Erbb2 Variant Search Result - Rat Genome Database

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766 records found for search term Erbb2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
127288956	CV1147081	single nucleotide variant	NM_004448.4(ERBB2):c.74-5G>T	not provided [RCV001495473]	likely benign	17	39706985	39706985	Human		name
151728495	CV1388645	single nucleotide variant	NM_004448.4(ERBB2):c.73+3G>A	not provided [RCV001966869]	uncertain significance	17	39700314	39700314	Human		name
152051707	CV1597029	single nucleotide variant	NM_004448.4(ERBB2):c.73+9G>A	not provided [RCV002166960]	likely benign	17	39700320	39700320	Human		name
156412841	CV1904617	single nucleotide variant	NM_004448.4(ERBB2):c.74-5G>C	not provided [RCV002587964]	likely benign	17	39706985	39706985	Human		name
597769222	CV3708998	deletion	NM_004448.4(ERBB2):c.2726del	Glioma susceptibility 1 [RCV005020212]	uncertain significance	17	39725706	39725706	Human	4	name
127259431	CV1082969	single nucleotide variant	NM_004448.4(ERBB2):c.226-5C>T	not provided [RCV001419798]	likely benign	17	39708316	39708316	Human		name
150543196	CV1309357	single nucleotide variant	NM_004448.4(ERBB2):c.760-5C>T	not provided [RCV003238429]	uncertain significance	17	39710335	39710335	Human		name
151810642	CV1393425	single nucleotide variant	NM_004448.4(ERBB2):c.225+9C>T	not provided [RCV001953784]	likely benign	17	39707150	39707150	Human		name
151765004	CV1418668	single nucleotide variant	NM_004448.4(ERBB2):c.225+3G>A	not provided [RCV001928955]	uncertain significance	17	39707144	39707144	Human		name
151773381	CV1427785	single nucleotide variant	NM_004448.4(ERBB2):c.575-5C>G	not provided [RCV001915197]	likely benign\|uncertain significance	17	39709808	39709808	Human		name
152030915	CV1580925	single nucleotide variant	NM_004448.4(ERBB2):c.74-12C>T	not provided [RCV002086250]	likely benign	17	39706978	39706978	Human		name
156445086	CV1949142	single nucleotide variant	NM_004448.4(ERBB2):c.226-5C>A	not provided [RCV003116021]	likely benign	17	39708316	39708316	Human		name
402522606	CV2867576	single nucleotide variant	NM_004448.4(ERBB2):c.644-9G>A	not provided [RCV003547875]	likely benign	17	39710077	39710077	Human		name
405167130	CV3018881	single nucleotide variant	NM_004448.4(ERBB2):c.226-7C>T	not provided [RCV003704333]	likely benign	17	39708314	39708314	Human		name
405123939	CV3046590	single nucleotide variant	NM_004448.4(ERBB2):c.643+7C>A	not provided [RCV003724125]	likely benign	17	39709888	39709888	Human		name
405133333	CV3047532	single nucleotide variant	NM_004448.4(ERBB2):c.902-7T>C	not provided [RCV003725024]	likely benign	17	39711921	39711921	Human		name
405217356	CV3048824	single nucleotide variant	NM_004448.4(ERBB2):c.439+2T>C	not provided [RCV003732825]	uncertain significance	17	39708536	39708536	Human		name
405144333	CV3056269	single nucleotide variant	NM_004448.4(ERBB2):c.574+1G>C	not provided [RCV003725921]	uncertain significance	17	39709453	39709453	Human		name
405180872	CV3057232	single nucleotide variant	NM_004448.4(ERBB2):c.439+4G>A	not provided [RCV003728760]	uncertain significance	17	39708538	39708538	Human		name
405225277	CV3058233	deletion	NM_004448.4(ERBB2):c.73+17del	not provided [RCV003733858]	benign	17	39700325	39700325	Human		name
405223684	CV3061399	single nucleotide variant	NM_004448.4(ERBB2):c.74-12C>G	not provided [RCV003733700]	likely benign	17	39706978	39706978	Human		name
597834916	CV3739581	single nucleotide variant	NM_004448.4(ERBB2):c.440-5C>T	not provided [RCV005063800]	likely benign	17	39709313	39709313	Human		name
597846307	CV3827950	single nucleotide variant	NM_004448.4(ERBB2):c.902-6C>T	not provided [RCV005173025]	likely benign	17	39711922	39711922	Human		name
597926995	CV3836864	duplication	NM_004448.4(ERBB2):c.760-9dup	not provided [RCV005185215]	likely benign	17	39710330	39710331	Human		name
597957693	CV3848926	single nucleotide variant	NM_004448.4(ERBB2):c.74-16T>C	not provided [RCV005191927]	likely benign	17	39706974	39706974	Human		name
15119156	CV745057	single nucleotide variant	NM_004448.4(ERBB2):c.901+7G>T	not provided [RCV000895673]	benign	17	39710488	39710488	Human		name
126922394	CV1050223	single nucleotide variant	NM_004448.4(ERBB2):c.1738-7C>A	not provided [RCV001364624]	likely benign\|uncertain significance	17	39717313	39717313	Human		name
126919193	CV1050225	single nucleotide variant	NM_004448.4(ERBB2):c.2493+5G>A	not provided [RCV001373092]	uncertain significance	17	39724916	39724916	Human		name
127279174	CV1104771	single nucleotide variant	NM_004448.4(ERBB2):c.2307+7C>T	not provided [RCV001445571]	likely benign	17	39724017	39724017	Human		name
127251630	CV1104774	single nucleotide variant	NM_004448.4(ERBB2):c.3160-8G>A	not provided [RCV001425645]	likely benign	17	39727287	39727287	Human		name
127291097	CV1126182	single nucleotide variant	NM_004448.4(ERBB2):c.760-10G>T	not provided [RCV001475969]	likely benign	17	39710330	39710330	Human		name
127287156	CV1147085	single nucleotide variant	NM_004448.4(ERBB2):c.1947-8G>A	not provided [RCV001494774]	likely benign	17	39723311	39723311	Human		name
8688906	CV136693	single nucleotide variant	NM_004448.4(ERBB2):c.2494-3C>T	Familial cancer of breast [RCV000119345]\|not provided [RCV002514597]	uncertain significance\|not provided	17	39725046	39725046	Human	1	name
151885051	CV1425253	single nucleotide variant	NM_004448.4(ERBB2):c.1021+5C>G	not provided [RCV001887275]	uncertain significance	17	39712052	39712052	Human		name
151848736	CV1510572	single nucleotide variant	NM_004448.4(ERBB2):c.2493+6C>T	not provided [RCV001957689]	uncertain significance	17	39724917	39724917	Human		name
152025779	CV1527984	single nucleotide variant	NM_004448.4(ERBB2):c.574+15T>A	not provided [RCV002084578]	likely benign	17	39709467	39709467	Human		name
152111852	CV1539136	single nucleotide variant	NM_004448.4(ERBB2):c.225+10G>A	not provided [RCV002080361]	likely benign	17	39707151	39707151	Human		name
152176287	CV1541383	single nucleotide variant	NM_004448.4(ERBB2):c.439+13G>A	not provided [RCV002164432]	likely benign	17	39708547	39708547	Human		name
152158100	CV1542167	single nucleotide variant	NM_004448.4(ERBB2):c.902-17G>A	not provided [RCV002202955]	likely benign	17	39711911	39711911	Human		name
152081929	CV1548352	single nucleotide variant	NM_004448.4(ERBB2):c.3160-4C>T	not provided [RCV002076485]	likely benign	17	39727291	39727291	Human		name
152079195	CV1549929	single nucleotide variant	NM_004448.4(ERBB2):c.1738-4C>G	not provided [RCV002192811]	likely benign	17	39717316	39717316	Human		name
152127855	CV1572152	single nucleotide variant	NM_004448.4(ERBB2):c.1738-4C>A	not provided [RCV002217655]	likely benign	17	39717316	39717316	Human		name
152114551	CV1573682	single nucleotide variant	NM_004448.4(ERBB2):c.1149-4C>T	not provided [RCV002215951]	likely benign	17	39715282	39715282	Human		name
152088942	CV1580539	deletion	NM_004448.4(ERBB2):c.2209-9del	not provided [RCV002093902]	likely benign	17	39723901	39723901	Human		name
152156256	CV1589488	single nucleotide variant	NM_004448.4(ERBB2):c.1738-9C>T	not provided [RCV002122474]	likely benign	17	39717311	39717311	Human		name
152149089	CV1593083	single nucleotide variant	NM_004448.4(ERBB2):c.1149-8C>G	not provided [RCV002101943]	likely benign	17	39715278	39715278	Human		name
152117873	CV1601080	single nucleotide variant	NM_004448.4(ERBB2):c.2307+9C>T	not provided [RCV002097743]	likely benign	17	39724019	39724019	Human		name
152095870	CV1627810	duplication	NM_004448.4(ERBB2):c.1738-3dup	not provided [RCV002194909]	benign	17	39717309	39717310	Human		name
152146936	CV1649647	single nucleotide variant	NM_004448.4(ERBB2):c.1899-9C>T	not provided [RCV002121195]	likely benign	17	39719778	39719778	Human		name
152110749	CV1651062	single nucleotide variant	NM_004448.4(ERBB2):c.2873-5C>T	not provided [RCV002134453]	likely benign	17	39726557	39726557	Human		name
156280239	CV1877023	duplication	NM_004448.4(ERBB2):c.1149-6dup	not provided [RCV003061037]	benign	17	39715276	39715277	Human		name
156318119	CV1900057	single nucleotide variant	NM_004448.4(ERBB2):c.2650-9C>T	not provided [RCV003088838]	likely benign	17	39725318	39725318	Human		name
156361982	CV1900618	single nucleotide variant	NM_004448.4(ERBB2):c.901+10A>G	not provided [RCV002581788]	likely benign	17	39710491	39710491	Human		name
156167719	CV1907832	single nucleotide variant	NM_004448.4(ERBB2):c.1947-9C>T	not provided [RCV003083127]	likely benign	17	39723310	39723310	Human		name
156300900	CV1916087	single nucleotide variant	NM_004448.4(ERBB2):c.2085+9G>A	not provided [RCV002599166]	likely benign	17	39723466	39723466	Human		name
156368474	CV1922551	single nucleotide variant	NM_004448.4(ERBB2):c.2086-6C>A	not provided [RCV002633191]	likely benign	17	39723532	39723532	Human		name
156441325	CV1945572	single nucleotide variant	NM_004448.4(ERBB2):c.226-11C>T	not provided [RCV003111377]	likely benign	17	39708310	39708310	Human		name
156441042	CV1949329	single nucleotide variant	NM_004448.4(ERBB2):c.902-12T>C	not provided [RCV003111090]	likely benign	17	39711916	39711916	Human		name
156446054	CV1951081	single nucleotide variant	NM_004448.4(ERBB2):c.439+16A>G	not provided [RCV003117017]	benign	17	39708550	39708550	Human		name
156446080	CV1951105	single nucleotide variant	NM_004448.4(ERBB2):c.1738-4C>T	not provided [RCV003117043]	likely benign	17	39717316	39717316	Human		name
156286277	CV2001741	single nucleotide variant	NM_004448.4(ERBB2):c.1738-5C>A	not provided [RCV002647021]	likely benign	17	39717315	39717315	Human		name
156354618	CV2012124	single nucleotide variant	NM_004448.4(ERBB2):c.760-13C>T	not provided [RCV002720433]	likely benign	17	39710327	39710327	Human		name
156109817	CV2038710	single nucleotide variant	NM_004448.4(ERBB2):c.1947-7C>T	not provided [RCV002761646]	likely benign	17	39723312	39723312	Human		name
156022754	CV2043268	single nucleotide variant	NM_004448.4(ERBB2):c.440-10C>T	not provided [RCV002780733]	uncertain significance	17	39709308	39709308	Human		name
156127392	CV2046949	single nucleotide variant	NM_004448.4(ERBB2):c.2209-6G>A	not provided [RCV002800476]	likely benign	17	39723906	39723906	Human		name
156133394	CV2047907	single nucleotide variant	NM_004448.4(ERBB2):c.1738-5C>T	not provided [RCV002800695]	likely benign	17	39717315	39717315	Human		name
155907853	CV2052428	single nucleotide variant	NM_004448.4(ERBB2):c.1313+9T>A	not provided [RCV002837489]	likely benign	17	39715545	39715545	Human		name
405188640	CV2917888	single nucleotide variant	NM_004448.4(ERBB2):c.1313+8C>T	not provided [RCV003564674]	likely benign	17	39715544	39715544	Human		name
402516376	CV2993232	single nucleotide variant	NM_004448.4(ERBB2):c.440-12C>T	not provided [RCV003716024]	uncertain significance	17	39709306	39709306	Human		name
405000033	CV3008970	single nucleotide variant	NM_004448.4(ERBB2):c.1513+3A>C	not provided [RCV003693002]	uncertain significance	17	39715942	39715942	Human		name
405184099	CV3040180	single nucleotide variant	NM_004448.4(ERBB2):c.1148+9G>A	not provided [RCV003705842]	likely benign	17	39712457	39712457	Human		name
405242512	CV3042857	deletion	NM_004448.4(ERBB2):c.1738-3del	not provided [RCV003719511]	benign	17	39717310	39717310	Human		name
405085224	CV3043805	single nucleotide variant	NM_004448.4(ERBB2):c.2970+5T>C	not provided [RCV003717424]	uncertain significance	17	39726664	39726664	Human		name
405177129	CV3049529	single nucleotide variant	NM_004448.4(ERBB2):c.2725+9T>C	not provided [RCV003728440]	likely benign	17	39725411	39725411	Human		name
405132513	CV3051295	single nucleotide variant	NM_004448.4(ERBB2):c.1223-8G>A	not provided [RCV003724953]	likely benign	17	39715438	39715438	Human		name
405245504	CV3051564	single nucleotide variant	NM_004448.4(ERBB2):c.1647-5C>T	not provided [RCV003720321]	likely benign	17	39716510	39716510	Human		name
405129024	CV3054458	single nucleotide variant	NM_004448.4(ERBB2):c.2494-6T>C	not provided [RCV003724655]	likely benign	17	39725043	39725043	Human		name
405225135	CV3058206	single nucleotide variant	NM_004448.4(ERBB2):c.759+13G>T	not provided [RCV003733847]	likely benign	17	39710214	39710214	Human		name
405224835	CV3058248	single nucleotide variant	NM_004448.4(ERBB2):c.225+14G>C	not provided [RCV003733864]	likely benign	17	39707155	39707155	Human		name
405211746	CV3063060	deletion	NM_004448.4(ERBB2):c.1021+9del	not provided [RCV003732110]	likely benign	17	39712056	39712056	Human		name
405089631	CV3118427	single nucleotide variant	NM_004448.4(ERBB2):c.2085+8G>C	not provided [RCV003811069]	likely benign	17	39723465	39723465	Human		name
404992794	CV3132412	single nucleotide variant	NM_004448.4(ERBB2):c.3412+7A>T	not provided [RCV003827351]	likely benign	17	39727554	39727554	Human		name
402468173	CV3174270	single nucleotide variant	NM_004448.4(ERBB2):c.1737+8G>C	not provided [RCV003873553]	likely benign	17	39716613	39716613	Human		name
597769189	CV3708993	single nucleotide variant	NM_004448.4(ERBB2):c.1314-3T>C	Glioma susceptibility 1 [RCV005020206]	uncertain significance	17	39715737	39715737	Human	4	name
597769212	CV3708996	single nucleotide variant	NM_004448.4(ERBB2):c.2085+7C>T	Glioma susceptibility 1 [RCV005020210]	uncertain significance	17	39723464	39723464	Human	4	name
597836424	CV3757684	single nucleotide variant	NM_004448.4(ERBB2):c.3159+7G>C	not provided [RCV005085698]	likely benign	17	39727010	39727010	Human		name
597926541	CV3819726	single nucleotide variant	NM_004448.4(ERBB2):c.574+14C>A	not provided [RCV005156426]	likely benign	17	39709466	39709466	Human		name
597967270	CV3824194	single nucleotide variant	NM_004448.4(ERBB2):c.2970+6G>T	not provided [RCV005165417]	uncertain significance	17	39726665	39726665	Human		name
597950715	CV3847032	deletion	NM_004448.4(ERBB2):c.2085+7del	not provided [RCV005190203]	likely benign	17	39723464	39723464	Human		name
15153378	CV744965	single nucleotide variant	NM_004448.4(ERBB2):c.2650-5C>G	not provided [RCV000901749]	benign	17	39725322	39725322	Human		name
15156665	CV760413	single nucleotide variant	NM_004448.4(ERBB2):c.1738-5C>G	not provided [RCV000924713]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	17	39717315	39717315	Human		name
26915868	CV852197	single nucleotide variant	NM_004448.4(ERBB2):c.2872+4C>T	not provided [RCV001039517]	uncertain significance	17	39725857	39725857	Human		name
38494943	CV960884	single nucleotide variant	NM_004448.4(ERBB2):c.3159+1G>C	not provided [RCV001241655]	uncertain significance	17	39727004	39727004	Human		name
127260684	CV1082971	single nucleotide variant	NM_004448.4(ERBB2):c.1646+10G>A	not provided [RCV001420098]	likely benign	17	39716443	39716443	Human		name
127273939	CV1082973	single nucleotide variant	NM_004448.4(ERBB2):c.1898+10A>G	not provided [RCV001406200]	likely benign	17	39717490	39717490	Human		name
8686661	CV139259	single nucleotide variant	NM_004448.4(ERBB2):c.1021+19C>T	not provided [RCV002055373]\|not specified [RCV000122380]	benign\|not provided	17	39712066	39712066	Human		name
8686662	CV139260	single nucleotide variant	NM_004448.4(ERBB2):c.1021+31C>T	not specified [RCV000122381]	not provided	17	39712078	39712078	Human		name
8686663	CV139261	single nucleotide variant	NM_004448.4(ERBB2):c.1021+48C>T	not specified [RCV000122382]	not provided	17	39712095	39712095	Human		name
151730409	CV1441239	single nucleotide variant	NM_004448.4(ERBB2):c.1737+13C>T	not provided [RCV001945987]	likely benign\|uncertain significance	17	39716618	39716618	Human		name
151856426	CV1464694	single nucleotide variant	NM_004448.4(ERBB2):c.1514-11C>G	not provided [RCV001958647]	likely benign	17	39716290	39716290	Human		name
152027797	CV1529584	single nucleotide variant	NM_004448.4(ERBB2):c.3160-15C>T	not provided [RCV002185623]	likely benign	17	39727280	39727280	Human		name
152069023	CV1535283	single nucleotide variant	NM_004448.4(ERBB2):c.1513+13G>A	not provided [RCV002091331]	likely benign	17	39715952	39715952	Human		name
152069414	CV1535397	single nucleotide variant	NM_004448.4(ERBB2):c.1223-14C>A	not provided [RCV002091380]	likely benign	17	39715432	39715432	Human		name
152143325	CV1538382	single nucleotide variant	NM_004448.4(ERBB2):c.2308-14A>G	not provided [RCV002219666]	likely benign	17	39724712	39724712	Human		name
152089393	CV1541574	single nucleotide variant	NM_004448.4(ERBB2):c.1737+14G>A	not provided [RCV002171627]	likely benign	17	39716619	39716619	Human		name
152158839	CV1544286	single nucleotide variant	NM_004448.4(ERBB2):c.3159+13G>A	not provided [RCV002122835]	benign	17	39727016	39727016	Human		name
152109038	CV1556404	single nucleotide variant	NM_004448.4(ERBB2):c.1947-14G>T	not provided [RCV002096590]	likely benign	17	39723305	39723305	Human		name
