neptunia tolerated - ClinVar - NCBI

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The following term was not found in ClinVar: neptunia.
Showing results for Neptunia oleracea. Your search for Neptunia oleracea retrieved no results.

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 846933	NM_001385641.1(SAMD11):c.643G>A (p.Ala215Thr)	SAMD11 (A36T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1478180	NM_001385641.1(SAMD11):c.644C>T (p.Ala215Val)	SAMD11 (A36V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1380424	NM_001385641.1(SAMD11):c.650C>G (p.Pro217Arg)	SAMD11 (P217R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1354167	NM_001385641.1(SAMD11):c.650C>T (p.Pro217Leu)	SAMD11 (P38L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1043045	NM_001385641.1(SAMD11):c.655G>A (p.Ala219Thr)	SAMD11 (A219T +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2012623	NM_001385641.1(SAMD11):c.656C>T (p.Ala219Val)	SAMD11 (A219V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1715702	NM_001385641.1(SAMD11):c.683C>G (p.Pro228Arg)	SAMD11 (P228R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2122561	NM_001385641.1(SAMD11):c.685A>G (p.Ser229Gly)	SAMD11 (S229G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1499045	NM_001385641.1(SAMD11):c.715G>A (p.Gly239Arg)	SAMD11 (G239R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1473769	NM_001385641.1(SAMD11):c.716G>C (p.Gly239Ala)	SAMD11 (G239A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 969662	NM_001385641.1(SAMD11):c.730T>G (p.Cys244Gly)	SAMD11 (C65G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1505398	NM_001385641.1(SAMD11):c.767C>G (p.Pro256Arg)	SAMD11 (P77R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1359546	NM_001385641.1(SAMD11):c.775C>G (p.Arg259Gly)	SAMD11 (R259G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1478458	NM_001385641.1(SAMD11):c.776G>T (p.Arg259Leu)	SAMD11 (R259L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1379347	NM_001385641.1(SAMD11):c.874A>G (p.Ser292Gly)	SAMD11 (S113G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1897286	NM_001385641.1(SAMD11):c.877G>A (p.Val293Ile)	SAMD11 (V293I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1379812	NM_001385641.1(SAMD11):c.881A>G (p.His294Arg)	SAMD11 (H115R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2094939	NM_001385641.1(SAMD11):c.882C>A (p.His294Gln)	SAMD11 (H115Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1462622	NM_001385641.1(SAMD11):c.903G>T (p.Met301Ile)	SAMD11 (M301I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 862561	NM_001385641.1(SAMD11):c.918C>G (p.Ser306Arg)	SAMD11 (S127R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1352371	NM_001385641.1(SAMD11):c.920G>A (p.Arg307His)	SAMD11 (R128H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2013657	NM_001385641.1(SAMD11):c.927A>C (p.Glu309Asp)	SAMD11 (E130D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1365896	NM_001385641.1(SAMD11):c.959G>A (p.Arg320Gln)	SAMD11 (R141Q +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1476759	NM_001385641.1(SAMD11):c.962C>T (p.Pro321Leu)	SAMD11 (P321L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1525351	NM_001385641.1(SAMD11):c.967G>A (p.Gly323Ser)	SAMD11 (G144S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 861002	NM_001385641.1(SAMD11):c.994C>T (p.Arg332Cys)	SAMD11 (R153C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1043874	NM_001385641.1(SAMD11):c.995G>A (p.Arg332His)	SAMD11 (R153H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 857919	NM_001385641.1(SAMD11):c.1003C>T (p.Arg335Cys)	SAMD11 (R156C +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 855371	NM_001385641.1(SAMD11):c.1004G>T (p.Arg335Leu)	SAMD11 (R156L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1502284	NM_001385641.1(SAMD11):c.1045G>C (p.Glu349Gln)	SAMD11 (E170Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1427749	NM_001385641.1(SAMD11):c.1045G>A (p.Glu349Lys)	SAMD11 (E349K +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1379155	NM_001385641.1(SAMD11):c.1060G>A (p.Ala354Thr)	SAMD11 (A175T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1913584	