ADAMTS10):c.2948C>A (p.Ala983Glu) GRCh37: Chr19:8650110 GRCh38: Chr19:8585226	ADAMTS10	A470E, A983E	not provided	Uncertain significance (Mar 20, 2022)	criteria provided, single submitter
Select item 154967091.	NM_030957.4(ADAMTS10):c.2943C>T (p.Pro981=) GRCh37: Chr19:8650115 GRCh38: Chr19:8585231	ADAMTS10		not provided	Likely benign (Oct 8, 2022)	criteria provided, single submitter
Select item 142585092.	NM_030957.4(ADAMTS10):c.2938C>G (p.Leu980Val) GRCh37: Chr19:8650120 GRCh38: Chr19:8585236	ADAMTS10	L467V, L980V	not provided	Uncertain significance (Jul 12, 2022)	criteria provided, single submitter
Select item 199140793.	NM_030957.4(ADAMTS10):c.2925C>T (p.Asp975_His976=) GRCh37: Chr19:8650133 GRCh38: Chr19:8585249	ADAMTS10		not provided	Likely benign (Jul 19, 2022)	criteria provided, single submitter
Select item 193247894.	NM_030957.4(ADAMTS10):c.2918G>C (p.Ser973Thr) GRCh37: Chr19:8650140 GRCh38: Chr19:8585256	ADAMTS10	S973T, S460T	not provided	Uncertain significance (Jul 27, 2022)	criteria provided, single submitter
Select item 199009395.	NM_030957.4(ADAMTS10):c.2908C>T (p.Leu970Phe) GRCh37: Chr19:8650150 GRCh38: Chr19:8585266	ADAMTS10	L457F, L970F	not provided	Uncertain significance (Feb 12, 2022)	criteria provided, single submitter
Select item 190226196.	NM_030957.4(ADAMTS10):c.2895C>A (p.Arg965_His966=) GRCh37: Chr19:8650163 GRCh38: Chr19:8585279	ADAMTS10		not provided	Likely benign (Aug 31, 2022)	criteria provided, single submitter
Select item 217769697.	NM_030957.4(ADAMTS10):c.2886G>C (p.Pro962_Gly963=) GRCh37: Chr19:8650172 GRCh38: Chr19:8585288	ADAMTS10		not provided	Likely benign (Jul 26, 2022)	criteria provided, single submitter
Select item 148705498.	NM_030957.4(ADAMTS10):c.2875A>G (p.Ser959Gly) GRCh37: Chr19:8650183 GRCh38: Chr19:8585299	ADAMTS10	S446G, S959G	not provided	Uncertain significance (Dec 2, 2021)	criteria provided, single submitter
Select item 171598299.	NM_030957.4(ADAMTS10):c.2866T>G (p.Cys956Gly) GRCh37: Chr19:8650192 GRCh38: Chr19:8585308	ADAMTS10	C443G, C956G	not provided	Uncertain significance (Jul 16, 2022)	criteria provided, single submitter
Select item 2420589100.	NM_030957.4(ADAMTS10):c.2866-13C>T GRCh37: Chr19:8650205 GRCh38: Chr19:8585321	ADAMTS10		not provided	Likely benign (Oct 25, 2022)	criteria provided, single submitter

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