152079076	CV1557833	single nucleotide variant	NM_004448.4(ERBB2):c.1737+15G>A	not provided [RCV002170306]	likely benign	17	39716620	39716620	Human		name
152089247	CV1580613	single nucleotide variant	NM_004448.4(ERBB2):c.2209-12C>T	not provided [RCV002093940]	likely benign	17	39723900	39723900	Human		name
152089437	CV1580660	single nucleotide variant	NM_004448.4(ERBB2):c.1223-13C>T	not provided [RCV002093964]	likely benign	17	39715433	39715433	Human		name
152119363	CV1593635	single nucleotide variant	NM_004448.4(ERBB2):c.2086-11C>G	not provided [RCV002097937]	benign	17	39723527	39723527	Human		name
152118181	CV1594870	duplication	NM_004448.4(ERBB2):c.1899-10dup	not provided [RCV002197683]	likely benign	17	39719774	39719775	Human		name
152136498	CV1595151	single nucleotide variant	NM_004448.4(ERBB2):c.3413-18C>T	not provided [RCV002200013]	likely benign	17	39727671	39727671	Human		name
152133408	CV1607380	single nucleotide variant	NM_004448.4(ERBB2):c.2873-17C>A	not provided [RCV002119373]	likely benign	17	39726545	39726545	Human		name
152098770	CV1611774	single nucleotide variant	NM_004448.4(ERBB2):c.2493+15T>C	not provided [RCV002172820]	likely benign	17	39724926	39724926	Human		name
152122552	CV1613418	single nucleotide variant	NM_004448.4(ERBB2):c.1314-15A>C	not provided [RCV002154445]	likely benign	17	39715725	39715725	Human		name
152140220	CV1625102	single nucleotide variant	NM_004448.4(ERBB2):c.2873-15T>A	not provided [RCV002219270]	likely benign	17	39726547	39726547	Human		name
152038399	CV1625177	single nucleotide variant	NM_004448.4(ERBB2):c.2494-15T>C	not provided [RCV002205967]	likely benign	17	39725034	39725034	Human		name
152140961	CV1625224	single nucleotide variant	NM_004448.4(ERBB2):c.1946+12C>T	not provided [RCV002219365]	likely benign	17	39719846	39719846	Human		name
152166873	CV1632680	deletion	NM_004448.4(ERBB2):c.1314-16del	not provided [RCV002182021]	likely benign	17	39715722	39715722	Human		name
152080367	CV1663628	single nucleotide variant	NM_004448.4(ERBB2):c.1149-14C>G	not provided [RCV002149229]	likely benign	17	39715272	39715272	Human		name
156403526	CV1885820	single nucleotide variant	NM_004448.4(ERBB2):c.1738-10C>T	not provided [RCV003069494]	likely benign	17	39717310	39717310	Human		name
156377994	CV1906779	single nucleotide variant	NM_004448.4(ERBB2):c.2308-10T>C	not provided [RCV003093033]	likely benign	17	39724716	39724716	Human		name
156443221	CV1943101	single nucleotide variant	NM_004448.4(ERBB2):c.2872+16G>C	not provided [RCV003113596]	likely benign	17	39725869	39725869	Human		name
156440921	CV1949200	single nucleotide variant	NM_004448.4(ERBB2):c.1222+20C>T	not provided [RCV003110965]	likely benign	17	39715379	39715379	Human		name
156441009	CV1949292	single nucleotide variant	NM_004448.4(ERBB2):c.3159+12C>T	not provided [RCV003111056]	likely benign	17	39727015	39727015	Human		name
156441022	CV1949306	single nucleotide variant	NM_004448.4(ERBB2):c.2308-16G>A	not provided [RCV003111069]	likely benign	17	39724710	39724710	Human		name
156445959	CV1950984	single nucleotide variant	NM_004448.4(ERBB2):c.3159+12C>G	not provided [RCV003116922]	likely benign	17	39727015	39727015	Human		name
156445969	CV1950993	single nucleotide variant	NM_004448.4(ERBB2):c.1021+15C>T	not provided [RCV003116932]	likely benign	17	39712062	39712062	Human		name
156446046	CV1951073	single nucleotide variant	NM_004448.4(ERBB2):c.1513+17A>G	Glioma susceptibility 1 [RCV005021808]\|not provided [RCV003117009]	likely benign\|uncertain significance	17	39715956	39715956	Human	4	name
156443778	CV1952084	deletion	NM_004448.4(ERBB2):c.2971-10del	not provided [RCV003114158]	likely benign	17	39726804	39726804	Human		name
156411517	CV1973447	single nucleotide variant	NM_004448.4(ERBB2):c.2493+19T>C	not provided [RCV002608275]	likely benign	17	39724930	39724930	Human		name
156142056	CV2082365	single nucleotide variant	NM_004448.4(ERBB2):c.1513+18G>T	not provided [RCV002872018]	likely benign	17	39715957	39715957	Human		name
402474619	CV2863541	single nucleotide variant	NM_004448.4(ERBB2):c.1513+18G>C	not provided [RCV003543162]	likely benign	17	39715957	39715957	Human		name
402487518	CV2941446	duplication	NM_004448.4(ERBB2):c.1737+12dup	not provided [RCV003660223]	likely benign	17	39716615	39716616	Human		name
405140469	CV2961845	single nucleotide variant	NM_004448.4(ERBB2):c.2971-17C>T	not provided [RCV003673108]	likely benign	17	39726798	39726798	Human		name
405243100	CV3043926	duplication	NM_004448.4(ERBB2):c.2725+15dup	not provided [RCV003719655]	benign	17	39725411	39725412	Human		name
405225558	CV3058477	single nucleotide variant	NM_004448.4(ERBB2):c.2726-11C>T	not provided [RCV003733980]	likely benign	17	39725696	39725696	Human		name
405223332	CV3061276	single nucleotide variant	NM_004448.4(ERBB2):c.1314-19G>A	not provided [RCV003733649]	likely benign	17	39715721	39715721	Human		name
405224108	CV3061298	single nucleotide variant	NM_004448.4(ERBB2):c.2970+18C>T	not provided [RCV003733664]	likely benign	17	39726677	39726677	Human		name
405223455	CV3061301	single nucleotide variant	NM_004448.4(ERBB2):c.1313+17A>C	not provided [RCV003733667]	likely benign	17	39715553	39715553	Human		name
405223496	CV3061314	single nucleotide variant	NM_004448.4(ERBB2):c.1313+13A>C	not provided [RCV003733673]	likely benign	17	39715549	39715549	Human		name
405223545	CV3061345	single nucleotide variant	NM_004448.4(ERBB2):c.2650-15C>G	not provided [RCV003733681]	likely benign	17	39725312	39725312	Human		name
405163691	CV3125160	single nucleotide variant	NM_004448.4(ERBB2):c.2649+13A>C	not provided [RCV003818432]	likely benign	17	39725217	39725217	Human		name
597948957	CV3848786	single nucleotide variant	NM_004448.4(ERBB2):c.2307+16C>T	not provided [RCV005189723]	likely benign	17	39724026	39724026	Human		name
597949452	CV3848793	single nucleotide variant	NM_004448.4(ERBB2):c.1314-13C>T	not provided [RCV005189730]	likely benign	17	39715727	39715727	Human		name
597948989	CV3848795	single nucleotide variant	NM_004448.4(ERBB2):c.1898+11C>T	not provided [RCV005189732]	likely benign	17	39717491	39717491	Human		name
597948614	CV3852537	single nucleotide variant	NM_004448.4(ERBB2):c.1222+19T>A	not provided [RCV005189615]	likely benign	17	39715378	39715378	Human		name
597948622	CV3852538	single nucleotide variant	NM_004448.4(ERBB2):c.1647-19C>T	not provided [RCV005189616]	likely benign	17	39716496	39716496	Human		name
597898197	CV3854474	single nucleotide variant	NM_004448.4(ERBB2):c.2650-10G>A	not provided [RCV005201581]	likely benign	17	39725317	39725317	Human		name
152039377	CV1555322	single nucleotide variant	NM_004448.4(ERBB2):c.15C>G (p.Ala5=)	not provided [RCV002107508]	likely benign	17	39700253	39700253	Human		name
127272847	CV1104764	single nucleotide variant	NM_004448.4(ERBB2):c.81C>T (p.Thr27=)	not provided [RCV001442345]	likely benign	17	39706997	39706997	Human		name
151812721	CV1349760	single nucleotide variant	NM_004448.4(ERBB2):c.54C>A (p.Pro18=)	not provided [RCV001974935]	likely benign\|uncertain significance	17	39700292	39700292	Human		name
151795057	CV1506306	single nucleotide variant	NM_004448.4(ERBB2):c.7C>G (p.Leu3Val)	not provided [RCV001917179]	uncertain significance	17	39700245	39700245	Human		name
152175052	CV1536338	single nucleotide variant	NM_004448.4(ERBB2):c.51C>T (p.Pro17=)	not provided [RCV002163355]	likely benign	17	39700289	39700289	Human		name
152165584	CV1543814	single nucleotide variant	NM_004448.4(ERBB2):c.78C>T (p.Cys26=)	not provided [RCV002124045]	likely benign	17	39706994	39706994	Human		name
152108942	CV1604082	single nucleotide variant	NM_004448.4(ERBB2):c.51C>A (p.Pro17=)	not provided [RCV002079982]	benign	17	39700289	39700289	Human		name
152165589	CV1611393	single nucleotide variant	NM_004448.4(ERBB2):c.39C>T (p.Leu13=)	not provided [RCV002141749]	likely benign	17	39700277	39700277	Human		name
156029241	CV1903216	single nucleotide variant	NM_004448.4(ERBB2):c.69C>T (p.Thr23=)	not provided [RCV003100573]	likely benign	17	39700307	39700307	Human		name
405245424	CV3054950	single nucleotide variant	NM_004448.4(ERBB2):c.90C>T (p.Asp30=)	not provided [RCV003720202]	likely benign	17	39707006	39707006	Human		name
597953178	CV3798919	single nucleotide variant	NM_004448.4(ERBB2):c.63G>A (p.Ala21=)	not provided [RCV005136493]	likely benign	17	39700301	39700301	Human		name
597871250	CV3849293	single nucleotide variant	NM_004448.4(ERBB2):c.36C>T (p.Leu12=)	not provided [RCV005197474]	likely benign	17	39700274	39700274	Human		name
15119125	CV715414	single nucleotide variant	NM_004448.4(ERBB2):c.99G>A (p.Leu33=)	not provided [RCV000962495]	benign	17	39707015	39707015	Human		name
127273234	CV1104765	single nucleotide variant	NM_004448.4(ERBB2):c.111C>A (p.Ala37=)	not provided [RCV001442461]	likely benign	17	39707027	39707027	Human		name
152162984	CV1537522	single nucleotide variant	NM_004448.4(ERBB2):c.192C>T (p.Tyr64=)	not provided [RCV002159976]	likely benign	17	39707108	39707108	Human		name
152060695	CV1540823	single nucleotide variant	NM_004448.4(ERBB2):c.288G>A (p.Leu96=)	not provided [RCV002190488]	likely benign	17	39708383	39708383	Human		name
152055159	CV1590843	single nucleotide variant	NM_004448.4(ERBB2):c.105C>T (p.Leu35=)	not provided [RCV002109447]	likely benign	17	39707021	39707021	Human		name
152057139	CV1635148	single nucleotide variant	NM_004448.4(ERBB2):c.201C>G (p.Thr67=)	not provided [RCV002089842]	likely benign	17	39707117	39707117	Human		name
156110406	CV1903874	single nucleotide variant	NM_004448.4(ERBB2):c.117C>T (p.Pro39=)	not provided [RCV003080946]	likely benign	17	39707033	39707033	Human		name
405131715	CV3054419	single nucleotide variant	NM_004448.4(ERBB2):c.282C>A (p.Val94=)	not provided [RCV003724630]	likely benign	17	39708377	39708377	Human		name
405740316	CV3259339	single nucleotide variant	NM_004448.4(ERBB2):c.10G>T (p.Ala4Ser)	not specified [RCV004380477]	uncertain significance	17	39700248	39700248	Human		name
15192477	CV740710	single nucleotide variant	NM_004448.4(ERBB2):c.258C>T (p.Ile86=)	not provided [RCV000910553]	likely benign	17	39708353	39708353	Human		name
127270122	CV1104766	single nucleotide variant	NM_004448.4(ERBB2):c.717G>A (p.Gln239=)	not provided [RCV001441338]	likely benign	17	39710159	39710159	Human		name
127266912	CV1104767	single nucleotide variant	NM_004448.4(ERBB2):c.816C>A (p.Val272=)	not provided [RCV001429503]	likely benign	17	39710396	39710396	Human		name
127314851	CV1126181	single nucleotide variant	NM_004448.4(ERBB2):c.675C>G (p.Ala225=)	not provided [RCV001465080]	likely benign	17	39710117	39710117	Human		name
127293597	CV1126183	single nucleotide variant	NM_004448.4(ERBB2):c.768C>T (p.Leu256=)	not provided [RCV001452037]	likely benign	17	39710348	39710348	Human		name
127335727	CV1147082	single nucleotide variant	NM_004448.4(ERBB2):c.498G>C (p.Thr166=)	not provided [RCV001491690]	likely benign	17	39709376	39709376	Human		name
127337986	CV1147083	single nucleotide variant	NM_004448.4(ERBB2):c.735G>C (p.Thr245=)	not provided [RCV001493347]	likely benign	17	39710177	39710177	Human		name
8687356	CV137806	single nucleotide variant	NM_004448.4(ERBB2):c.43C>T (p.Leu15Phe)	not provided [RCV001439480]\|not specified [RCV000120736]	likely benign\|not provided	17	39700281	39700281	Human		name
8687365	CV137815	single nucleotide variant	NM_004448.4(ERBB2):c.93G>T (p.Met31Ile)	not provided [RCV001464145]\|not specified [RCV000120747]	likely benign\|not provided	17	39707009	39707009	Human		name
151877510	CV1382402	single nucleotide variant	NM_004448.4(ERBB2):c.74T>C (p.Val25Ala)	Glioma susceptibility 1 [RCV005017041]\|not provided [RCV002019717]	uncertain significance	17	39706990	39706990	Human	4	name
151739811	CV1386385	single nucleotide variant	NM_004448.4(ERBB2):c.79A>C (p.Thr27Pro)	not provided [RCV001893157]	uncertain significance	17	39706995	39706995	Human		name
151846215	CV1386389	single nucleotide variant	NM_004448.4(ERBB2):c.59C>T (p.Ala20Val)	not provided [RCV001881976]	uncertain significance	17	39700297	39700297	Human		name
151762817	CV1499240	single nucleotide variant	NM_004448.4(ERBB2):c.65G>A (p.Ser22Asn)	not provided [RCV001863298]	uncertain significance	17	39700303	39700303	Human		name
152135775	CV1528364	single nucleotide variant	NM_004448.4(ERBB2):c.522C>T (p.His174=)	not provided [RCV002100096]	likely benign	17	39709400	39709400	Human		name
152063511	CV1535623	single nucleotide variant	NM_004448.4(ERBB2):c.939C>T (p.Leu313=)	not provided [RCV002168301]	likely benign	17	39711965	39711965	Human		name
152135152	CV1549951	single nucleotide variant	NM_004448.4(ERBB2):c.366G>A (p.Pro122=)	not provided [RCV002199844]	likely benign	17	39708461	39708461	Human		name
152134970	CV1564903	single nucleotide variant	NM_004448.4(ERBB2):c.876C>T (p.Gly292=)	not provided [RCV002199825]	likely benign	17	39710456	39710456	Human		name
152118365	CV1594899	single nucleotide variant	NM_004448.4(ERBB2):c.705C>T (p.Cys235=)	not provided [RCV002197706]	likely benign	17	39710147	39710147	Human		name
152115304	CV1641055	single nucleotide variant	NM_004448.4(ERBB2):c.855C>T (p.Pro285=)	not provided [RCV002117101]	likely benign	17	39710435	39710435	Human		name
152153894	CV1643503	single nucleotide variant	NM_004448.4(ERBB2):c.498G>A (p.Thr166=)	not provided [RCV002122147]	likely benign	17	39709376	39709376	Human		name
152101370	CV1645794	single nucleotide variant	NM_004448.4(ERBB2):c.726C>T (p.Ala242=)	not provided [RCV002173148]	likely benign	17	39710168	39710168	Human		name
152048488	CV1654190	single nucleotide variant	NM_004448.4(ERBB2):c.870A>G (p.Thr290=)	not provided [RCV002088838]	likely benign	17	39710450	39710450	Human		name
152070011	CV1660816	single nucleotide variant	NM_004448.4(ERBB2):c.999G>A (p.Lys333=)	not provided [RCV002129489]	likely benign	17	39712025	39712025	Human		name
156414161	CV1915767	single nucleotide variant	NM_004448.4(ERBB2):c.921C>T (p.Asp307=)	not provided [RCV002588446]	likely benign	17	39711947	39711947	Human		name
156026564	CV1918839	single nucleotide variant	NM_004448.4(ERBB2):c.474C>T (p.Asn158=)	not provided [RCV002636972]	likely benign	17	39709352	39709352	Human		name
156410167	CV1932189	single nucleotide variant	NM_004448.4(ERBB2):c.744G>A (p.Lys248=)	not provided [RCV002607781]	likely benign	17	39710186	39710186	Human		name
156440187	CV1946549	single nucleotide variant	NM_004448.4(ERBB2):c.41C>T (p.Ala14Val)	not provided [RCV003110218]	uncertain significance	17	39700279	39700279	Human		name
156211715	CV2018898	single nucleotide variant	NM_004448.4(ERBB2):c.738C>T (p.Gly246=)	not provided [RCV002700652]	likely benign	17	39710180	39710180	Human		name
156115682	CV2084928	single nucleotide variant	NM_004448.4(ERBB2):c.402A>G (p.Pro134=)	not provided [RCV002889361]	likely benign	17	39708497	39708497	Human		name
155994900	CV2122513	single nucleotide variant	NM_004448.4(ERBB2):c.340C>T (p.Leu114=)	not provided [RCV002974903]	likely benign	17	39708435	39708435	Human		name
155902302	CV2127023	single nucleotide variant	NM_004448.4(ERBB2):c.792T>C (p.Cys264=)	not provided [RCV002967497]	likely benign	17	39710372	39710372	Human		name
156306415	CV2129797	single nucleotide variant	NM_004448.4(ERBB2):c.643C>T (p.Leu215=)	not provided [RCV002962386]	likely benign	17	39709881	39709881	Human		name
405124611	CV3043393	single nucleotide variant	NM_004448.4(ERBB2):c.864G>A (p.Arg288=)	not provided [RCV003724247]	likely benign	17	39710444	39710444	Human		name
405252903	CV3044099	single nucleotide variant	NM_004448.4(ERBB2):c.91A>T (p.Met31Leu)	not provided [RCV003722352]	uncertain significance	17	39707007	39707007	Human		name
405177331	CV3049611	single nucleotide variant	NM_004448.4(ERBB2):c.91A>G (p.Met31Val)	not provided [RCV003728457]	uncertain significance	17	39707007	39707007	Human		name
405127295	CV3053684	single nucleotide variant	NM_004448.4(ERBB2):c.777C>T (p.Asn259=)	not provided [RCV003724495]	likely benign	17	39710357	39710357	Human		name
405243519	CV3053818	single nucleotide variant	NM_004448.4(ERBB2):c.312C>T (p.Gly104=)	not provided [RCV003719754]	likely benign	17	39708407	39708407	Human		name
405225263	CV3058230	microsatellite	NM_004448.4(ERBB2):c.1646+19_1646+20del	not provided [RCV003733855]	likely benign	17	39716449	39716450	Human		name
405224781	CV3058231	deletion	NM_004448.4(ERBB2):c.3160-15_3160-14del	not provided [RCV003733856]	likely benign	17	39727279	39727280	Human		name
405223468	CV3061303	microsatellite	NM_004448.4(ERBB2):c.1646+16_1646+18del	not provided [RCV003733669]	likely benign	17	39716445	39716447	Human		name