NM_001385641.1(SAMD11):c.1080G>T (p.Glu360Asp)	SAMD11 (E181D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1346205	NM_001385641.1(SAMD11):c.1080G>C (p.Glu360Asp)	SAMD11 (E361D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1403940	NM_001385641.1(SAMD11):c.1100C>G (p.Pro367Arg)	SAMD11 (P188R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2006508	NM_001385641.1(SAMD11):c.1104G>C (p.Glu368Asp)	SAMD11 (E369D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1441376	NM_001385641.1(SAMD11):c.1120C>G (p.Leu374Val)	SAMD11 (L195V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2078010	NM_001385641.1(SAMD11):c.1127C>T (p.Ser376Leu)	SAMD11 (S197L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1514394	NM_001385641.1(SAMD11):c.1195G>A (p.Asp399Asn)	SAMD11 (D400N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1394161	NM_001385641.1(SAMD11):c.1195+46A>T	SAMD11 (H235L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2185615	NM_001385641.1(SAMD11):c.1195+48G>A	SAMD11 (D236N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1909867	NM_001385641.1(SAMD11):c.1216G>A (p.Glu406Lys)	SAMD11 (E407K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1062102	NM_001385641.1(SAMD11):c.1219G>A (p.Val407Met)	SAMD11 (V244M +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1957959	NM_001385641.1(SAMD11):c.1228G>A (p.Ala410Thr)	SAMD11 (A247T +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 935894	NM_001385641.1(SAMD11):c.1252C>G (p.Leu418Val)	SAMD11 (L255V +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1386070	NM_001385641.1(SAMD11):c.1263C>G (p.His421Gln)	SAMD11 (H422Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1951833	NM_001385641.1(SAMD11):c.1282G>A (p.Gly428Ser)	SAMD11 (G265S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1060766	NM_001385641.1(SAMD11):c.1291C>G (p.Arg431Gly)	SAMD11 (R268G +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1381806	NM_001385641.1(SAMD11):c.1312C>T (p.His438Tyr)	SAMD11 (H438Y +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2302573	NM_001385641.1(SAMD11):c.1321G>A (p.Gly441Ser)	SAMD11 (G278S +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1348363	NM_001385641.1(SAMD11):c.1322G>T (p.Gly441Val)	SAMD11 (G278V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1920718	NM_001385641.1(SAMD11):c.1327G>A (p.Ala443Thr)	SAMD11 (A280T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1006858	NM_001385641.1(SAMD11):c.1336G>A (p.Ala446Thr)	SAMD11 (A283T +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1059309	NM_001385641.1(SAMD11):c.1343C>T (p.Pro448Leu)	SAMD11 (P285L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 955893	NM_001385641.1(SAMD11):c.1350C>G (p.Phe450Leu)	SAMD11 (F287L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1056304	NM_001385641.1(SAMD11):c.1366C>T (p.Pro456Ser)	SAMD11 (P293S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 861801	NM_001385641.1(SAMD11):c.1366C>G (p.Pro456Ala)	SAMD11 (P293A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 969167	NM_001385641.1(SAMD11):c.1367C>T (p.Pro456Leu)	SAMD11 (P293L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1378409	NM_001385641.1(SAMD11):c.1369C>G (p.Gln457Glu)	SAMD11 (Q457E +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1058613	NM_001385641.1(SAMD11):c.1393C>G (p.Gln465Glu)	SAMD11 (Q302E +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2049601	NM_001385641.1(SAMD11):c.1411G>T (p.Ala471Ser)	SAMD11 (A308S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1362566	NM_001385641.1(SAMD11):c.1420C>G (p.Pro474Ala)	SAMD11 (P311A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 840316	NM_001385641.1(SAMD11):c.1420C>T (p.Pro474Ser)	SAMD11 (P311S +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1928719	NM_001385641.1(SAMD11):c.1466A>C (p.Gln489Pro)	SAMD11 (Q489P +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1046985	NM_001385641.1(SAMD11):c.1489C>T (p.Pro497Ser)	SAMD11 (P498S +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1464581	NM_001385641.1(SAMD11):c.1490C>T (p.Pro497Leu)	SAMD11 (P498L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1925806	NM_001385641.1(SAMD11):c.1567G>A (p.Ala523Thr)	SAMD11 (A523T +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1507923	NM_001385641.1(SAMD11):c.1598G>A (p.Ser533Asn)	SAMD11 (S533N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 860480	NM_001385641.1(SAMD11):c.1609C>A (p.Gln537Lys)	SAMD11 (Q374K +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1903672	NM_001385641.1(SAMD11):c.1621C>G (p.Pro541Ala)	SAMD11 (P378A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1370052	NM_001385641.1(SAMD11):c.1628C>G (p.Thr543Ser)	SAMD11 (T544S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1044532	NM_001385641.1(SAMD11):c.1637G>A (p.Arg546His)	SAMD11 (R383H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2092501	NM_001385641.1(SAMD11):c.1642A>G (p.Asn548Asp)	SAMD11 (N549D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 965463	NM_001385641.1(SAMD11):c.1643A>G (p.Asn548Ser)	SAMD11 (N385S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1502527	NM_001385641.1(SAMD11):c.1644C>G (p.Asn548Lys)	SAMD11 (N385K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1473596	NM_001385641.1(SAMD11):c.1720C>T (p.Pro574Ser)	SAMD11 (P574S +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1946658	NM_001385641.1(SAMD11):c.1738G>C (p.Gly580Arg)	SAMD11 (G417R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2088345	NM_001385641.1(SAMD11):c.1747C>T (p.Pro583Ser)	SAMD11 (P420S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 999421	NM_001385641.1(SAMD11):c.1747C>A (p.Pro583Thr)	SAMD11 (P420T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1523574	NM_001385641.1(SAMD11):c.1768T>A (p.Ser590Thr)	SAMD11 (S427T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 838673	NM_001385641.1(SAMD11):c.1771G>A (p.Ala591Thr)	SAMD11 (A428T +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2017041	NM_001385641.1(SAMD11):c.1790A>G (p.Lys597Arg)	SAMD11 (K597R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 840797	NM_001385641.1(SAMD11):c.1795G>A (p.Gly599Ser)	SAMD11 (G436S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1908032	NM_001385641.1(SAMD11):c.1807G>C (p.Ala603Pro)	SAMD11 (A604P +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1935101	NM_001385641.1(SAMD11):c.1810T>A (p.Ser604Thr)	SAMD11 (S605T +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1496990	NM_001385641.1(SAMD11):c.1813G>T (p.Ala605Ser)	SAMD11 (A605S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1042884	NM_001385641.1(SAMD11):c.1814C>T (p.Ala605Val)	SAMD11 (A442V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2421646	NM_001385641.1(SAMD11):c.1817G>A (p.Arg606Gln)	SAMD11 (R443Q +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1378233	NM_001385641.1(SAMD11):c.1820C>G (p.Pro607Arg)	SAMD11 (P444R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1060504	NM_001385641.1(SAMD11):c.1829C>T (p.Ser610Phe)	SAMD11 (S447F +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1978445	NM_001385641.1(SAMD11):c.1841C>A (p.Thr614Lys)	SAMD11 (T615K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 943743	NM_001385641.1(SAMD11):c.1846G>A (p.Ala616Thr)	SAMD11 (A453T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1714234	NM_001385641.1(SAMD11):c.1849A>G (p.Arg617Gly)	SAMD11 (R454G +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1507134	NM_001385641.1(SAMD11):c.1855T>C (p.Trp619Arg)	SAMD11 (W456R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 972129	NM_001385641.1(SAMD11):c.1859C>T (p.Ala620Val)	SAMD11 (A457V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1424531	NM_001385641.1(SAMD11):c.1867G>A (p.Gly623Ser)	SAMD11 (G623S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1965813	NM_001385641.1(SAMD11):c.1868G>A (p.Gly623Asp)	SAMD11 (G460D +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2001120	NM_001385641.1(SAMD11):c.1870T>C (p.Ser624Pro)	SAMD11 (S624P +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 969727	NM_001385641.1(SAMD11):c.1882C>T (p.Pro628Ser)	SAMD11 (P465S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1056825	NM_001385641.1(SAMD11):c.1886C>G (p.Pro629Arg)	SAMD11 (P466R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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