405160593	CV3062445	single nucleotide variant	NM_004448.4(ERBB2):c.873C>T (p.Phe291=)	not provided [RCV003727068]	likely benign	17	39710453	39710453	Human		name
405219214	CV3154229	single nucleotide variant	NM_004448.4(ERBB2):c.62C>G (p.Ala21Gly)	not provided [RCV003846921]	uncertain significance	17	39700300	39700300	Human		name
402477178	CV3173809	single nucleotide variant	NM_004448.4(ERBB2):c.396C>T (p.Ala132=)	not provided [RCV003875347]	likely benign	17	39708491	39708491	Human		name
597936469	CV3807650	single nucleotide variant	NM_004448.4(ERBB2):c.456G>C (p.Gly152=)	not provided [RCV005158029]	likely benign	17	39709334	39709334	Human		name
597945007	CV3844142	single nucleotide variant	NM_004448.4(ERBB2):c.735G>A (p.Thr245=)	not provided [RCV005188751]	likely benign	17	39710177	39710177	Human		name
597945794	CV3844950	single nucleotide variant	NM_004448.4(ERBB2):c.573C>T (p.Ala191=)	not provided [RCV005188936]	uncertain significance	17	39709451	39709451	Human		name
597942721	CV3847317	single nucleotide variant	NM_004448.4(ERBB2):c.990G>T (p.Arg330=)	not provided [RCV005188236]	likely benign	17	39712016	39712016	Human		name
597942904	CV3847362	single nucleotide variant	NM_004448.4(ERBB2):c.48G>T (p.Leu16Phe)	not provided [RCV005188281]	uncertain significance	17	39700286	39700286	Human		name
15193102	CV704113	single nucleotide variant	NM_004448.4(ERBB2):c.528C>T (p.Asn176=)	not provided [RCV000955273]	benign	17	39709406	39709406	Human		name
15149340	CV727134	single nucleotide variant	NM_004448.4(ERBB2):c.381C>G (p.Thr127=)	not provided [RCV000879145]	benign	17	39708476	39708476	Human		name
15200290	CV755809	single nucleotide variant	NM_004448.4(ERBB2):c.345C>T (p.Ala115=)	not provided [RCV000912803]	benign	17	39708440	39708440	Human		name
15106095	CV771469	single nucleotide variant	NM_004448.4(ERBB2):c.591G>A (p.Pro197=)	not provided [RCV000937719]	likely benign	17	39709829	39709829	Human		name
15188685	CV771470	single nucleotide variant	NM_004448.4(ERBB2):c.648G>A (p.Thr216=)	not provided [RCV000932020]	likely benign	17	39710090	39710090	Human		name
127276177	CV1082970	single nucleotide variant	NM_004448.4(ERBB2):c.1065A>G (p.Ala355=)	not provided [RCV001407075]	likely benign	17	39712365	39712365	Human		name
127241356	CV1082972	single nucleotide variant	NM_004448.4(ERBB2):c.1713T>C (p.Asn571=)	not provided [RCV001393129]	likely benign	17	39716581	39716581	Human		name
127242169	CV1082974	single nucleotide variant	NM_004448.4(ERBB2):c.2724T>C (p.Tyr908=)	not provided [RCV001415925]	likely benign	17	39725401	39725401	Human		name
127275830	CV1104768	single nucleotide variant	NM_004448.4(ERBB2):c.1269C>T (p.Ser423=)	not provided [RCV001443510]	likely benign	17	39715492	39715492	Human		name
127264556	CV1104769	single nucleotide variant	NM_004448.4(ERBB2):c.1317C>T (p.Gly439=)	not provided [RCV001428883]	likely benign	17	39715743	39715743	Human		name
127263936	CV1104770	single nucleotide variant	NM_004448.4(ERBB2):c.1659G>A (p.Glu553=)	not provided [RCV001428699]	likely benign	17	39716527	39716527	Human		name
127278793	CV1104772	single nucleotide variant	NM_004448.4(ERBB2):c.2769C>T (p.Tyr923=)	not provided [RCV001445323]	likely benign	17	39725750	39725750	Human		name
127245197	CV1104773	single nucleotide variant	NM_004448.4(ERBB2):c.2914T>C (p.Leu972=)	not provided [RCV001424260]	likely benign	17	39726603	39726603	Human		name
127306112	CV1126185	single nucleotide variant	NM_004448.4(ERBB2):c.1389T>C (p.Ser463=)	not provided [RCV001455403]	likely benign	17	39715815	39715815	Human		name
127289987	CV1126186	single nucleotide variant	NM_004448.4(ERBB2):c.1746C>T (p.Asp582=)	not provided [RCV001458295]	likely benign	17	39717328	39717328	Human		name
127305736	CV1126187	single nucleotide variant	NM_004448.4(ERBB2):c.2172G>A (p.Lys724=)	not provided [RCV001455318]	likely benign	17	39723624	39723624	Human		name
127302593	CV1126188	single nucleotide variant	NM_004448.4(ERBB2):c.2400T>C (p.Leu800=)	not provided [RCV001461678]	likely benign	17	39724818	39724818	Human		name
127315513	CV1147084	single nucleotide variant	NM_004448.4(ERBB2):c.1725C>T (p.Thr575=)	not provided [RCV001502740]	likely benign	17	39716593	39716593	Human		name
127331171	CV1147086	single nucleotide variant	NM_004448.4(ERBB2):c.2472C>T (p.Asn824=)	not provided [RCV001488638]	likely benign	17	39724890	39724890	Human		name
127333699	CV1147087	single nucleotide variant	NM_004448.4(ERBB2):c.2536T>C (p.Leu846=)	not provided [RCV001490336]	likely benign	17	39725091	39725091	Human		name
127304857	CV1147088	single nucleotide variant	NM_004448.4(ERBB2):c.2541C>T (p.Ala847=)	not provided [RCV001499764]	likely benign	17	39725096	39725096	Human		name
127332276	CV1147089	single nucleotide variant	NM_004448.4(ERBB2):c.2688C>T (p.Arg896=)	not provided [RCV001489396]	likely benign	17	39725365	39725365	Human		name
127309391	CV1157954	single nucleotide variant	NM_004448.4(ERBB2):c.1371A>G (p.Ser457=)	not provided [RCV001517870]	benign	17	39715797	39715797	Human		name
127292772	CV1157955	single nucleotide variant	NM_004448.4(ERBB2):c.1416C>T (p.Thr472=)	not provided [RCV001510977]	benign	17	39715842	39715842	Human		name
127304647	CV1157956	single nucleotide variant	NM_004448.4(ERBB2):c.1467G>A (p.Pro489=)	not provided [RCV001515984]	benign	17	39715893	39715893	Human		name
127297528	CV1157957	single nucleotide variant	NM_004448.4(ERBB2):c.1932C>T (p.Ala644=)	not provided [RCV001512913]	benign	17	39719820	39719820	Human		name
127300630	CV1157958	single nucleotide variant	NM_004448.4(ERBB2):c.2379G>A (p.Thr793=)	not provided [RCV001514259]	benign	17	39724797	39724797	Human		name
151760984	CV1349457	single nucleotide variant	NM_004448.4(ERBB2):c.206C>G (p.Ala69Gly)	not provided [RCV001949137]	uncertain significance	17	39707122	39707122	Human		name
151848201	CV1353004	single nucleotide variant	NM_004448.4(ERBB2):c.223C>T (p.Gln75Ter)	not provided [RCV001922413]	uncertain significance	17	39707139	39707139	Human		name
151863385	CV1353650	single nucleotide variant	NM_004448.4(ERBB2):c.170A>G (p.Gln57Arg)	not provided [RCV001924300]	uncertain significance	17	39707086	39707086	Human		name
151667740	CV1354081	single nucleotide variant	NM_004448.4(ERBB2):c.152A>G (p.Gln51Arg)	not provided [RCV001963823]\|not specified [RCV004907759]	uncertain significance	17	39707068	39707068	Human		name
151872978	CV1359419	single nucleotide variant	NM_004448.4(ERBB2):c.199A>G (p.Thr67Ala)	Glioma susceptibility 1 [RCV005017036]\|not provided [RCV002019187]	uncertain significance	17	39707115	39707115	Human	4	name
151848319	CV1362103	single nucleotide variant	NM_004448.4(ERBB2):c.1437G>A (p.Thr479=)	not provided [RCV001937018]	uncertain significance	17	39715863	39715863	Human		name
8688907	CV136694	single nucleotide variant	NM_004448.4(ERBB2):c.2506C>T (p.Leu836=)	Endometrial carcinoma [RCV000119346]	not provided	17	39725061	39725061	Human		name
8688908	CV136695	single nucleotide variant	NM_004448.4(ERBB2):c.2520G>A (p.Arg840=)	Familial cancer of breast [RCV000119347]	not provided	17	39725075	39725075	Human		name
8688909	CV136696	single nucleotide variant	NM_004448.4(ERBB2):c.2568C>T (p.Pro856=)	Familial cancer of breast [RCV000119348]	not provided	17	39725123	39725123	Human		name
8688910	CV136697	single nucleotide variant	NM_004448.4(ERBB2):c.2605C>T (p.Leu869=)	Ovarian neoplasm [RCV000119349]	not provided	17	39725160	39725160	Human		name
8689219	CV137018	single nucleotide variant	NM_004448.4(ERBB2):c.2535C>T (p.Asp845=)	Familial cancer of breast [RCV000119789]	not provided	17	39725090	39725090	Human		name
151856890	CV1372791	single nucleotide variant	NM_004448.4(ERBB2):c.122C>T (p.Thr41Ile)	not provided [RCV002033886]	uncertain significance	17	39707038	39707038	Human		name
8687363	CV137813	single nucleotide variant	NM_004448.4(ERBB2):c.133A>G (p.Met45Val)	not specified [RCV000120745]	not provided	17	39707049	39707049	Human		name
8687364	CV137814	single nucleotide variant	NM_004448.4(ERBB2):c.140G>A (p.Arg47His)	not provided [RCV001517014]\|not specified [RCV000120746]	benign\|not provided	17	39707056	39707056	Human		name
8687376	CV137826	single nucleotide variant	NM_004448.4(ERBB2):c.236A>C (p.Glu79Ala)	not provided [RCV000901748]\|not specified [RCV000120758]	likely benign\|not provided	17	39708331	39708331	Human		name
151800486	CV1382046	single nucleotide variant	NM_004448.4(ERBB2):c.1797C>G (p.Arg599=)	not provided [RCV001952877]	likely benign\|uncertain significance	17	39717379	39717379	Human		name
151773497	CV1402845	single nucleotide variant	NM_004448.4(ERBB2):c.118G>A (p.Glu40Lys)	not provided [RCV001896569]	uncertain significance	17	39707034	39707034	Human		name
151861493	CV1423357	single nucleotide variant	NM_004448.4(ERBB2):c.203A>G (p.Asn68Ser)	not provided [RCV001997186]	uncertain significance	17	39707119	39707119	Human		name
151847502	CV1428299	single nucleotide variant	NM_004448.4(ERBB2):c.2307C>T (p.Asp769=)	not provided [RCV001957532]	uncertain significance	17	39724010	39724010	Human		name
151864088	CV1431499	single nucleotide variant	NM_004448.4(ERBB2):c.250G>A (p.Val84Met)	not provided [RCV001924385]	uncertain significance	17	39708345	39708345	Human		name
151848271	CV1441807	single nucleotide variant	NM_004448.4(ERBB2):c.202A>G (p.Asn68Asp)	not provided [RCV001995624]	uncertain significance	17	39707118	39707118	Human		name
152155491	CV1520313	single nucleotide variant	NM_004448.4(ERBB2):c.1509G>A (p.Glu503=)	not provided [RCV002140112]	likely benign	17	39715935	39715935	Human		name
152037044	CV1524816	single nucleotide variant	NM_004448.4(ERBB2):c.1545C>T (p.Cys515=)	not provided [RCV002165122]	likely benign	17	39716332	39716332	Human		name
152065154	CV1525926	single nucleotide variant	NM_004448.4(ERBB2):c.1113T>C (p.Phe371=)	not provided [RCV002128870]	benign	17	39712413	39712413	Human		name
152126763	CV1528092	single nucleotide variant	NM_004448.4(ERBB2):c.1686G>A (p.Pro562=)	not provided [RCV002098925]	likely benign	17	39716554	39716554	Human		name
152159102	CV1529191	single nucleotide variant	NM_004448.4(ERBB2):c.2130G>A (p.Ala710=)	not provided [RCV002159317]	likely benign	17	39723582	39723582	Human		name
152152868	CV1529778	single nucleotide variant	NM_004448.4(ERBB2):c.2346C>T (p.Val782=)	not provided [RCV002202249]	likely benign	17	39724764	39724764	Human		name
152157567	CV1541800	single nucleotide variant	NM_004448.4(ERBB2):c.2619C>T (p.Asp873=)	not provided [RCV002103167]	likely benign	17	39725174	39725174	Human		name
152175996	CV1562137	single nucleotide variant	NM_004448.4(ERBB2):c.1755G>A (p.Val585=)	not provided [RCV002164136]	likely benign	17	39717337	39717337	Human		name
152173796	CV1567223	single nucleotide variant	NM_004448.4(ERBB2):c.1929C>T (p.Pro643=)	not provided [RCV002144230]	likely benign	17	39719817	39719817	Human		name
152113947	CV1573579	single nucleotide variant	NM_004448.4(ERBB2):c.2628G>A (p.Glu876=)	not provided [RCV002215875]	likely benign	17	39725183	39725183	Human		name
152114584	CV1574915	single nucleotide variant	NM_004448.4(ERBB2):c.2442C>T (p.Arg814=)	not provided [RCV002117010]	likely benign	17	39724860	39724860	Human		name
152064929	CV1576065	single nucleotide variant	NM_004448.4(ERBB2):c.2574T>C (p.His858=)	not provided [RCV002209192]	likely benign	17	39725129	39725129	Human		name
152153102	CV1592006	single nucleotide variant	NM_004448.4(ERBB2):c.1782C>A (p.Pro594=)	not provided [RCV002102537]	likely benign	17	39717364	39717364	Human		name
152119191	CV1593607	single nucleotide variant	NM_004448.4(ERBB2):c.2743C>T (p.Leu915=)	not provided [RCV002097916]	likely benign	17	39725724	39725724	Human		name
152102924	CV1606003	single nucleotide variant	NM_004448.4(ERBB2):c.1179G>A (p.Gln393=)	Glioma susceptibility 1 [RCV005017127]\|not provided [RCV002095765]	likely benign\|uncertain significance	17	39715316	39715316	Human	4	name
152028012	CV1607638	single nucleotide variant	NM_004448.4(ERBB2):c.2727T>G (p.Gly909=)	not provided [RCV002105089]	likely benign	17	39725708	39725708	Human		name
152087610	CV1608559	single nucleotide variant	NM_004448.4(ERBB2):c.1383G>A (p.Leu461=)	not provided [RCV002212265]	likely benign	17	39715809	39715809	Human		name
152127189	CV1615176	single nucleotide variant	NM_004448.4(ERBB2):c.2796T>C (p.Pro932=)	not provided [RCV002082377]	likely benign	17	39725777	39725777	Human		name
152075204	CV1616642	single nucleotide variant	NM_004448.4(ERBB2):c.1051C>A (p.Arg351=)	not provided [RCV002210500]	likely benign	17	39712351	39712351	Human		name
152032249	CV1624770	single nucleotide variant	NM_004448.4(ERBB2):c.1620C>T (p.Cys540=)	not provided [RCV002186858]	likely benign	17	39716407	39716407	Human		name
152096394	CV1627902	single nucleotide variant	NM_004448.4(ERBB2):c.1662T>C (p.Tyr554=)	not provided [RCV002194977]	likely benign	17	39716530	39716530	Human		name
152115415	CV1637181	single nucleotide variant	NM_004448.4(ERBB2):c.1476T>C (p.Ala492=)	not provided [RCV002216064]	likely benign	17	39715902	39715902	Human		name
152167637	CV1644773	single nucleotide variant	NM_004448.4(ERBB2):c.1083C>A (p.Ile361=)	not provided [RCV002142209]	likely benign	17	39712383	39712383	Human		name
152117112	CV1645887	single nucleotide variant	NM_004448.4(ERBB2):c.2973T>C (p.Asn991=)	not provided [RCV002175080]	likely benign	17	39726817	39726817	Human		name
152117201	CV1645902	single nucleotide variant	NM_004448.4(ERBB2):c.1428C>T (p.Phe476=)	not provided [RCV002175091]	likely benign	17	39715854	39715854	Human		name
152043529	CV1650895	single nucleotide variant	NM_004448.4(ERBB2):c.1875T>C (p.Pro625=)	not provided [RCV002166002]	likely benign	17	39717457	39717457	Human		name
152068188	CV1653981	single nucleotide variant	NM_004448.4(ERBB2):c.1681T>C (p.Leu561=)	not provided [RCV002111086]	likely benign	17	39716549	39716549	Human		name
152166383	CV1661269	single nucleotide variant	NM_004448.4(ERBB2):c.1908C>T (p.Asp636=)	not provided [RCV002124215]	likely benign	17	39719796	39719796	Human		name
156058972	CV1876092	single nucleotide variant	NM_004448.4(ERBB2):c.100C>T (p.Arg34Trp)	not provided [RCV003053273]	uncertain significance	17	39707016	39707016	Human		name
155943374	CV1878790	single nucleotide variant	NM_004448.4(ERBB2):c.2607G>A (p.Leu869=)	not provided [RCV003073691]	likely benign	17	39725162	39725162	Human		name
156078657	CV1886664	single nucleotide variant	NM_004448.4(ERBB2):c.2158C>T (p.Leu720=)	not provided [RCV003079790]	likely benign	17	39723610	39723610	Human		name
156098115	CV1896610	single nucleotide variant	NM_004448.4(ERBB2):c.1506C>T (p.Asp502=)	not provided [RCV003080493]	likely benign	17	39715932	39715932	Human		name
156198810	CV1897353	single nucleotide variant	NM_004448.4(ERBB2):c.1650C>T (p.Leu550=)	not provided [RCV002574670]	likely benign	17	39716518	39716518	Human		name
156404611	CV1898327	single nucleotide variant	NM_004448.4(ERBB2):c.1347C>T (p.Gly449=)	not provided [RCV002585447]	likely benign	17	39715773	39715773	Human		name
156362232	CV1899107	single nucleotide variant	NM_004448.4(ERBB2):c.2523C>T (p.Leu841=)	not provided [RCV003091789]	likely benign	17	39725078	39725078	Human		name
156361934	CV1900615	single nucleotide variant	NM_004448.4(ERBB2):c.1134G>A (p.Pro378=)	not provided [RCV002581785]	likely benign	17	39712434	39712434	Human		name
156362201	CV1900645	single nucleotide variant	NM_004448.4(ERBB2):c.2451G>T (p.Leu817=)	not provided [RCV002581802]	likely benign	17	39724869	39724869	Human		name
156362246	CV1900648	single nucleotide variant	NM_004448.4(ERBB2):c.2280C>T (p.Ser760=)	not provided [RCV002581805]	likely benign	17	39723983	39723983	Human		name
156378957	CV1903212	single nucleotide variant	NM_004448.4(ERBB2):c.1698G>A (p.Glu566=)	not provided [RCV003093115]	likely benign	17	39716566	39716566	Human		name
156316625	CV1903690	single nucleotide variant	NM_004448.4(ERBB2):c.1677C>T (p.His559=)	not provided [RCV003088758]	likely benign	17	39716545	39716545	Human		name
156317312	CV1903818	single nucleotide variant	NM_004448.4(ERBB2):c.2715G>A (p.Val905=)	not provided [RCV003088796]	uncertain significance	17	39725392	39725392	Human		name
156358688	CV1904127	single nucleotide variant	NM_004448.4(ERBB2):c.131A>T (p.Asp44Val)	not provided [RCV002581573]	uncertain significance	17	39707047	39707047	Human		name
156359011	CV1904171	single nucleotide variant	NM_004448.4(ERBB2):c.1335G>A (p.Leu445=)	not provided [RCV002581596]	likely benign	17	39715761	39715761	Human		name
156412721	CV1904564	single nucleotide variant	NM_004448.4(ERBB2):c.1119C>T (p.Ser373=)	not provided [RCV002587922]	likely benign	17	39712419	39712419	Human		name
156378283	CV1906861	single nucleotide variant	NM_004448.4(ERBB2):c.2004G>C (p.Gly668=)	not provided [RCV003093057]	likely benign	17	39723376	39723376	Human		name
156366000	CV1909269	single nucleotide variant	NM_004448.4(ERBB2):c.2592C>T (p.Phe864=)	not provided [RCV002602831]	likely benign	17	39725147	39725147	Human		name
156417227	CV1915842	single nucleotide variant	NM_004448.4(ERBB2):c.1815A>G (p.Lys605=)	not provided [RCV002610608]	likely benign	17	39717397	39717397	Human		name
156199527	CV1916673	single nucleotide variant	NM_004448.4(ERBB2):c.233A>G (p.Gln78Arg)	not provided [RCV002595652]	uncertain significance	17	39708328	39708328	Human		name
156017492	CV1918492	single nucleotide variant	NM_004448.4(ERBB2):c.2931C>T (p.Ser977=)	not provided [RCV002636542]	likely benign	17	39726620	39726620	Human		name
156369062	CV1919956	single nucleotide variant	NM_004448.4(ERBB2):c.2316C>T (p.Tyr772=)	not provided [RCV002603034]	likely benign	17	39724734	39724734	Human		name
156405893	CV1921389	single nucleotide variant	NM_004448.4(ERBB2):c.1242A>C (p.Ala414=)	not provided [RCV002606437]	likely benign	17	39715465	39715465	Human		name
156444108	CV1937631	single nucleotide variant	NM_004448.4(ERBB2):c.1581G>A (p.Gln527=)	not provided [RCV003115027]	likely benign	17	39716368	39716368	Human		name
156444677	CV1948405	single nucleotide variant	NM_004448.4(ERBB2):c.2010C>G (p.Val670=)	not provided [RCV003115602]	likely benign	17	39723382	39723382	Human		name
156385882	CV1971991	single nucleotide variant	NM_004448.4(ERBB2):c.1207C>T (p.Leu403=)	not provided [RCV002604291]	likely benign	17	39715344	39715344	Human		name
156321520	CV2022099	single nucleotide variant	NM_004448.4(ERBB2):c.1176C>G (p.Leu392=)	not provided [RCV002717122]	likely benign	17	39715313	39715313	Human		name
155991094	CV2026975	single nucleotide variant	NM_004448.4(ERBB2):c.1872G>A (p.Gln624=)	not provided [RCV002755752]	likely benign	17	39717454	39717454	Human		name
156024658	CV2043396	single nucleotide variant	NM_004448.4(ERBB2):c.1629A>G (p.Glu543=)	not provided [RCV002780831]	likely benign	17	39716416	39716416	Human		name
156143882	CV2044622	single nucleotide variant	NM_004448.4(ERBB2):c.2589C>T (p.Asp863=)	not provided [RCV002801056]	uncertain significance	17	39725144	39725144	Human		name
156327031	CV2054211	single nucleotide variant	NM_004448.4(ERBB2):c.1999T>C (p.Leu667=)	not provided [RCV002810454]	likely benign	17	39723371	39723371	Human		name
401914230	CV2811299	single nucleotide variant	NM_004448.4(ERBB2):c.2967C>T (p.Ile989=)	not provided [RCV003428254]	likely benign	17	39726656	39726656	Human		name
405171098	CV2854438	single nucleotide variant	NM_004448.4(ERBB2):c.2109C>T (p.Ser703=)	not provided [RCV003542171]	likely benign	17	39723561	39723561	Human		name
405128771	CV2893185	single nucleotide variant	NM_004448.4(ERBB2):c.1152C>T (p.Asp384=)	not provided [RCV003559757]	likely benign	17	39715289	39715289	Human		name
405249342	CV3000563	single nucleotide variant	NM_004448.4(ERBB2):c.271G>C (p.Val91Leu)	not provided [RCV003721284]	uncertain significance	17	39708366	39708366	Human		name
405092415	CV3044661	single nucleotide variant	NM_004448.4(ERBB2):c.2379G>C (p.Thr793=)	not provided [RCV003717706]	likely benign	17	39724797	39724797	Human		name
405253795	CV3044997	single nucleotide variant	NM_004448.4(ERBB2):c.193C>A (p.Leu65Met)	not provided [RCV003722697]	uncertain significance	17	39707109	39707109	Human		name
405217347	CV3048823	single nucleotide variant	NM_004448.4(ERBB2):c.2292C>T (p.Asn764=)	not provided [RCV003732824]	likely benign	17	39723995	39723995	Human		name
405217380	CV3048834	single nucleotide variant	NM_004448.4(ERBB2):c.1317C>G (p.Gly439=)	not provided [RCV003732828]	likely benign	17	39715743	39715743	Human		name
405243861	CV3053951	single nucleotide variant	NM_004448.4(ERBB2):c.1788C>T (p.Cys596=)	not provided [RCV003719836]	likely benign	17	39717370	39717370	Human		name
405207489	CV3064632	single nucleotide variant	NM_004448.4(ERBB2):c.2997C>T (p.Pro999=)	not provided [RCV003731523]	likely benign	17	39726841	39726841	Human		name
405205426	CV3068182	single nucleotide variant	NM_004448.4(ERBB2):c.268C>A (p.Gln90Lys)	not provided [RCV003731271]	uncertain significance	17	39708363	39708363	Human		name
405131542	CV3115110	single nucleotide variant	NM_004448.4(ERBB2):c.1068T>C (p.Val356=)	not provided [RCV003815955]	likely benign	17	39712368	39712368	Human		name
405112172	CV3118502	single nucleotide variant	NM_004448.4(ERBB2):c.1458T>C (p.Phe486=)	not provided [RCV003813730]	likely benign	17	39715884	39715884	Human		name
405074843	CV3156107	single nucleotide variant	NM_004448.4(ERBB2):c.112A>G (p.Ser38Gly)	not provided [RCV003851165]	uncertain significance	17	39707028	39707028	Human		name
405226897	CV3169500	single nucleotide variant	NM_004448.4(ERBB2):c.2283C>G (p.Pro761=)	not provided [RCV003864524]	likely benign	17	39723986	39723986	Human		name
402482734	CV3170901	single nucleotide variant	NM_004448.4(ERBB2):c.2991C>T (p.Ala997=)	not provided [RCV003876104]	likely benign	17	39726835	39726835	Human		name
597878780	CV3744416	single nucleotide variant	NM_004448.4(ERBB2):c.2154G>T (p.Thr718=)	not provided [RCV005069630]	likely benign	17	39723606	39723606	Human		name
597861790	CV3766399	single nucleotide variant	NM_004448.4(ERBB2):c.2610G>A (p.Leu870=)	not provided [RCV005106124]	likely benign	17	39725165	39725165	Human		name
597973719	CV3801545	single nucleotide variant	NM_004448.4(ERBB2):c.1215G>A (p.Glu405=)	not provided [RCV005143534]	likely benign	17	39715352	39715352	Human		name
597922348	CV3808161	single nucleotide variant	NM_004448.4(ERBB2):c.1062G>A (p.Arg354=)	not provided [RCV005155869]	likely benign	17	39712362	39712362	Human		name
597955964	CV3838102	single nucleotide variant	NM_004448.4(ERBB2):c.2145G>T (p.Leu715=)	not provided [RCV005191476]	likely benign	17	39723597	39723597	Human		name
597962594	CV3841031	single nucleotide variant	NM_004448.4(ERBB2):c.1806C>T (p.Ser602=)	not provided [RCV005193324]	likely benign	17	39717388	39717388	Human		name
597960418	CV3843651	single nucleotide variant	NM_004448.4(ERBB2):c.2670G>A (p.Ala890=)	not provided [RCV005192688]	likely benign	17	39725347	39725347	Human		name
597933247	CV3844626	single nucleotide variant	NM_004448.4(ERBB2):c.1107G>A (p.Lys369=)	not provided [RCV005186132]	likely benign	17	39712407	39712407	Human		name
597943534	CV3847207	single nucleotide variant	NM_004448.4(ERBB2):c.2550C>T (p.Asn850=)	not provided [RCV005188127]	likely benign	17	39725105	39725105	Human		name
597958539	CV3848449	single nucleotide variant	NM_004448.4(ERBB2):c.259G>A (p.Ala87Thr)	not provided [RCV005192150]	uncertain significance	17	39708354	39708354	Human		name
597904802	CV3853025	single nucleotide variant	NM_004448.4(ERBB2):c.1686G>T (p.Pro562=)	not provided [RCV005202682]	likely benign	17	39716554	39716554	Human		name
598170014	CV3961648	single nucleotide variant	NM_004448.4(ERBB2):c.264C>A (p.His88Gln)	not specified [RCV005330604]	uncertain significance	17	39708359	39708359	Human		name
15149347	CV727135	single nucleotide variant	NM_004448.4(ERBB2):c.1326G>T (p.Ser442=)	not provided [RCV000879146]	benign	17	39715752	39715752	Human		name
15128791	CV740711	single nucleotide variant	NM_004448.4(ERBB2):c.1569A>G (p.Pro523=)	not provided [RCV000897335]	benign	17	39716356	39716356	Human		name
15134322	CV740712	single nucleotide variant	NM_004448.4(ERBB2):c.1863C>T (p.Gly621=)	not provided [RCV000898268]	likely benign	17	39717445	39717445	Human		name
15171326	CV740713	single nucleotide variant	NM_004448.4(ERBB2):c.2148A>G (p.Lys716=)	not provided [RCV000905445]	benign	17	39723600	39723600	Human		name
15101477	CV755810	single nucleotide variant	NM_004448.4(ERBB2):c.1248G>A (p.Pro416=)	not provided [RCV000914788]	likely benign	17	39715471	39715471	Human		name
15197265	CV755811	single nucleotide variant	NM_004448.4(ERBB2):c.1317C>A (p.Gly439=)	not provided [RCV000911928]	likely benign	17	39715743	39715743	Human		name
15168794	CV755812	single nucleotide variant	NM_004448.4(ERBB2):c.2826C>T (p.Pro942=)	not provided [RCV000927368]	likely benign	17	39725807	39725807	Human		name
26894141	CV845259	single nucleotide variant	NM_004448.4(ERBB2):c.1518C>T (p.Gly506=)	not provided [RCV001063238]	likely benign\|uncertain significance	17	39716305	39716305	Human		name
126771766	CV1012730	single nucleotide variant	NM_004448.4(ERBB2):c.298C>T (p.Arg100Trp)	not provided [RCV001323347]	uncertain significance	17	39708393	39708393	Human		name
126773701	CV1033255	single nucleotide variant	NM_004448.4(ERBB2):c.874G>A (p.Gly292Ser)	not provided [RCV001346378]	uncertain significance	17	39710454	39710454	Human		name
126922042	CV1050221	single nucleotide variant	NM_004448.4(ERBB2):c.343G>A (p.Ala115Thr)	not provided [RCV001364199]	uncertain significance	17	39708438	39708438	Human		name
127242179	CV1082975	single nucleotide variant	NM_004448.4(ERBB2):c.3036T>C (p.Asp1012=)	not provided [RCV001415926]	likely benign	17	39726880	39726880	Human		name
127240362	CV1082976	single nucleotide variant	NM_004448.4(ERBB2):c.3081G>A (p.Gln1027=)	not provided [RCV001415543]	likely benign	17	39726925	39726925	Human		name
127252582	CV1082977	single nucleotide variant	NM_004448.4(ERBB2):c.3268C>T (p.Leu1090=)	not provided [RCV001418110]	likely benign	17	39727403	39727403	Human		name
127249933	CV1082978	single nucleotide variant	NM_004448.4(ERBB2):c.3453G>A (p.Ser1151=)	not provided [RCV001399739]	likely benign	17	39727729	39727729	Human		name
127254470	CV1082979	single nucleotide variant	NM_004448.4(ERBB2):c.3540C>T (p.Val1180=)	not provided [RCV001418566]	likely benign	17	39727816	39727816	Human		name
127252028	CV1082980	single nucleotide variant	NM_004448.4(ERBB2):c.3651C>T (p.Phe1217=)	not provided [RCV001417957]	likely benign	17	39727927	39727927	Human		name
127236637	CV1104775	single nucleotide variant	NM_004448.4(ERBB2):c.3591G>A (p.Leu1197=)	not provided [RCV001433383]	likely benign	17	39727867	39727867	Human		name
127298415	CV1126184	single nucleotide variant	NM_004448.4(ERBB2):c.808G>T (p.Ala270Ser)	not provided [RCV001460554]	likely benign	17	39710388	39710388	Human		name
127324375	CV1126190	single nucleotide variant	NM_004448.4(ERBB2):c.3156C>G (p.Thr1052=)	not provided [RCV001468191]	likely benign	17	39727000	39727000	Human		name
127295763	CV1126191	single nucleotide variant	NM_004448.4(ERBB2):c.3396C>T (p.Thr1132=)	not provided [RCV001459812]	likely benign	17	39727531	39727531	Human		name
127318459	CV1126192	single nucleotide variant	NM_004448.4(ERBB2):c.3441C>T (p.Pro1147=)	not provided [RCV001466213]	likely benign	17	39727717	39727717	Human		name
127305827	CV1126193	single nucleotide variant	NM_004448.4(ERBB2):c.3741G>A (p.Glu1247=)	not provided [RCV001462597]	likely benign	17	39728017	39728017	Human		name
127313048	CV1157959	single nucleotide variant	NM_004448.4(ERBB2):c.3070C>T (p.Leu1024=)	not provided [RCV001519140]	benign	17	39726914	39726914	Human		name
127316469	CV1157960	single nucleotide variant	NM_004448.4(ERBB2):c.3108C>T (p.Ala1036=)	not provided [RCV001520501]	benign	17	39726952	39726952	Human		name
150543199	CV1309358	single nucleotide variant	NM_004448.4(ERBB2):c.563G>A (p.Arg188His)	not provided [RCV001885104]	uncertain significance	17	39709441	39709441	Human		name
151862227	CV1338644	single nucleotide variant	NM_004448.4(ERBB2):c.569G>C (p.Arg190Pro)	not provided [RCV001997278]	uncertain significance	17	39709447	39709447	Human		name
151793967	CV1341042	single nucleotide variant	NM_004448.4(ERBB2):c.568C>T (p.Arg190Trp)	not provided [RCV001931683]	uncertain significance	17	39709446	39709446	Human		name
151803700	CV1352647	single nucleotide variant	NM_004448.4(ERBB2):c.455G>C (p.Gly152Ala)	Glioma susceptibility 1 [RCV005014740]\|not provided [RCV001899302]	uncertain significance	17	39709333	39709333	Human	4	name
151759785	CV1355380	single nucleotide variant	NM_004448.4(ERBB2):c.608G>A (p.Arg203His)	Glioma susceptibility 1 [RCV005016899]\|not provided [RCV001949002]	uncertain significance	17	39709846	39709846	Human	4	name
151851545	CV1362193	single nucleotide variant	NM_004448.4(ERBB2):c.370A>T (p.Asn124Tyr)	not provided [RCV001979008]	uncertain significance	17	39708465	39708465	Human		name
151771502	CV1366396	single nucleotide variant	NM_004448.4(ERBB2):c.776A>G (p.Asn259Ser)	not provided [RCV001929561]	uncertain significance	17	39710356	39710356	Human		name
151771615	CV1366409	single nucleotide variant	NM_004448.4(ERBB2):c.769C>T (p.His257Tyr)	not provided [RCV001929571]	uncertain significance	17	39710349	39710349	Human		name
151789203	CV1377160	single nucleotide variant	NM_004448.4(ERBB2):c.607C>T (p.Arg203Cys)	not provided [RCV001898013]	uncertain significance	17	39709845	39709845	Human		name
8687377	CV137827	single nucleotide variant	NM_004448.4(ERBB2):c.383C>G (p.Pro128Arg)	not provided [RCV002517586]\|not specified [RCV000120759]	uncertain significance\|not provided	17	39708478	39708478	Human		name
8687378	CV137828	single nucleotide variant	NM_004448.4(ERBB2):c.433C>T (p.Leu145Phe)	not provided [RCV001461359]\|not specified [RCV000120760]	likely benign\|not provided	17	39708528	39708528	Human		name
8687379	CV137829	single nucleotide variant	NM_004448.4(ERBB2):c.428G>A (p.Arg143Gln)	not provided [RCV001200119]\|not specified [RCV000120761]	benign\|likely benign\|not provided	17	39708523	39708523	Human		name
8687380	CV137830	single nucleotide variant	NM_004448.4(ERBB2):c.734C>T (p.Thr245Met)	Glioma susceptibility 1 [RCV005016415]\|not provided [RCV002517587]\|not specified [RCV000120762]	uncertain significance\|not provided	17	39710176	39710176	Human	4	name
8688688	CV139258	single nucleotide variant	NM_001289936.2(ERBB2):c.22C>A (p.Pro8Thr)	not specified [RCV000122379]	not provided	17	39699581	39699581	Human		name
151713551	CV1405226	single nucleotide variant	NM_004448.4(ERBB2):c.608G>C (p.Arg203Pro)	not provided [RCV001889872]	uncertain significance	17	39709846	39709846	Human		name
151768126	CV1410436	single nucleotide variant	NM_004448.4(ERBB2):c.649C>T (p.Arg217Cys)	Glioma susceptibility 1 [RCV005016925]\|not provided [RCV001987981]	uncertain significance	17	39710091	39710091	Human	4	name
151720408	CV1420833	single nucleotide variant	NM_004448.4(ERBB2):c.863G>A (p.Arg288Gln)	not provided [RCV002039992]	uncertain significance	17	39710443	39710443	Human		name
151861428	CV1423291	single nucleotide variant	NM_004448.4(ERBB2):c.3111G>A (p.Pro1037=)	not provided [RCV001980165]	likely benign\|uncertain significance	17	39726955	39726955	Human		name
151833949	CV1446725	single nucleotide variant	NM_004448.4(ERBB2):c.508A>C (p.Lys170Gln)	not provided [RCV002031083]	uncertain significance	17	39709386	39709386	Human		name
151769837	CV1454386	single nucleotide variant	NM_004448.4(ERBB2):c.664G>A (p.Gly222Ser)	not provided [RCV001950050]	uncertain significance	17	39710106	39710106	Human		name
151780078	CV1467845	single nucleotide variant	NM_004448.4(ERBB2):c.3501G>A (p.Leu1167=)	not provided [RCV001971998]	likely benign\|uncertain significance	17	39727777	39727777	Human		name
151809341	CV1483657	single nucleotide variant	NM_004448.4(ERBB2):c.400C>T (p.Pro134Ser)	not provided [RCV001918447]	uncertain significance	17	39708495	39708495	Human		name
151718691	CV1506801	single nucleotide variant	NM_004448.4(ERBB2):c.497C>T (p.Thr166Met)	not provided [RCV001909384]	uncertain significance	17	39709375	39709375	Human		name
152136062	CV1528413	single nucleotide variant	NM_004448.4(ERBB2):c.3582C>T (p.Pro1194=)	not provided [RCV002100133]	likely benign	17	39727858	39727858	Human		name
152137482	CV1563401	single nucleotide variant	NM_004448.4(ERBB2):c.3756C>T (p.Asp1252=)	not provided [RCV002200139]	likely benign	17	39728032	39728032	Human		name
152057558	CV1567324	single nucleotide variant	NM_004448.4(ERBB2):c.3423C>T (p.Asn1141=)	not provided [RCV002146412]	likely benign	17	39727699	39727699	Human		name
152051321	CV1569241	single nucleotide variant	NM_004448.4(ERBB2):c.3381C>T (p.Tyr1127=)	not provided [RCV002207556]	likely benign	17	39727516	39727516	Human		name
152047900	CV1569601	single nucleotide variant	NM_004448.4(ERBB2):c.3249C>A (p.Ser1083=)	not provided [RCV002126866]	likely benign	17	39727384	39727384	Human		name
152104788	CV1574857	single nucleotide variant	NM_004448.4(ERBB2):c.3570C>T (p.Ala1190=)	not provided [RCV002096009]	likely benign	17	39727846	39727846	Human		name
152054557	CV1610011	single nucleotide variant	NM_004448.4(ERBB2):c.3168T>C (p.Gly1056=)	not provided [RCV002167271]	likely benign	17	39727303	39727303	Human		name
152082155	CV1641480	single nucleotide variant	NM_004448.4(ERBB2):c.3033C>T (p.Asp1011=)	not provided [RCV002211560]	likely benign	17	39726877	39726877	Human		name
152152988	CV1664610	single nucleotide variant	NM_004448.4(ERBB2):c.3201A>G (p.Glu1067=)	not provided [RCV002158467]	likely benign	17	39727336	39727336	Human		name
156223818	CV1879474	single nucleotide variant	NM_004448.4(ERBB2):c.3459A>C (p.Arg1153=)	not provided [RCV003059047]	likely benign	17	39727735	39727735	Human		name
156359142	CV1897954	single nucleotide variant	NM_004448.4(ERBB2):c.332A>G (p.Asn111Ser)	not provided [RCV002602372]	uncertain significance	17	39708427	39708427	Human		name
156380157	CV1899632	single nucleotide variant	NM_004448.4(ERBB2):c.3726G>A (p.Thr1242=)	not provided [RCV003093208]	likely benign	17	39728002	39728002	Human		name
156031144	CV1899634	single nucleotide variant	NM_004448.4(ERBB2):c.569G>A (p.Arg190Gln)	Glioma susceptibility 1 [RCV005021566]\|not provided [RCV003100655]	uncertain significance	17	39709447	39709447	Human	4	name
156221146	CV1899796	single nucleotide variant	NM_004448.4(ERBB2):c.562C>T (p.Arg188Cys)	Glioma susceptibility 1 [RCV005021568]\|not provided [RCV003085002]	uncertain significance	17	39709440	39709440	Human	4	name
156273207	CV1900054	single nucleotide variant	NM_004448.4(ERBB2):c.3573G>A (p.Val1191=)	Glioma susceptibility 1 [RCV005021573]\|not provided [RCV003086860]	likely benign\|uncertain significance	17	39727849	39727849	Human	4	name
156195362	CV1900656	single nucleotide variant	NM_004448.4(ERBB2):c.650G>A (p.Arg217His)	not provided [RCV002574550]	uncertain significance	17	39710092	39710092	Human		name
156368080	CV1904880	single nucleotide variant	NM_004448.4(ERBB2):c.590C>T (p.Pro197Leu)	not provided [RCV002582215]	uncertain significance	17	39709828	39709828	Human		name
156361517	CV1904897	single nucleotide variant	NM_004448.4(ERBB2):c.3006C>T (p.Ser1002=)	not provided [RCV002602531]	likely benign	17	39726850	39726850	Human		name
156101858	CV1907156	single nucleotide variant	NM_004448.4(ERBB2):c.677G>A (p.Arg226His)	not provided [RCV003080631]	uncertain significance	17	39710119	39710119	Human		name
155930674	CV1909013	single nucleotide variant	NM_004448.4(ERBB2):c.602G>T (p.Gly201Val)	not provided [RCV002614977]	uncertain significance	17	39709840	39709840	Human		name
156434934	CV1940265	single nucleotide variant	NM_004448.4(ERBB2):c.3114C>T (p.Gly1038=)	not provided [RCV003104677]	likely benign	17	39726958	39726958	Human		name
156168215	CV1993488	single nucleotide variant	NM_004448.4(ERBB2):c.580C>T (p.Pro194Ser)	not provided [RCV002642642]	uncertain significance	17	39709818	39709818	Human		name
156245803	CV1996560	single nucleotide variant	NM_004448.4(ERBB2):c.766C>T (p.Leu256Phe)	not provided [RCV002668087]	uncertain significance	17	39710346	39710346	Human		name
156272644	CV2004226	single nucleotide variant	NM_004448.4(ERBB2):c.594G>A (p.Met198Ile)	not provided [RCV002646583]	uncertain significance	17	39709832	39709832	Human		name
156083180	CV2023677	indel	NM_004448.4(ERBB2):c.3405_3412+42delinsAG	not provided [RCV002760692]	uncertain significance	17	39727540	39727589	Human		name
155942063	CV2034622	single nucleotide variant	NM_004448.4(ERBB2):c.877G>A (p.Ala293Thr)	not provided [RCV002775259]	uncertain significance	17	39710457	39710457	Human		name
156108340	CV2145820	single nucleotide variant	NM_004448.4(ERBB2):c.3174C>T (p.Asp1058=)	not provided [RCV003021306]	likely benign	17	39727309	39727309	Human		name
156080419	CV2173782	single nucleotide variant	NM_004448.4(ERBB2):c.821A>G (p.Tyr274Cys)	not provided [RCV003054009]	uncertain significance	17	39710401	39710401	Human		name
156001958	CV2179136	single nucleotide variant	NM_004448.4(ERBB2):c.3534T>C (p.Asn1178=)	not provided [RCV003034820]	likely benign	17	39727810	39727810	Human		name
156388267	CV2231753	single nucleotide variant	NM_004448.4(ERBB2):c.521A>G (p.His174Arg)	not specified [RCV004098569]	uncertain significance	17	39709399	39709399	Human		name
156196490	CV2337970	single nucleotide variant	NM_004448.4(ERBB2):c.605C>T (p.Ser202Phe)	not specified [RCV004186015]	uncertain significance	17	39709843	39709843	Human		name
401873863	CV2749861	single nucleotide variant	NM_004448.4(ERBB2):c.925G>A (p.Gly309Arg)	Malignant tumor of urinary bladder [RCV003332989]	pathogenic	17	39711951	39711951	Human	2	name
405213241	CV2878824	single nucleotide variant	NM_004448.4(ERBB2):c.462G>C (p.Leu154Phe)	not provided [RCV003552863]	uncertain significance	17	39709340	39709340	Human		name
405069967	CV2944709	duplication	NM_004448.4(ERBB2):c.2950dup (p.Gln984fs)	not provided [RCV003663859]	uncertain significance	17	39726634	39726635	Human		name
402493601	CV2982067	single nucleotide variant	NM_004448.4(ERBB2):c.929C>G (p.Ser310Cys)	not provided [RCV003714019]	uncertain significance	17	39711955	39711955	Human		name
405196089	CV3037659	single nucleotide variant	NM_004448.4(ERBB2):c.528C>A (p.Asn176Lys)	not provided [RCV003706927]	uncertain significance	17	39709406	39709406	Human		name
405225517	CV3042195	single nucleotide variant	NM_004448.4(ERBB2):c.3648C>G (p.Ala1216=)	not provided [RCV003710629]	likely benign	17	39727924	39727924	Human		name
405253157	CV3044314	single nucleotide variant	NM_004448.4(ERBB2):c.3234C>T (p.Ser1078=)	not provided [RCV003722442]	likely benign	17	39727369	39727369	Human		name
405081859	CV3046637	single nucleotide variant	NM_004448.4(ERBB2):c.3249C>T (p.Ser1083=)	not provided [RCV003717123]	likely benign	17	39727384	39727384	Human		name
405082501	CV3046850	single nucleotide variant	NM_004448.4(ERBB2):c.299G>A (p.Arg100Gln)	not provided [RCV003717241]	uncertain significance	17	39708394	39708394	Human		name
405137894	CV3048647	single nucleotide variant	NM_004448.4(ERBB2):c.469C>T (p.Arg157Trp)	not provided [RCV003725390]	uncertain significance	17	39709347	39709347	Human		name
405092003	CV3054647	single nucleotide variant	NM_004448.4(ERBB2):c.382C>G (p.Pro128Ala)	not provided [RCV003717885]	uncertain significance	17	39708477	39708477	Human		name
405094948	CV3054694	single nucleotide variant	NM_004448.4(ERBB2):c.457G>C (p.Val153Leu)	not provided [RCV003717913]	uncertain significance	17	39709335	39709335	Human		name
405254735	CV3055464	single nucleotide variant	NM_004448.4(ERBB2):c.940G>A (p.Val314Ile)	not provided [RCV003723062]	uncertain significance	17	39711966	39711966	Human		name
405220710	CV3059987	single nucleotide variant	NM_004448.4(ERBB2):c.3612C>T (p.Ala1204=)	not provided [RCV003733263]	likely benign	17	39727888	39727888	Human		name
12845292	CV363017	single nucleotide variant	NM_004448.4(ERBB2):c.926G>A (p.Gly309Glu)	Malignant tumor of urinary bladder [RCV003332168]	pathogenic\|likely pathogenic	17	39711952	39711952	Human	2	name
12834340	CV363067	single nucleotide variant	NM_004448.4(ERBB2):c.929C>A (p.Ser310Tyr)	not provided [RCV001311879]	pathogenic\|likely pathogenic	17	39711955	39711955	Human		name
12834324	CV363068	single nucleotide variant	NM_004448.4(ERBB2):c.929C>T (p.Ser310Phe)	Breast neoplasm [RCV000434976]\|Gastric adenocarcinoma [RCV000443823]\|Lung adenocarcinoma [RCV000426026]\|Neoplasm [RCV000442810]\|Neoplasm of the large intestine [RCV000432337]\|Neoplasm of uterine cervix [RCV000441701]\|Ovarian serous cystadenocarcinoma [RCV000417717]\|Squamous cell carcinoma of the hea ... (more) d and neck [RCV000426903]\|Squamous cell carcinoma of the skin [RCV000433436]\|Transitional cell carcinoma of the bladder [RCV000422702]	likely pathogenic	17	39711955	39711955	Human	7	name
12848726	CV363084	single nucleotide variant	NM_004448.4(ERBB2):c.926G>C (p.Gly309Ala)	Breast neoplasm [RCV000428908]	likely pathogenic	17	39711952	39711952	Human	1	name
597769157	CV3708989	single nucleotide variant	NM_004448.4(ERBB2):c.647C>T (p.Thr216Met)	Glioma susceptibility 1 [RCV005020201]	uncertain significance	17	39710089	39710089	Human	4	name
597769162	CV3708990	single nucleotide variant	NM_004448.4(ERBB2):c.655G>C (p.Val219Leu)	Glioma susceptibility 1 [RCV005020202]	uncertain significance	17	39710097	39710097	Human	4	name
597769175	CV3708991	single nucleotide variant	NM_004448.4(ERBB2):c.818C>T (p.Thr273Ile)	Glioma susceptibility 1 [RCV005020204]	uncertain significance	17	39710398	39710398	Human	4	name
597882551	CV3744988	single nucleotide variant	NM_004448.4(ERBB2):c.561C>A (p.Asn187Lys)	not provided [RCV005070013]	uncertain significance	17	39709439	39709439	Human		name
597971369	CV3750707	single nucleotide variant	NM_004448.4(ERBB2):c.868A>G (p.Thr290Ala)	not provided [RCV005084451]\|not specified [RCV005325983]	uncertain significance	17	39710448	39710448	Human		name
597952478	CV3843784	single nucleotide variant	NM_004448.4(ERBB2):c.3402C>T (p.Ser1134=)	not provided [RCV005190646]	likely benign	17	39727537	39727537	Human		name
597874821	CV3846401	single nucleotide variant	NM_004448.4(ERBB2):c.727G>A (p.Gly243Ser)	not provided [RCV005177284]	uncertain significance	17	39710169	39710169	Human		name
597964924	CV3848179	single nucleotide variant	NM_004448.4(ERBB2):c.579C>G (p.His193Gln)	not provided [RCV005194059]	uncertain significance	17	39709817	39709817	Human		name
597858364	CV3850193	single nucleotide variant	NM_004448.4(ERBB2):c.3363C>T (p.Pro1121=)	not provided [RCV005195526]	likely benign	17	39727498	39727498	Human		name
598170020	CV3961650	single nucleotide variant	NM_004448.4(ERBB2):c.605C>A (p.Ser202Tyr)	not specified [RCV005330606]	uncertain significance	17	39709843	39709843	Human		name
617152288	CV4020668	single nucleotide variant	NM_004448.4(ERBB2):c.3165C>T (p.Gly1055=)	not provided [RCV005427925]	likely benign	17	39727300	39727300	Human		name
13531605	CV512276	single nucleotide variant	NM_004448.4(ERBB2):c.307C>T (p.Arg103Ter)	Inborn genetic diseases [RCV000623480]	uncertain significance	17	39708402	39708402	Human	1	name
8607823	CV54153	deletion	NM_004448.4(ERBB2):c.2320del (p.Met774fs)	Non-small cell lung carcinoma [RCV000038125]	likely pathogenic	17	39724738	39724738	Human	2	name
15162220	CV704114	single nucleotide variant	NM_004448.4(ERBB2):c.3078C>T (p.Pro1026=)	not provided [RCV000947815]	benign	17	39726922	39726922	Human		name
15098136	CV727137	single nucleotide variant	NM_004448.4(ERBB2):c.3549C>T (p.Asp1183=)	not provided [RCV000891665]	likely benign	17	39727825	39727825	Human		name
15109434	CV727138	single nucleotide variant	NM_004448.4(ERBB2):c.3705C>T (p.Ser1235=)	not provided [RCV000893863]	benign	17	39727981	39727981	Human		name
15195433	CV755813	single nucleotide variant	NM_004448.4(ERBB2):c.3360G>A (p.Leu1120=)	not provided [RCV000911416]	likely benign	17	39727495	39727495	Human		name
15097551	CV755814	single nucleotide variant	NM_004448.4(ERBB2):c.3630T>C (p.Pro1210=)	not provided [RCV000914035]	likely benign	17	39727906	39727906	Human		name
26904538	CV845255	single nucleotide variant	NM_004448.4(ERBB2):c.365C>T (p.Pro122Leu)	not provided [RCV001070855]	uncertain significance	17	39708460	39708460	Human		name
26914217	CV845256	single nucleotide variant	NM_004448.4(ERBB2):c.470G>A (p.Arg157Gln)	not provided [RCV001037196]	uncertain significance	17	39709348	39709348	Human		name
26913861	CV845257	single nucleotide variant	NM_004448.4(ERBB2):c.593T>C (p.Met198Thr)	not provided [RCV001036593]\|not specified [RCV004619480]	uncertain significance	17	39709831	39709831	Human		name
38486683	CV937904	single nucleotide variant	NM_004448.4(ERBB2):c.907T>C (p.Tyr303His)	not provided [RCV001209000]	uncertain significance	17	39711933	39711933	Human		name
126729508	CV985877	deletion	NM_004448.4(ERBB2):c.1610del (p.Gly537fs)	Colorectal cancer [RCV001293826]	pathogenic	17	39716394	39716394	Human	2	name
126730873	CV997525	single nucleotide variant	NM_004448.4(ERBB2):c.641G>T (p.Ser214Ile)	not provided [RCV001303806]	uncertain significance	17	39709879	39709879	Human		name
126743927	CV997526	single nucleotide variant	NM_004448.4(ERBB2):c.688C>T (p.Pro230Ser)	not provided [RCV001296263]	uncertain significance	17	39710130	39710130	Human		name
126750464	CV997527	single nucleotide variant	NM_004448.4(ERBB2):c.856G>C (p.Glu286Gln)	not provided [RCV001297324]	uncertain significance	17	39710436	39710436	Human		name
126747613	CV1033256	single nucleotide variant	NM_004448.4(ERBB2):c.1138A>G (p.Ser380Gly)	not provided [RCV001337500]\|not specified [RCV004035836]	uncertain significance	17	39712438	39712438	Human		name
126765988	CV1033257	single nucleotide variant	NM_004448.4(ERBB2):c.1990G>T (p.Val664Phe)	not provided [RCV001342249]	uncertain significance	17	39723362	39723362	Human		name
126912385	CV1038523	single nucleotide variant	NM_004448.4(ERBB2):c.1607G>A (p.Arg536Gln)	not provided [RCV001358075]	uncertain significance	17	39716394	39716394	Human		name
126916955	CV1050222	single nucleotide variant	NM_004448.4(ERBB2):c.1366C>T (p.Arg456Cys)	not provided [RCV001360885]	uncertain significance	17	39715792	39715792	Human		name
126913258	CV1050224	single nucleotide variant	NM_004448.4(ERBB2):c.2431C>T (p.Arg811Trp)	not provided [RCV001370035]	uncertain significance	17	39724849	39724849	Human		name
127336819	CV1126189	single nucleotide variant	NM_004448.4(ERBB2):c.2786G>A (p.Arg929Gln)	not provided [RCV001475240]	likely benign	17	39725767	39725767	Human		name
150408683	CV1178814	single nucleotide variant	NM_004448.4(ERBB2):c.2129C>T (p.Ala710Val)	Visceral neuropathy, familial, 2, autosomal recessive [RCV001548738]	pathogenic	17	39723581	39723581	Human	1	name
151845702	CV1353482	single nucleotide variant	NM_004448.4(ERBB2):c.1685C>T (p.Pro562Leu)	not provided [RCV001957301]	uncertain significance	17	39716553	39716553	Human		name
151833873	CV1364471	single nucleotide variant	NM_004448.4(ERBB2):c.1484A>C (p.His495Pro)	not provided [RCV001976924]	uncertain significance	17	39715910	39715910	Human		name
8687357	CV137807	single nucleotide variant	NM_004448.4(ERBB2):c.1157C>A (p.Ala386Asp)	not provided [RCV000893343]\|not specified [RCV000120737]	benign\|likely benign\|not provided	17	39715294	39715294	Human	2	name
8687357	CV137807	single nucleotide variant	NM_004448.4(ERBB2):c.1157C>A (p.Ala386Asp)	not provided [RCV000893343]\|not specified [RCV000120737]	benign\|likely benign\|not provided	17	39715294	39715295	Human	2	name
8687358	CV137808	single nucleotide variant	NM_004448.4(ERBB2):c.1169C>T (p.Ala390Val)	not specified [RCV000120738]	not provided	17	39715306	39715306	Human		name
8687359	CV137809	single nucleotide variant	NM_004448.4(ERBB2):c.1231T>G (p.Tyr411Asp)	not provided [RCV003727616]\|not specified [RCV000120739]	uncertain significance\|not provided	17	39715454	39715454	Human		name
8687360	CV137810	single nucleotide variant	NM_004448.4(ERBB2):c.1466C>T (p.Pro489Leu)	Glioma susceptibility 1 [RCV005016413]\|Glioma susceptibility 1 [RCV005359144]\|not provided [RCV001048437]\|not specified [RCV000120740]	uncertain significance\|not provided	17	39715892	39715892	Human	4	name
8687361	CV137811	single nucleotide variant	NM_004448.4(ERBB2):c.1356G>T (p.Trp452Cys)	not provided [RCV000962496]\|not specified [RCV000120741]	benign\|not provided	17	39715782	39715782	Human		name
8687362	CV137812	single nucleotide variant	NM_004448.4(ERBB2):c.1793C>A (p.Ala598Asp)	Glioma susceptibility 1 [RCV005016414]\|not provided [RCV001302321]\|not specified [RCV000120742]	uncertain significance\|not provided	17	39717375	39717375	Human	4	name
8687366	CV137816	single nucleotide variant	NM_004448.4(ERBB2):c.2440C>T (p.Arg814Cys)	not specified [RCV000120748]	not provided	17	39724858	39724858	Human		name
8687367	CV137817	single nucleotide variant	NM_004448.4(ERBB2):c.2790G>T (p.Glu930Asp)	Myelodysplastic syndrome [RCV003485540]\|not provided [RCV001515034]\|not specified [RCV000120749]	benign\|likely benign\|not provided	17	39725771	39725771	Human	2	name
151880575	CV1384653	single nucleotide variant	NM_004448.4(ERBB2):c.1453C>G (p.Leu485Val)	not provided [RCV001982481]	uncertain significance	17	39715879	39715879	Human		name
151878404	CV1387232	single nucleotide variant	NM_004448.4(ERBB2):c.1436C>T (p.Thr479Met)	not provided [RCV001940683]	uncertain significance	17	39715862	39715862	Human		name
151821803	CV1387426	single nucleotide variant	NM_004448.4(ERBB2):c.2882T>C (p.Ile961Thr)	not provided [RCV001992849]	uncertain significance	17	39726571	39726571	Human		name
151839257	CV1391172	single nucleotide variant	NM_004448.4(ERBB2):c.2542G>A (p.Ala848Thr)	not provided [RCV001977488]	uncertain significance	17	39725097	39725097	Human		name
151790907	CV1393169	single nucleotide variant	NM_004448.4(ERBB2):c.1193A>G (p.Gln398Arg)	not provided [RCV001931406]	uncertain significance	17	39715330	39715330	Human		name
151825651	CV1396056	single nucleotide variant	NM_004448.4(ERBB2):c.1796G>A (p.Arg599His)	not provided [RCV001934563]	uncertain significance	17	39717378	39717378	Human		name
151768893	CV1410526	single nucleotide variant	NM_004448.4(ERBB2):c.2619C>G (p.Asp873Glu)	not provided [RCV001988050]	uncertain significance	17	39725174	39725174	Human		name
151881580	CV1413857	single nucleotide variant	NM_004448.4(ERBB2):c.2738G>A (p.Trp913Ter)	not provided [RCV002020254]	uncertain significance	17	39725719	39725719	Human		name
151773877	CV1424138	single nucleotide variant	NM_004448.4(ERBB2):c.1300C>T (p.Arg434Ter)	not provided [RCV002045505]	uncertain significance	17	39715523	39715523	Human		name
151773803	CV1427856	single nucleotide variant	NM_004448.4(ERBB2):c.1267A>G (p.Ser423Gly)	not provided [RCV001915234]	uncertain significance	17	39715490	39715490	Human		name
151745506	CV1428166	single nucleotide variant	NM_004448.4(ERBB2):c.1807G>A (p.Gly603Ser)	not provided [RCV001926913]	uncertain significance	17	39717389	39717389	Human		name
151827457	CV1435381	single nucleotide variant	NM_004448.4(ERBB2):c.1133C>T (p.Pro378Leu)	not provided [RCV001955344]	uncertain significance	17	39712433	39712433	Human		name
151774161	CV1440484	single nucleotide variant	NM_004448.4(ERBB2):c.1318G>A (p.Ala440Thr)	not provided [RCV001896633]	uncertain significance	17	39715744	39715744	Human		name
151805344	CV1440530	single nucleotide variant	NM_004448.4(ERBB2):c.2479A>C (p.Met827Leu)	not provided [RCV001932686]	uncertain significance	17	39724897	39724897	Human		name
151804968	CV1444253	single nucleotide variant	NM_004448.4(ERBB2):c.1459C>T (p.Arg487Trp)	not provided [RCV001932654]	uncertain significance	17	39715885	39715885	Human		name
151715993	CV1448415	single nucleotide variant	NM_004448.4(ERBB2):c.1597C>A (p.Gln533Lys)	not provided [RCV001965232]	uncertain significance	17	39716384	39716384	Human		name
151850676	CV1450441	single nucleotide variant	NM_004448.4(ERBB2):c.2268G>T (p.Arg756Ser)	Colorectal cancer [RCV005429196]\|not provided [RCV001922738]\|not specified [RCV005330991]	pathogenic\|uncertain significance\|low penetrance	17	39723971	39723971	Human	2	name
151876594	CV1460062	single nucleotide variant	NM_004448.4(ERBB2):c.2824C>T (p.Pro942Ser)	not provided [RCV002036330]	uncertain significance	17	39725805	39725805	Human		name
151818477	CV1464008	single nucleotide variant	NM_004448.4(ERBB2):c.1757C>T (p.Ala586Val)	not provided [RCV001933910]	uncertain significance	17	39717339	39717339	Human		name
151754282	CV1467579	single nucleotide variant	NM_004448.4(ERBB2):c.1550G>C (p.Arg517Pro)	not provided [RCV001948463]	uncertain significance	17	39716337	39716337	Human		name
151837909	CV1469956	single nucleotide variant	NM_004448.4(ERBB2):c.1411A>G (p.Asn471Asp)	not provided [RCV001881000]	uncertain significance	17	39715837	39715837	Human		name
151717241	CV1472941	single nucleotide variant	NM_004448.4(ERBB2):c.1096G>C (p.Gly366Arg)	not provided [RCV002039515]	uncertain significance	17	39712396	39712396	Human		name
151775402	CV1478644	single nucleotide variant	NM_004448.4(ERBB2):c.2996C>T (p.Pro999Leu)	not provided [RCV002045644]	uncertain significance	17	39726840	39726840	Human		name
151748236	CV1478791	single nucleotide variant	NM_004448.4(ERBB2):c.2424C>A (p.Asp808Glu)	not provided [RCV002023086]	uncertain significance	17	39724842	39724842	Human		name
151847061	CV1483915	single nucleotide variant	NM_004448.4(ERBB2):c.1837A>G (p.Ile613Val)	not provided [RCV001903574]	uncertain significance	17	39717419	39717419	Human		name
151876192	CV1484232	single nucleotide variant	NM_004448.4(ERBB2):c.1409A>G (p.His470Arg)	Glioma susceptibility 1 [RCV005016877]\|not provided [RCV001981931]	uncertain significance	17	39715835	39715835	Human	4	name
151791391	CV1486221	single nucleotide variant	NM_004448.4(ERBB2):c.2686C>G (p.Arg896Gly)	not provided [RCV002047145]	uncertain significance	17	39725363	39725363	Human		name
151835422	CV1486748	single nucleotide variant	NM_004448.4(ERBB2):c.1056G>C (p.Glu352Asp)	not provided [RCV001935502]	uncertain significance	17	39712356	39712356	Human		name
151832221	CV1487958	single nucleotide variant	NM_004448.4(ERBB2):c.2843C>T (p.Thr948Ile)	not provided [RCV001955787]	uncertain significance	17	39725824	39725824	Human		name
151873353	CV1488023	single nucleotide variant	NM_004448.4(ERBB2):c.1546G>A (p.Ala516Thr)	not provided [RCV001981589]	uncertain significance	17	39716333	39716333	Human		name
151875328	CV1490902	single nucleotide variant	NM_004448.4(ERBB2):c.1844A>G (p.Lys615Arg)	not provided [RCV001981825]	uncertain significance	17	39717426	39717426	Human		name
151783764	CV1500561	single nucleotide variant	NM_004448.4(ERBB2):c.1928C>G (p.Pro643Arg)	not provided [RCV001972323]	uncertain significance	17	39719816	39719816	Human		name
151752889	CV1508599	single nucleotide variant	NM_004448.4(ERBB2):c.1874C>T (p.Pro625Leu)	not provided [RCV001986476]	uncertain significance	17	39717456	39717456	Human		name
151842598	CV1511352	single nucleotide variant	NM_004448.4(ERBB2):c.2051A>G (p.Lys684Arg)	not provided [RCV001994937]	uncertain significance	17	39723423	39723423	Human		name
151889900	CV1514404	single nucleotide variant	NM_004448.4(ERBB2):c.2833C>G (p.Pro945Ala)	not provided [RCV001963520]	uncertain significance	17	39725814	39725814	Human		name
151729426	CV1515416	single nucleotide variant	NM_004448.4(ERBB2):c.2807A>G (p.Glu936Gly)	not provided [RCV002041039]	uncertain significance	17	39725788	39725788	Human		name
9686939	CV171593	single nucleotide variant	NM_004448.4(ERBB2):c.2706G>C (p.Gln902His)	Prostate cancer [RCV000149158]	uncertain significance	17	39725383	39725383	Human	2	name
9691630	CV176494	single nucleotide variant	NM_004448.4(ERBB2):c.2327G>T (p.Gly776Val)	not specified [RCV000150654]	not provided	17	39724745	39724745	Human		name
155696305	CV1778577	single nucleotide variant	NM_004448.4(ERBB2):c.2296G>A (p.Glu766Lys)	not provided [RCV002299647]	uncertain significance	17	39723999	39723999	Human		name
155748925	CV1778947	single nucleotide variant	NM_004448.4(ERBB2):c.1123G>A (p.Ala375Thr)	not provided [RCV002304068]	uncertain significance	17	39712423	39712423	Human		name
156390157	CV1869777	single nucleotide variant	NM_004448.4(ERBB2):c.1415C>T (p.Thr472Ile)	not provided [RCV003067931]	uncertain significance	17	39715841	39715841	Human		name
156227937	CV1896520	single nucleotide variant	NM_004448.4(ERBB2):c.2447G>A (p.Arg816His)	not provided [RCV003085250]	uncertain significance	17	39724865	39724865	Human		name
156313860	CV1896685	single nucleotide variant	NM_004448.4(ERBB2):c.1270G>A (p.Val424Ile)	Glioma susceptibility 1 [RCV005021571]\|not provided [RCV003088603]	uncertain significance	17	39715493	39715493	Human	4	name
155982870	CV1896885	single nucleotide variant	NM_004448.4(ERBB2):c.1429G>A (p.Val477Met)	not provided [RCV003097471]	uncertain significance	17	39715855	39715855	Human		name
156220436	CV1899739	single nucleotide variant	NM_004448.4(ERBB2):c.1621G>A (p.Val541Met)	not provided [RCV003084973]	uncertain significance	17	39716408	39716408	Human		name
156163271	CV1903194	single nucleotide variant	NM_004448.4(ERBB2):c.1172C>T (p.Pro391Leu)	not provided [RCV003082980]	uncertain significance	17	39715309	39715309	Human		name
156030026	CV1903352	single nucleotide variant	NM_004448.4(ERBB2):c.1093G>A (p.Ala365Thr)	not provided [RCV003100609]	uncertain significance	17	39712393	39712393	Human		name
156345303	CV1907836	single nucleotide variant	NM_004448.4(ERBB2):c.1507G>A (p.Glu503Lys)	not provided [RCV003090601]	uncertain significance	17	39715933	39715933	Human		name
156076403	CV1912424	single nucleotide variant	NM_004448.4(ERBB2):c.1831A>G (p.Met611Val)	not provided [RCV002591433]	uncertain significance	17	39717413	39717413	Human		name
156300416	CV1916056	single nucleotide variant	NM_004448.4(ERBB2):c.1933G>A (p.Glu645Lys)	not provided [RCV002599143]	uncertain significance	17	39719821	39719821	Human		name
156200218	CV1928939	single nucleotide variant	NM_004448.4(ERBB2):c.1028A>G (p.Tyr343Cys)	not provided [RCV002643607]	uncertain significance	17	39712328	39712328	Human		name
156449391	CV1941321	single nucleotide variant	NM_004448.4(ERBB2):c.2048G>C (p.Arg683Pro)	not provided [RCV003121512]	uncertain significance	17	39723420	39723420	Human		name
156441726	CV1941403	single nucleotide variant	NM_004448.4(ERBB2):c.2690G>A (p.Arg897Gln)	not provided [RCV003112057]	uncertain significance	17	39725367	39725367	Human		name
156110051	CV2008583	single nucleotide variant	NM_004448.4(ERBB2):c.1509G>C (p.Glu503Asp)	not provided [RCV002695633]	uncertain significance	17	39715935	39715935	Human		name
156005306	CV2045980	single nucleotide variant	NM_004448.4(ERBB2):c.2932C>T (p.Arg978Cys)	not provided [RCV002794820]	uncertain significance	17	39726621	39726621	Human		name
156007802	CV2046184	single nucleotide variant	NM_004448.4(ERBB2):c.1295G>A (p.Arg432Gln)	not provided [RCV002756516]	uncertain significance	17	39715518	39715518	Human		name
156351927	CV2065862	single nucleotide variant	NM_004448.4(ERBB2):c.1238C>G (p.Ser413Ter)	not provided [RCV002811849]	uncertain significance	17	39715461	39715461	Human		name
156011083	CV2075596	single nucleotide variant	NM_004448.4(ERBB2):c.1319C>T (p.Ala440Val)	not provided [RCV002843877]	uncertain significance	17	39715745	39715745	Human		name
155932982	CV2142276	single nucleotide variant	NM_004448.4(ERBB2):c.1736C>T (p.Pro579Leu)	not provided [RCV002993520]	uncertain significance	17	39716604	39716604	Human		name
155955081	CV2143924	single nucleotide variant	NM_004448.4(ERBB2):c.1826C>T (p.Ser609Phe)	not provided [RCV002994849]	uncertain significance	17	39717408	39717408	Human		name
156202003	CV2150086	single nucleotide variant	NM_004448.4(ERBB2):c.1556A>G (p.His519Arg)	Glioma susceptibility 1 [RCV005019561]\|not provided [RCV003006358]	uncertain significance	17	39716343	39716343	Human	4	name
155946092	CV2265972	single nucleotide variant	NM_004448.4(ERBB2):c.1660T>A (p.Tyr554Asn)	not specified [RCV004126805]	uncertain significance	17	39716528	39716528	Human		name
156180085	CV2288066	single nucleotide variant	NM_004448.4(ERBB2):c.2156A>T (p.Glu719Val)	not specified [RCV004147819]	uncertain significance	17	39723608	39723608	Human		name
329367638	CV2456964	single nucleotide variant	NM_004448.4(ERBB2):c.2405C>T (p.Pro802Leu)	not specified [RCV004270905]	uncertain significance	17	39724823	39724823	Human		name
401735454	CV2699272	single nucleotide variant	NM_004448.4(ERBB2):c.1765C>G (p.His589Asp)	not specified [RCV004305539]	uncertain significance	17	39717347	39717347	Human		name
401724417	CV2738064	duplication	NM_004448.4(ERBB2):c.3694dup (p.Ala1232fs)	Neuroepithelial tumor, PATZ1 fusion-positive [RCV003315274]	uncertain significance	17	39727964	39727965	Human		name
401873758	CV2749805	single nucleotide variant	NM_004448.4(ERBB2):c.2089G>A (p.Val697Met)	Malignant tumor of urinary bladder [RCV003332933]	pathogenic	17	39723541	39723541	Human	2	name
401873759	CV2749806	single nucleotide variant	NM_004448.4(ERBB2):c.2515G>A (p.Val839Met)	Malignant tumor of urinary bladder [RCV003332934]	pathogenic	17	39725070	39725070	Human	2	name
401873866	CV2749862	single nucleotide variant	NM_004448.4(ERBB2):c.1958C>T (p.Ser653Phe)	Malignant tumor of urinary bladder [RCV003332990]	pathogenic	17	39723330	39723330	Human	2	name
401890248	CV2763742	single nucleotide variant	NM_004448.4(ERBB2):c.2982G>C (p.Leu994Phe)	not specified [RCV004343230]	uncertain significance	17	39726826	39726826	Human		name
405045115	CV2859883	single nucleotide variant	NM_004448.4(ERBB2):c.2770G>T (p.Asp924Tyr)	not provided [RCV003579395]	uncertain significance	17	39725751	39725751	Human		name
405075810	CV2873310	single nucleotide variant	NM_004448.4(ERBB2):c.2327G>C (p.Gly776Ala)	not provided [RCV003548806]	uncertain significance	17	39724745	39724745	Human		name
405238270	CV2881166	single nucleotide variant	NM_004448.4(ERBB2):c.1487C>T (p.Thr496Ile)	not provided [RCV003556667]	uncertain significance	17	39715913	39715913	Human		name
405049942	CV2886776	single nucleotide variant	NM_004448.4(ERBB2):c.2933G>A (p.Arg978His)	not provided [RCV003579628]	uncertain significance	17	39726622	39726622	Human		name
8563935	CV28912	single nucleotide variant	NM_004448.4(ERBB2):c.1963A>G (p.Ile655Val)	ERBB2 POLYMORPHISM [RCV000014887]\|not provided [RCV001511302]\|not specified [RCV000120744]	pathogenic\|benign\|not provided	17	39723335	39723335	Human		name , trait
8563936	CV28913	single nucleotide variant	NM_004448.4(ERBB2):c.1960A>G (p.Ile654Val)	ERBB2 POLYMORPHISM [RCV000014888]\|not provided [RCV001513234]\|not specified [RCV000120743]	benign\|likely benign\|not provided	17	39723332	39723332	Human		name , trait
8563940	CV28917	single nucleotide variant	NM_004448.4(ERBB2):c.2740G>A (p.Glu914Lys)	Glioma susceptibility 1 [RCV000014892]	pathogenic\|other	17	39725721	39725721	Human	1	name
8563941	CV28918	single nucleotide variant	NM_004448.4(ERBB2):c.2326G>A (p.Gly776Ser)	Gastric cancer [RCV000014893]	pathogenic\|likely pathogenic\|other	17	39724744	39724744	Human	2	name
8563942	CV28919	single nucleotide variant	NM_004448.4(ERBB2):c.2570A>G (p.Asn857Ser)	Ovarian neoplasm [RCV000014894]	pathogenic\|likely pathogenic\|other	17	39725125	39725125	Human	2	name
405030150	CV2926131	single nucleotide variant	NM_004448.4(ERBB2):c.1523G>A (p.Gly508Asp)	not provided [RCV003578299]	uncertain significance	17	39716310	39716310	Human		name
402506595	CV2927958	single nucleotide variant	NM_004448.4(ERBB2):c.1523G>C (p.Gly508Ala)	not provided [RCV003574519]	uncertain significance	17	39716310	39716310	Human		name
402518264	CV3002227	single nucleotide variant	NM_004448.4(ERBB2):c.2256C>G (p.Ile752Met)	not provided [RCV003690094]	uncertain significance	17	39723959	39723959	Human		name
405005715	CV3010039	single nucleotide variant	NM_004448.4(ERBB2):c.2674G>A (p.Glu892Lys)	not provided [RCV003693559]	uncertain significance	17	39725351	39725351	Human		name
405124848	CV3043452	single nucleotide variant	NM_004448.4(ERBB2):c.1397C>T (p.Ala466Val)	not provided [RCV003724269]	uncertain significance	17	39715823	39715823	Human		name
405084661	CV3043720	single nucleotide variant	NM_004448.4(ERBB2):c.1547C>T (p.Ala516Val)	not provided [RCV003717388]	uncertain significance	17	39716334	39716334	Human		name
405253496	CV3044387	single nucleotide variant	NM_004448.4(ERBB2):c.1940G>A (p.Arg647Lys)	not provided [RCV003722477]	uncertain significance	17	39719828	39719828	Human		name
405218960	CV3049144	single nucleotide variant	NM_004448.4(ERBB2):c.1282C>G (p.Leu428Val)	not provided [RCV003732968]	uncertain significance	17	39715505	39715505	Human		name
405176186	CV3049383	single nucleotide variant	NM_004448.4(ERBB2):c.1207C>A (p.Leu403Met)	not provided [RCV003728361]	uncertain significance	17	39715344	39715344	Human		name
405128551	CV3050125	duplication	NM_004448.4(ERBB2):c.3738dup (p.Glu1247fs)	not provided [RCV003724546]	uncertain significance	17	39728013	39728014	Human		name
405079725	CV3050366	single nucleotide variant	NM_004448.4(ERBB2):c.1550G>A (p.Arg517Gln)	Glioma susceptibility 1 [RCV005014890]\|not provided [RCV003717047]	uncertain significance	17	39716337	39716337	Human	4	name
405131785	CV3051181	single nucleotide variant	NM_004448.4(ERBB2):c.2614A>G (p.Ile872Val)	not provided [RCV003724891]	uncertain significance	17	39725169	39725169	Human		name
405133943	CV3051357	single nucleotide variant	NM_004448.4(ERBB2):c.2687G>A (p.Arg896His)	not provided [RCV003724993]	uncertain significance	17	39725364	39725364	Human		name
405245257	CV3051373	single nucleotide variant	NM_004448.4(ERBB2):c.1864G>A (p.Ala622Thr)	not provided [RCV003720241]	uncertain significance	17	39717446	39717446	Human		name
405202991	CV3052790	single nucleotide variant	NM_004448.4(ERBB2):c.2909G>A (p.Arg970Gln)	not provided [RCV003730973]	uncertain significance	17	39726598	39726598	Human		name
405125699	CV3053377	single nucleotide variant	NM_004448.4(ERBB2):c.1460G>A (p.Arg487Gln)	not provided [RCV003724349]	uncertain significance	17	39715886	39715886	Human		name
405253490	CV3054249	single nucleotide variant	NM_004448.4(ERBB2):c.2689C>T (p.Arg897Trp)	not provided [RCV003722552]	uncertain significance	17	39725366	39725366	Human		name
405211338	CV3059185	single nucleotide variant	NM_004448.4(ERBB2):c.2707A>C (p.Ser903Arg)	not provided [RCV003732054]	uncertain significance	17	39725384	39725384	Human		name
405179056	CV3060341	single nucleotide variant	NM_004448.4(ERBB2):c.1882A>G (p.Ile628Val)	not provided [RCV003728605]	uncertain significance	17	39717464	39717464	Human		name
405180559	CV3060611	single nucleotide variant	NM_004448.4(ERBB2):c.2398C>T (p.Leu800Phe)	not provided [RCV003728731]	uncertain significance	17	39724816	39724816	Human		name
405201595	CV3066863	single nucleotide variant	NM_004448.4(ERBB2):c.2638G>C (p.Asp880His)	not provided [RCV003730771]	uncertain significance	17	39725193	39725193	Human		name
405102947	CV3119550	single nucleotide variant	NM_004448.4(ERBB2):c.2965A>G (p.Ile989Val)	not provided [RCV003811812]	uncertain significance	17	39726654	39726654	Human		name
405120588	CV3131426	single nucleotide variant	NM_004448.4(ERBB2):c.2086C>A (p.Leu696Met)	not provided [RCV003837290]	uncertain significance	17	39723538	39723538	Human		name
405174360	CV3151872	single nucleotide variant	NM_004448.4(ERBB2):c.1858G>A (p.Glu620Lys)	not provided [RCV003858023]	uncertain significance	17	39717440	39717440	Human		name
405237449	CV3166887	single nucleotide variant	NM_004448.4(ERBB2):c.1683G>T (p.Leu561Phe)	not provided [RCV003854141]	uncertain significance	17	39716551	39716551	Human		name
405240989	CV3176850	single nucleotide variant	NM_004448.4(ERBB2):c.2492A>G (p.Lys831Arg)	not provided [RCV003867288]	uncertain significance	17	39724910	39724910	Human		name
402487996	CV3181896	single nucleotide variant	NM_004448.4(ERBB2):c.1970C>T (p.Ala657Val)	not provided [RCV003876565]	uncertain significance	17	39723342	39723342	Human		name
404986188	CV3183852	single nucleotide variant	NM_004448.4(ERBB2):c.1943C>T (p.Ala648Val)	not provided [RCV003881129]	uncertain significance	17	39719831	39719831	Human		name
12836476	CV362870	single nucleotide variant	NM_004448.4(ERBB2):c.2305G>C (p.Asp769His)	Breast neoplasm [RCV000445220]\|Carcinoma of esophagus [RCV000423455]\|Gastric adenocarcinoma [RCV000426351]\|Neoplasm of uterine cervix [RCV000444643]\|Transitional cell carcinoma of the bladder [RCV000433752]	pathogenic\|likely pathogenic	17	39724008	39724008	Human	4	name
12834379	CV362871	single nucleotide variant	NM_004448.4(ERBB2):c.2305G>T (p.Asp769Tyr)	Breast neoplasm [RCV000427352]\|Carcinoma of esophagus [RCV000437580]\|Gastric adenocarcinoma [RCV000443774]\|Neoplasm of uterine cervix [RCV000438329]\|Transitional cell carcinoma of the bladder [RCV000418272]	pathogenic\|likely pathogenic	17	39724008	39724008	Human	4	name
12835631	CV362873	single nucleotide variant	NM_004448.4(ERBB2):c.2524G>A (p.Val842Ile)	not provided [RCV001861475]	pathogenic\|likely pathogenic\|uncertain significance	17	39725079	39725079	Human		name
12848722	CV362874	single nucleotide variant	NM_004448.4(ERBB2):c.2686C>T (p.Arg896Cys)	Breast neoplasm [RCV000424169]	pathogenic	17	39725363	39725363	Human	1	name
12834292	CV362914	single nucleotide variant	NM_004448.4(ERBB2):c.2264T>C (p.Leu755Ser)	Breast neoplasm [RCV000435086]\|Gastric adenocarcinoma [RCV000435324]\|Malignant melanoma of skin [RCV000428572]\|Malignant neoplasm of body of uterus [RCV000417433]\|Neoplasm of the large intestine [RCV000427447]\|Papillary renal cell carcinoma, sporadic [RCV000418445]\|Transitional cell carcinoma of the ... (more) bladder [RCV000429126]	likely pathogenic	17	39723967	39723967	Human	5	name
12848737	CV362915	single nucleotide variant	NM_004448.4(ERBB2):c.2329G>C (p.Val777Leu)	Breast neoplasm [RCV000439788]	likely pathogenic	17	39724747	39724747	Human	1	name
12848739	CV363212	single nucleotide variant	NM_004448.4(ERBB2):c.2354T>C (p.Leu785Pro)	Breast neoplasm [RCV000442075]	likely pathogenic	17	39724772	39724772	Human	1	name
12834341	CV363222	single nucleotide variant	NM_004448.4(ERBB2):c.2264T>G (p.Leu755Trp)	Breast neoplasm [RCV000425422]\|Gastric adenocarcinoma [RCV000426066]\|Malignant melanoma of skin [RCV000435694]\|Malignant neoplasm of body of uterus [RCV000442700]\|Neoplasm of the large intestine [RCV000417866]\|Papillary renal cell carcinoma, sporadic [RCV000445218]\|Transitional cell carcinoma of the ... (more) bladder [RCV000432853]	likely pathogenic	17	39723967	39723967	Human	5	name
12834337	CV363223	single nucleotide variant	NM_004448.4(ERBB2):c.2033G>A (p.Arg678Gln)	Breast neoplasm [RCV000424585]\|Gastric adenocarcinoma [RCV000438950]\|Malignant neoplasm of body of uterus [RCV000417832]\|Neoplasm of the large intestine [RCV000437885]\|Prostate adenocarcinoma [RCV000428060]\|Transitional cell carcinoma of the bladder [RCV000420241]	likely pathogenic\|not provided	17	39723405	39723405	Human	4	name
12834459	CV363282	single nucleotide variant	NM_004448.4(ERBB2):c.2305G>A (p.Asp769Asn)	Breast neoplasm [RCV000431162]\|Carcinoma of esophagus [RCV000419212]\|Gastric adenocarcinoma [RCV000420244]\|Neoplasm of uterine cervix [RCV000441427]\|Transitional cell carcinoma of the bladder [RCV000430490]	likely pathogenic	17	39724008	39724008	Human	4	name
12835256	CV363283	single nucleotide variant	NM_004448.4(ERBB2):c.2263T>A (p.Leu755Met)	Breast neoplasm [RCV000431643]\|Gastric adenocarcinoma [RCV000439036]\|Malignant melanoma of skin [RCV000432868]\|Malignant neoplasm of body of uterus [RCV000438379]\|Neoplasm of the large intestine [RCV000422582]\|Papillary renal cell carcinoma, sporadic [RCV000421368]\|Transitional cell carcinoma of the ... (more) bladder [RCV000443340]	likely pathogenic	17	39723966	39723966	Human	5	name
12835621	CV363285	single nucleotide variant	NM_004448.4(ERBB2):c.2329G>A (p.Val777Met)	Breast neoplasm [RCV000439665]\|Gastric adenocarcinoma [RCV000422009]\|Neoplasm of the large intestine [RCV000428744]	likely pathogenic	17	39724747	39724747	Human	3	name
597804160	CV3671436	single nucleotide variant	NM_004448.4(ERBB2):c.1474G>C (p.Ala492Pro)	not specified [RCV004907555]	uncertain significance	17	39715900	39715900	Human		name
597804163	CV3671437	single nucleotide variant	NM_004448.4(ERBB2):c.1465C>T (p.Pro489Ser)	not specified [RCV004907556]	uncertain significance	17	39715891	39715891	Human		name
597769180	CV3708992	single nucleotide variant	NM_004448.4(ERBB2):c.1195G>A (p.Val399Met)	Glioma susceptibility 1 [RCV005020205]	uncertain significance	17	39715332	39715332	Human	4	name
597769194	CV3708994	single nucleotide variant	NM_004448.4(ERBB2):c.1506C>A (p.Asp502Glu)	Glioma susceptibility 1 [RCV005020207]	uncertain significance	17	39715932	39715932	Human	4	name
597769204	CV3708995	single nucleotide variant	NM_004448.4(ERBB2):c.1894C>T (p.His632Tyr)	Glioma susceptibility 1 [RCV005020209]	uncertain significance	17	39717476	39717476	Human	4	name
597769217	CV3708997	single nucleotide variant	NM_004448.4(ERBB2):c.2458C>G (p.Gln820Glu)	Glioma susceptibility 1 [RCV005020211]	uncertain significance	17	39724876	39724876	Human	4	name
597908721	CV3739035	single nucleotide variant	NM_004448.4(ERBB2):c.1287A>C (p.Gln429His)	not provided [RCV005073270]	uncertain significance	17	39715510	39715510	Human		name
597899719	CV3740969	single nucleotide variant	NM_004448.4(ERBB2):c.1828T>A (p.Tyr610Asn)	not provided [RCV005072132]	uncertain significance	17	39717410	39717410	Human		name
597882542	CV3744989	single nucleotide variant	NM_004448.4(ERBB2):c.1064C>T (p.Ala355Val)	not provided [RCV005070014]	uncertain significance	17	39712364	39712364	Human		name
597965779	CV3751200	single nucleotide variant	NM_004448.4(ERBB2):c.2172G>C (p.Lys724Asn)	not provided [RCV005082762]	uncertain significance	17	39723624	39723624	Human		name
597834691	CV3760790	single nucleotide variant	NM_004448.4(ERBB2):c.2519G>A (p.Arg840Gln)	not provided [RCV005085341]	uncertain significance	17	39725074	39725074	Human		name
597952346	CV3765623	single nucleotide variant	NM_004448.4(ERBB2):c.2641G>C (p.Gly881Arg)	not provided [RCV005121267]	uncertain significance	17	39725196	39725196	Human		name
597906369	CV3773068	single nucleotide variant	NM_004448.4(ERBB2):c.1816C>T (p.Pro606Ser)	not provided [RCV005113132]	uncertain significance	17	39717398	39717398	Human		name
597921575	CV3774978	single nucleotide variant	NM_004448.4(ERBB2):c.1496G>A (p.Arg499Gln)	not provided [RCV005115324]	uncertain significance	17	39715922	39715922	Human		name
597969079	CV3791191	single nucleotide variant	NM_004448.4(ERBB2):c.2989G>T (p.Ala997Ser)	not provided [RCV005141223]	uncertain significance	17	39726833	39726833	Human		name
597959314	CV3797534	single nucleotide variant	NM_004448.4(ERBB2):c.1463A>C (p.Asn488Thr)	not provided [RCV005138221]	uncertain significance	17	39715889	39715889	Human		name
597880738	CV3810312	single nucleotide variant	NM_004448.4(ERBB2):c.2125C>G (p.Gln709Glu)	not provided [RCV005149773]	uncertain significance	17	39723577	39723577	Human		name
597943451	CV3812340	single nucleotide variant	NM_004448.4(ERBB2):c.1460G>T (p.Arg487Leu)	not provided [RCV005159550]	uncertain significance	17	39715886	39715886	Human		name
597853430	CV3825110	single nucleotide variant	NM_004448.4(ERBB2):c.1761T>A (p.Cys587Ter)	not provided [RCV005173958]	uncertain significance	17	39717343	39717343	Human		name
597926547	CV3836824	single nucleotide variant	NM_004448.4(ERBB2):c.1051C>T (p.Arg351Ter)	not provided [RCV005185175]	uncertain significance	17	39712351	39712351	Human		name
597960693	CV3840294	single nucleotide variant	NM_004448.4(ERBB2):c.1013G>A (p.Cys338Tyr)	not provided [RCV005192777]	uncertain significance	17	39712039	39712039	Human		name
597924670	CV3840451	single nucleotide variant	NM_004448.4(ERBB2):c.2446C>T (p.Arg816Cys)	not provided [RCV005184921]	uncertain significance	17	39724864	39724864	Human		name
597946582	CV3841687	single nucleotide variant	NM_004448.4(ERBB2):c.1442C>T (p.Pro481Leu)	not provided [RCV005189121]	uncertain significance	17	39715868	39715868	Human		name
597960193	CV3843583	single nucleotide variant	NM_004448.4(ERBB2):c.1930G>A (p.Ala644Thr)	not provided [RCV005192620]\|not specified [RCV005326047]	uncertain significance	17	39719818	39719818	Human		name
597942309	CV3847223	single nucleotide variant	NM_004448.4(ERBB2):c.1949C>T (p.Pro650Leu)	not provided [RCV005188143]	uncertain significance	17	39723321	39723321	Human		name
597943143	CV3847425	single nucleotide variant	NM_004448.4(ERBB2):c.1367G>A (p.Arg456His)	not provided [RCV005188344]	uncertain significance	17	39715793	39715793	Human		name
597951742	CV3847453	single nucleotide variant	NM_004448.4(ERBB2):c.1981A>G (p.Ile661Val)	not provided [RCV005190435]	uncertain significance	17	39723353	39723353	Human		name
597894725	CV3857233	single nucleotide variant	NM_004448.4(ERBB2):c.1979G>A (p.Gly660Asp)	not provided [RCV005201097]	uncertain significance	17	39723351	39723351	Human		name
597889007	CV3859590	single nucleotide variant	NM_004448.4(ERBB2):c.1859A>G (p.Glu620Gly)	not provided [RCV005200246]	uncertain significance	17	39717441	39717441	Human		name
13207938	CV424554	single nucleotide variant	NM_004448.4(ERBB2):c.2606T>G (p.Leu869Arg)	Lung adenocarcinoma [RCV000491283]	pathogenic	17	39725161	39725161	Human	2	name
8607828	CV54158	single nucleotide variant	NM_004448.4(ERBB2):c.2329G>T (p.Val777Leu)	not specified [RCV000038130]	pathogenic\|likely pathogenic\|uncertain significance	17	39724747	39724747	Human		name
8607831	CV54161	single nucleotide variant	NM_004448.4(ERBB2):c.2443G>A (p.Gly815Arg)	not provided [RCV002054687]\|not specified [RCV000038133]	pathogenic\|benign\|likely benign	17	39724861	39724861	Human		name
8627981	CV83125	single nucleotide variant	NM_004448.4(ERBB2):c.1471C>T (p.Gln491Ter)	not provided [RCV003662179]	uncertain significance\|not provided	17	39715897	39715897	Human		name
26889350	CV845258	single nucleotide variant	NM_004448.4(ERBB2):c.1495C>T (p.Arg499Trp)	not provided [RCV001058128]	uncertain significance	17	39715921	39715921	Human		name
26918248	CV845260	single nucleotide variant	NM_004448.4(ERBB2):c.2048G>A (p.Arg683Gln)	not provided [RCV001043290]	uncertain significance	17	39723420	39723420	Human		name
26916365	CV845261	single nucleotide variant	NM_004448.4(ERBB2):c.2317G>A (p.Val773Met)	not provided [RCV001040267]	uncertain significance	17	39724735	39724735	Human		name
38488832	CV949894	single nucleotide variant	NM_004448.4(ERBB2):c.1294C>T (p.Arg432Trp)	Visceral neuropathy, familial, 2, autosomal recessive [RCV004727026]\|not provided [RCV001238170]	likely benign\|uncertain significance	17	39715517	39715517	Human	1	name
38489754	CV949895	single nucleotide variant	NM_004448.4(ERBB2):c.1489G>A (p.Ala497Thr)	not provided [RCV001238548]	uncertain significance	17	39715915	39715915	Human		name
38495843	CV949896	single nucleotide variant	NM_004448.4(ERBB2):c.1772A>T (p.Lys591Met)	Glioma susceptibility 1 [RCV005014262]\|not provided [RCV001225993]	uncertain significance	17	39717354	39717354	Human	4	name
38459756	CV958096	single nucleotide variant	NM_004448.4(ERBB2):c.1385G>A (p.Gly462Asp)	not provided [RCV001246618]	uncertain significance	17	39715811	39715811	Human		name
38491801	CV958097	single nucleotide variant	NM_004448.4(ERBB2):c.1567C>T (p.Pro523Ser)	not provided [RCV001239675]	uncertain significance	17	39716354	39716354	Human		name
126725211	CV1033258	single nucleotide variant	NM_004448.4(ERBB2):c.3086G>C (p.Gly1029Ala)	not provided [RCV001348080]	uncertain significance	17	39726930	39726930	Human		name
126770560	CV1033259	single nucleotide variant	NM_004448.4(ERBB2):c.3308C>T (p.Thr1103Ile)	not provided [RCV001344544]\|not specified [RCV004619654]	uncertain significance	17	39727443	39727443	Human		name
126746099	CV1033260	single nucleotide variant	NM_004448.4(ERBB2):c.3332G>A (p.Arg1111Gln)	not provided [RCV001337283]	uncertain significance	17	39727467	39727467	Human		name
126771200	CV1033261	single nucleotide variant	NM_004448.4(ERBB2):c.3430G>C (p.Asp1144His)	not provided [RCV001344903]	uncertain significance	17	39727706	39727706	Human		name
126762978	CV1033262	single nucleotide variant	NM_004448.4(ERBB2):c.3662A>G (p.Tyr1221Cys)	not provided [RCV001341129]	uncertain significance	17	39727938	39727938	Human		name
126914219	CV1050226	single nucleotide variant	NM_004448.4(ERBB2):c.3436C>T (p.Arg1146Trp)	Visceral neuropathy, familial, 2, autosomal recessive [RCV004728685]\|not provided [RCV001370394]	likely benign\|uncertain significance	17	39727712	39727712	Human	1	name
127302560	CV1157961	single nucleotide variant	NM_004448.4(ERBB2):c.3403C>T (p.Pro1135Ser)	not provided [RCV001515106]	benign	17	39727538	39727538	Human		name
150543201	CV1309359	single nucleotide variant	NM_004448.4(ERBB2):c.3149C>T (p.Ser1050Leu)	not provided [RCV001868766]	uncertain significance	17	39726993	39726993	Human		name
151851849	CV1349745	single nucleotide variant	NM_004448.4(ERBB2):c.3550G>A (p.Val1184Ile)	not provided [RCV001958101]	uncertain significance	17	39727826	39727826	Human		name
151862342	CV1353453	single nucleotide variant	NM_004448.4(ERBB2):c.3166G>A (p.Gly1056Ser)	Glioma susceptibility 1 [RCV005016868]\|not provided [RCV001924159]	uncertain significance	17	39727301	39727301	Human	4	name
8688925	CV136712	single nucleotide variant	NM_004448.4(ERBB2):c.3146G>A (p.Ser1049Asn)	Familial cancer of breast [RCV000119365]	not provided	17	39726990	39726990	Human		name
151772422	CV1368425	single nucleotide variant	NM_004448.4(ERBB2):c.3689G>C (p.Arg1230Pro)	not provided [RCV001950292]	uncertain significance	17	39727965	39727965	Human		name
151719028	CV1373612	single nucleotide variant	NM_004448.4(ERBB2):c.3757G>A (p.Val1253Met)	not provided [RCV001890791]	uncertain significance	17	39728033	39728033	Human		name
8687368	CV137818	single nucleotide variant	NM_004448.4(ERBB2):c.3182T>C (p.Leu1061Pro)	Glioma susceptibility 1 [RCV005400424]\|not provided [RCV001364689]\|not specified [RCV000120750]	uncertain significance\|not provided	17	39727317	39727317	Human	4	name
8687369	CV137819	single nucleotide variant	NM_004448.4(ERBB2):c.3427C>A (p.Pro1143Thr)	not provided [RCV003718116]\|not specified [RCV000120751]	uncertain significance\|not provided	17	39727703	39727703	Human		name
8687370	CV137820	single nucleotide variant	NM_004448.4(ERBB2):c.3428C>T (p.Pro1143Leu)	not provided [RCV002515853]\|not specified [RCV000120752]	uncertain significance\|not provided	17	39727704	39727704	Human		name
8687371	CV137821	single nucleotide variant	NM_004448.4(ERBB2):c.3508C>G (p.Pro1170Ala)	not provided [RCV001520147]\|not specified [RCV000120753]	benign\|not provided	17	39727784	39727784	Human		name
8687372	CV137822	single nucleotide variant	NM_004448.4(ERBB2):c.3620C>T (p.Pro1207Leu)	not provided [RCV001854611]\|not specified [RCV000120754]	uncertain significance\|not provided	17	39727896	39727896	Human		name
8687373	CV137823	single nucleotide variant	NM_004448.4(ERBB2):c.3647C>A (p.Ala1216Asp)	not provided [RCV000881822]\|not specified [RCV000120755]	benign\|likely benign\|not provided	17	39727923	39727923	Human		name
8687374	CV137824	single nucleotide variant	NM_004448.4(ERBB2):c.3482G>A (p.Arg1161Gln)	not provided [RCV001512300]\|not specified [RCV000120756]	benign\|not provided	17	39727758	39727758	Human		name
8687375	CV137825	single nucleotide variant	NM_004448.4(ERBB2):c.3689G>T (p.Arg1230Leu)	not provided [RCV001854612]\|not specified [RCV000120757]	uncertain significance\|not provided	17	39727965	39727965	Human		name
151727016	CV1409821	single nucleotide variant	NM_004448.4(ERBB2):c.3034G>A (p.Asp1012Asn)	not provided [RCV001910478]	uncertain significance	17	39726878	39726878	Human		name
151745789	CV1428211	single nucleotide variant	NM_004448.4(ERBB2):c.3337A>G (p.Ser1113Gly)	not provided [RCV001926948]	uncertain significance	17	39727472	39727472	Human		name
151742364	CV1431612	single nucleotide variant	NM_004448.4(ERBB2):c.3031G>A (p.Asp1011Asn)	not provided [RCV001926588]	uncertain significance	17	39726875	39726875	Human		name
151745558	CV1432836	single nucleotide variant	NM_004448.4(ERBB2):c.3305C>T (p.Pro1102Leu)	not provided [RCV001985688]	uncertain significance	17	39727440	39727440	Human		name
151726245	CV1433457	single nucleotide variant	NM_004448.4(ERBB2):c.3382G>A (p.Val1128Ile)	not provided [RCV001983714]	uncertain significance	17	39727517	39727517	Human		name
151788869	CV1434308	single nucleotide variant	NM_004448.4(ERBB2):c.3331C>T (p.Arg1111Trp)	not provided [RCV001876316]	uncertain significance	17	39727466	39727466	Human		name
151828017	CV1437996	single nucleotide variant	NM_004448.4(ERBB2):c.3754G>A (p.Asp1252Asn)	not provided [RCV001920214]	uncertain significance	17	39728030	39728030	Human		name
151752907	CV1457626	single nucleotide variant	NM_004448.4(ERBB2):c.3611C>G (p.Ala1204Gly)	not provided [RCV001948329]	uncertain significance	17	39727887	39727887	Human		name
151757294	CV1459740	single nucleotide variant	NM_004448.4(ERBB2):c.3533A>G (p.Asn1178Ser)	not provided [RCV001986879]	uncertain significance	17	39727809	39727809	Human		name
151840910	CV1464195	single nucleotide variant	NM_004448.4(ERBB2):c.3688C>T (p.Arg1230Trp)	not provided [RCV001936101]	uncertain significance	17	39727964	39727964	Human		name
151865986	CV1477645	single nucleotide variant	NM_004448.4(ERBB2):c.3544A>C (p.Lys1182Gln)	not provided [RCV001939165]	uncertain significance	17	39727820	39727820	Human		name
151838813	CV1487459	single nucleotide variant	NM_004448.4(ERBB2):c.3725C>T (p.Thr1242Met)	not provided [RCV001935856]	uncertain significance	17	39728001	39728001	Human		name
151803840	CV1492098	single nucleotide variant	NM_004448.4(ERBB2):c.3202G>T (p.Glu1068Ter)	not provided [RCV002048223]	uncertain significance	17	39727337	39727337	Human		name
151734113	CV1497658	single nucleotide variant	NM_004448.4(ERBB2):c.3458G>A (p.Arg1153Gln)	not provided [RCV001984501]	uncertain significance	17	39727734	39727734	Human		name
151796694	CV1499680	single nucleotide variant	NM_004448.4(ERBB2):c.3142C>T (p.Arg1048Cys)	Glioma susceptibility 1 [RCV005016732]\|not provided [RCV001917328]	uncertain significance	17	39726986	39726986	Human	4	name
151847046	CV1513127	single nucleotide variant	NM_004448.4(ERBB2):c.3672C>G (p.Asp1224Glu)	not provided [RCV001922262]	uncertain significance	17	39727948	39727948	Human		name
156342750	CV1897022	single nucleotide variant	NM_004448.4(ERBB2):c.3190G>A (p.Glu1064Lys)	not provided [RCV003090457]	uncertain significance	17	39727325	39727325	Human		name
156267562	CV1899191	single nucleotide variant	NM_004448.4(ERBB2):c.3496A>G (p.Thr1166Ala)	not provided [RCV003086665]\|not specified [RCV004073209]	uncertain significance	17	39727772	39727772	Human		name
156286590	CV1900641	single nucleotide variant	NM_004448.4(ERBB2):c.3288G>C (p.Lys1096Asn)	Glioma susceptibility 1 [RCV005021579]\|not provided [RCV002598580]	uncertain significance	17	39727423	39727423	Human	4	name
156030094	CV1903360	single nucleotide variant	NM_004448.4(ERBB2):c.3689G>A (p.Arg1230Gln)	not provided [RCV003100612]	uncertain significance	17	39727965	39727965	Human		name
156284813	CV1904320	single nucleotide variant	NM_004448.4(ERBB2):c.3058G>T (p.Ala1020Ser)	not provided [RCV002598517]	uncertain significance	17	39726902	39726902	Human		name
156162165	CV1906986	single nucleotide variant	NM_004448.4(ERBB2):c.3470T>G (p.Leu1157Arg)	not provided [RCV003082937]	conflicting interpretations of pathogenicity\|uncertain significance	17	39727746	39727746	Human		name
156403366	CV1908654	single nucleotide variant	NM_004448.4(ERBB2):c.3487G>A (p.Ala1163Thr)	not provided [RCV002605883]	uncertain significance	17	39727763	39727763	Human		name
155935046	CV1916337	single nucleotide variant	NM_004448.4(ERBB2):c.3541G>A (p.Val1181Ile)	not provided [RCV002615242]	uncertain significance	17	39727817	39727817	Human		name
156278608	CV1971247	single nucleotide variant	NM_004448.4(ERBB2):c.3661T>C (p.Tyr1221His)	not provided [RCV002598321]	uncertain significance	17	39727937	39727937	Human		name
156415574	CV1987321	single nucleotide variant	NM_004448.4(ERBB2):c.3523C>G (p.Pro1175Ala)	not provided [RCV002609733]	uncertain significance	17	39727799	39727799	Human		name
156142168	CV2138030	single nucleotide variant	NM_004448.4(ERBB2):c.3110C>T (p.Pro1037Leu)	Glioma susceptibility 1 [RCV005019521]\|not provided [RCV002982352]	uncertain significance	17	39726954	39726954	Human	4	name
156125341	CV2147490	single nucleotide variant	NM_004448.4(ERBB2):c.3673C>T (p.Gln1225Ter)	not provided [RCV003021962]	uncertain significance	17	39727949	39727949	Human		name
156119356	CV2183180	single nucleotide variant	NM_004448.4(ERBB2):c.3007A>G (p.Thr1003Ala)	not provided [RCV003039251]	uncertain significance	17	39726851	39726851	Human		name
156160218	CV2236322	single nucleotide variant	NM_004448.4(ERBB2):c.3675G>C (p.Gln1225His)	not specified [RCV004108016]	uncertain significance	17	39727951	39727951	Human		name
401890011	CV2763589	single nucleotide variant	NM_004448.4(ERBB2):c.3157A>G (p.Arg1053Gly)	not specified [RCV004343099]	uncertain significance	17	39727001	39727001	Human		name
405194215	CV2872415	single nucleotide variant	NM_004448.4(ERBB2):c.3215G>C (p.Arg1072Thr)	not provided [RCV003550686]	uncertain significance	17	39727350	39727350	Human		name
405112400	CV2938867	single nucleotide variant	NM_004448.4(ERBB2):c.3527G>A (p.Gly1176Glu)	not provided [RCV003666424]	uncertain significance	17	39727803	39727803	Human		name
405136350	CV3028688	single nucleotide variant	NM_004448.4(ERBB2):c.3296A>G (p.Gln1099Arg)	not provided [RCV003702135]	uncertain significance	17	39727431	39727431	Human		name
405149963	CV3031251	single nucleotide variant	NM_004448.4(ERBB2):c.3241G>T (p.Ala1081Ser)	not provided [RCV003703222]	uncertain significance	17	39727376	39727376	Human		name
405218119	CV3034821	single nucleotide variant	NM_004448.4(ERBB2):c.3514A>T (p.Thr1172Ser)	not provided [RCV003709587]	uncertain significance	17	39727790	39727790	Human		name
405084676	CV3043723	single nucleotide variant	NM_004448.4(ERBB2):c.3626C>G (p.Pro1209Arg)	not provided [RCV003717389]	uncertain significance	17	39727902	39727902	Human		name
405253881	CV3045091	single nucleotide variant	NM_004448.4(ERBB2):c.3077C>A (p.Pro1026His)	not provided [RCV003722739]	uncertain significance	17	39726921	39726921	Human		name
405246380	CV3048071	single nucleotide variant	NM_004448.4(ERBB2):c.3250G>A (p.Asp1084Asn)	not provided [RCV003720528]	uncertain significance	17	39727385	39727385	Human		name
405252162	CV3050844	single nucleotide variant	NM_004448.4(ERBB2):c.3235G>A (p.Glu1079Lys)	not provided [RCV003722097]	uncertain significance	17	39727370	39727370	Human		name
405220464	CV3059899	single nucleotide variant	NM_004448.4(ERBB2):c.3730G>A (p.Glu1244Lys)	not provided [RCV003733229]	uncertain significance	17	39728006	39728006	Human		name
405159316	CV3061723	single nucleotide variant	NM_004448.4(ERBB2):c.3086G>A (p.Gly1029Asp)	not provided [RCV003726982]	uncertain significance	17	39726930	39726930	Human		name
405120309	CV3116486	single nucleotide variant	NM_004448.4(ERBB2):c.3595C>A (p.Pro1199Thr)	not provided [RCV003814787]	uncertain significance	17	39727871	39727871	Human		name
405190249	CV3117997	single nucleotide variant	NM_004448.4(ERBB2):c.3463G>T (p.Gly1155Cys)	Glioma susceptibility 1 [RCV005015001]\|not provided [RCV003820907]	uncertain significance	17	39727739	39727739	Human	4	name
402517517	CV3135927	single nucleotide variant	NM_004448.4(ERBB2):c.3029A>G (p.Glu1010Gly)	not provided [RCV003824553]	uncertain significance	17	39726873	39726873	Human		name
405146822	CV3152059	single nucleotide variant	NM_004448.4(ERBB2):c.3493G>A (p.Ala1165Thr)	not provided [RCV003856030]	uncertain significance	17	39727769	39727769	Human		name
405247770	CV3159107	single nucleotide variant	NM_004448.4(ERBB2):c.3725C>A (p.Thr1242Lys)	not provided [RCV003869252]	uncertain significance	17	39728001	39728001	Human		name
405238141	CV3167028	single nucleotide variant	NM_004448.4(ERBB2):c.3135C>G (p.His1045Gln)	not provided [RCV003854283]	uncertain significance	17	39726979	39726979	Human		name
405248682	CV3169691	single nucleotide variant	NM_004448.4(ERBB2):c.3169G>A (p.Gly1057Arg)	not provided [RCV003869504]	uncertain significance	17	39727304	39727304	Human		name
405740914	CV3259340	single nucleotide variant	NM_004448.4(ERBB2):c.3160A>G (p.Ser1054Gly)	not specified [RCV004380478]	uncertain significance	17	39727295	39727295	Human		name
405740331	CV3259341	single nucleotide variant	NM_004448.4(ERBB2):c.3268C>G (p.Leu1090Val)	not specified [RCV004380479]	uncertain significance	17	39727403	39727403	Human		name
405740337	CV3259342	single nucleotide variant	NM_004448.4(ERBB2):c.3308C>G (p.Thr1103Arg)	not specified [RCV004380480]	uncertain significance	17	39727443	39727443	Human		name
597656203	CV3552342	single nucleotide variant	NM_004448.4(ERBB2):c.3233C>T (p.Ser1078Phe)	Lung cancer [RCV004821200]	uncertain significance	17	39727368	39727368	Human	2	name
597804158	CV3671435	single nucleotide variant	NM_004448.4(ERBB2):c.3289G>A (p.Gly1097Arg)	not specified [RCV004907554]	uncertain significance	17	39727424	39727424	Human		name
597769236	CV3709000	single nucleotide variant	NM_004448.4(ERBB2):c.3019T>A (p.Ser1007Thr)	Glioma susceptibility 1 [RCV005020214]	uncertain significance	17	39726863	39726863	Human	4	name
597889886	CV3788159	single nucleotide variant	NM_004448.4(ERBB2):c.3707C>T (p.Thr1236Ile)	not provided [RCV005125517]	uncertain significance	17	39727983	39727983	Human		name
597941750	CV3837153	single nucleotide variant	NM_004448.4(ERBB2):c.3502G>A (p.Glu1168Lys)	not provided [RCV005187984]	uncertain significance	17	39727778	39727778	Human		name
597902503	CV3851455	single nucleotide variant	NM_004448.4(ERBB2):c.3408G>T (p.Gln1136His)	not provided [RCV005202232]	uncertain significance	17	39727543	39727543	Human		name
15174786	CV727136	single nucleotide variant	NM_004448.4(ERBB2):c.3115G>A (p.Ala1039Thr)	not provided [RCV000884208]	likely benign	17	39726959	39726959	Human		name
26901757	CV845262	single nucleotide variant	NM_004448.4(ERBB2):c.3016C>T (p.Arg1006Cys)	not provided [RCV001068861]	uncertain significance	17	39726860	39726860	Human		name
26918995	CV845263	single nucleotide variant	NM_004448.4(ERBB2):c.3044G>A (p.Gly1015Glu)	Glioma susceptibility 1 [RCV005359808]\|not provided [RCV001044681]	uncertain significance	17	39726888	39726888	Human	3	name
26899592	CV845264	single nucleotide variant	NM_004448.4(ERBB2):c.3250G>T (p.Asp1084Tyr)	Visceral neuropathy, familial, 2, autosomal recessive [RCV005051855]\|not provided [RCV001067270]	uncertain significance	17	39727385	39727385	Human	1	name
26889311	CV845265	single nucleotide variant	NM_004448.4(ERBB2):c.3375T>A (p.Asp1125Glu)	not provided [RCV001058118]	uncertain significance	17	39727510	39727510	Human		name
26918904	CV845266	single nucleotide variant	NM_004448.4(ERBB2):c.3437G>A (p.Arg1146Gln)	not provided [RCV001044532]	uncertain significance	17	39727713	39727713	Human		name
26884703	CV845267	single nucleotide variant	NM_004448.4(ERBB2):c.3484C>T (p.Pro1162Ser)	not provided [RCV001052397]	uncertain significance	17	39727760	39727760	Human		name
26894977	CV845268	single nucleotide variant	NM_004448.4(ERBB2):c.3517C>G (p.Leu1173Val)	not provided [RCV001063752]	uncertain significance	17	39727793	39727793	Human		name
126755678	CV997528	single nucleotide variant	NM_004448.4(ERBB2):c.3521C>G (p.Ser1174Cys)	not provided [RCV001298407]	uncertain significance	17	39727797	39727797	Human		name
126747660	CV997529	single nucleotide variant	NM_004448.4(ERBB2):c.3763G>T (p.Val1255Leu)	not provided [RCV001306284]	uncertain significance	17	39728039	39728039	Human		name
151742390	CV1478157	deletion	NM_004448.4(ERBB2):c.383_384del (p.Pro128fs)	not provided [RCV002005936]	uncertain significance	17	39708478	39708479	Human		name
156076619	CV2011818	microsatellite	NM_004448.4(ERBB2):c.1754_1755del (p.Val585fs)	not provided [RCV002705851]	uncertain significance	17	39717331	39717332	Human		name
597967341	CV3794478	deletion	NM_004448.4(ERBB2):c.2153_2156del (p.Thr718fs)	not provided [RCV005140654]	uncertain significance	17	39723603	39723606	Human		name
597769227	CV3708999	insertion	NM_004448.4(ERBB2):c.2835_2836insT (p.Ile946fs)	Glioma susceptibility 1 [RCV005020213]	uncertain significance	17	39725816	39725817	Human	4	name
126729505	CV985878	insertion	NM_004448.4(ERBB2):c.3484_3485insG (p.Pro1162fs)	Colorectal cancer [RCV001293825]	pathogenic	17	39727760	39727761	Human	2	name
8563939	CV28916	indel	NM_004448.4(ERBB2):c.2263_2264delinsCC (p.Leu755Pro)	Lung adenocarcinoma [RCV000014891]	pathogenic\|likely pathogenic\|other	17	39723966	39723967	Human		name
8563937	CV28914	duplication	NM_004448.4(ERBB2):c.2313_2324dup (p.Tyr772_Ala775dup)	Lung adenocarcinoma [RCV000014889]\|Non-small cell lung carcinoma [RCV000038123]	pathogenic\|likely pathogenic\|other	17	39724728	39724729	Human	4	name
8563938	CV28915	duplication	NM_004448.4(ERBB2):c.2328_2336dup (p.Val777_Ser779dup)	Lung adenocarcinoma [RCV000014890]	pathogenic\|other	17	39724745	39724746	Human	2	name
12848732	CV362869	deletion	NM_004448.4(ERBB2):c.2264_2278del (p.Leu755_Thr759del)	Breast neoplasm [RCV000432652]	pathogenic	17	39723966	39723980	Human	1	name
8607822	CV54152	duplication	NM_004448.4(ERBB2):c.2314_2325dup (p.Tyr772_Ala775dup)	Lung adenocarcinoma [RCV003996361]\|Non-small cell lung carcinoma [RCV000038124]	likely pathogenic	17	39724731	39724732	Human	4	name
8607829	CV54159	duplication	NM_004448.4(ERBB2):c.2331_2339dup (p.Gly778_Pro780dup)	Lung adenocarcinoma [RCV003996362]\|Non-small cell lung carcinoma [RCV000038131]	pathogenic\|likely pathogenic	17	39724748	39724749	Human	4	name
8607830	CV54160	duplication	NM_004448.4(ERBB2):c.2332_2340dup (p.Gly778_Pro780dup)	Non-small cell lung carcinoma [RCV000038132]	likely pathogenic	17	39724749	39724750	Human	2	name
405235843	CV2887728	deletion	NM_004448.4(ERBB2):c.3674_3679del (p.Gln1225_Asp1226del)	Visceral neuropathy, familial, 2, autosomal recessive [RCV004723365]\|not provided [RCV003556380]	likely benign\|uncertain significance	17	39727945	39727950	Human	1	name
8607827	CV54157	indel	NM_004448.4(ERBB2):c.2326delinsTTAT (p.Gly776delinsLeuCys)	Non-small cell lung carcinoma [RCV000038129]	likely pathogenic	17	39724744	39724744	Human		name
8607824	CV54154	insertion	NM_004448.4(ERBB2):c.2326_2327insTCT (p.Gly776delinsValCys)	not specified [RCV000038126]	uncertain significance	17	39724744	39724745	Human		name
8607825	CV54155	insertion	NM_004448.4(ERBB2):c.2326_2327insTGT (p.Gly776delinsValCys)	Non-small cell lung carcinoma [RCV000038127]	likely pathogenic	17	39724744	39724745	Human	2	name
8607826	CV54156	insertion	NM_004448.4(ERBB2):c.2326_2327insTTT (p.Gly776delinsValCys)	Non-small cell lung carcinoma [RCV000038128]	likely pathogenic	17	39724744	39724745	Human	2	name
8607821	CV54151	duplication	ERBB2:c.2223_2234dupATACGTGATGGC (p.Gly746delinsTyrValMetAla)	Non-small cell lung cancer [RCV000038123]	likely pathogenic	17	39724731	39724742	Human	1	name
12848727	CV362872	insertion	NM_004448.4(ERBB2):c.2333_2334insGCTCCCCAG (p.Gly778_Ser779insLeuProSer)	Breast neoplasm [RCV000429589]	pathogenic	17	39724750	39724751	Human	1	name
9690696	CV176493	insertion	NM_004448.4(ERBB2):c.2324_2325insCTCCGTGATGGC (p.Ala775_Gly776insSerValMetAla)	Non-small cell lung carcinoma [RCV000156384]	likely pathogenic	17	39724733	39724734	Human	2	name
9691629	CV176631	insertion	NM_004448.4(ERBB2):c.2325_2326insTCCGTGATGGCT (p.Ala775_Gly776insSerValMetAla)	Non-small cell lung carcinoma [RCV000150653]	likely pathogenic	17	39724733	39724734	Human	2	name
8607820	CV54150	duplication	NM_001005862.2(ERBB2):c.2221_2232dupGCATACGTGATG (p.Ala745_Gly746insTyrValMetAla)	Non-small cell lung cancer [RCV000038122]	likely pathogenic	17	39724729	39724740	Human	1	name

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