ANKRD12[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2632650	NM_015208.5(ANKRD12):c.64G>T (p.Val22Leu)	ANKRD12 (V22L)	Single nucleotide variant (missense variant)	ANKRD12-related disorder	GUncertain significance
Select item 2339707	NM_015208.5(ANKRD12):c.86A>C (p.Lys29Thr)	ANKRD12 (K29T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474700	NM_015208.5(ANKRD12):c.92A>G (p.Lys31Arg)	ANKRD12 (K31R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399737	NM_015208.5(ANKRD12):c.154A>G (p.Met52Val)	ANKRD12 (M52V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486911	NM_015208.5(ANKRD12):c.250C>T (p.His84Tyr)	ANKRD12 (H84Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2388100	NM_015208.5(ANKRD12):c.264T>G (p.Asn88Lys)	ANKRD12 (N88K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122763	NM_015208.5(ANKRD12):c.319G>C (p.Glu107Gln)	ANKRD12 (E84Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257131	NM_015208.5(ANKRD12):c.336A>C (p.Lys112Asn)	ANKRD12 (K112N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375691	NM_015208.5(ANKRD12):c.370A>G (p.Ser124Gly)	ANKRD12 (S124G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122886	NM_015208.5(ANKRD12):c.521A>C (p.Gln174Pro)	ANKRD12 (Q151P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122902	NM_015208.5(ANKRD12):c.542G>T (p.Arg181Ile)	ANKRD12 (R158I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2636230	NM_015208.5(ANKRD12):c.877A>G (p.Thr293Ala)	ANKRD12 (T270A +1 more)	Single nucleotide variant (missense variant)	ANKRD12-related disorder	GUncertain significance
Select item 2360812	NM_015208.5(ANKRD12):c.971C>T (p.Pro324Leu)	ANKRD12 (P324L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337372	NM_015208.5(ANKRD12):c.1246C>A (p.Gln416Lys)	ANKRD12 (Q393K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296346	NM_015208.5(ANKRD12):c.1321A>G (p.Thr441Ala)	ANKRD12 (T441A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3296335	NM_015208.5(ANKRD12):c.1333G>A (p.Val445Ile)	ANKRD12 (V422I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483910	NM_015208.5(ANKRD12):c.1379A>G (p.Tyr460Cys)	ANKRD12 (Y460C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554226	NM_015208.5(ANKRD12):c.1559A>G (p.Asn520Ser)	ANKRD12 (N520S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284763	NM_015208.5(ANKRD12):c.1565G>A (p.Arg522Lys)	ANKRD12 (R522K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338068	NM_015208.5(ANKRD12):c.1570T>A (p.Ser524Thr)	ANKRD12 (S524T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363264	NM_015208.5(ANKRD12):c.1571C>G (p.Ser524Cys)	ANKRD12 (S501C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360862	NM_015208.5(ANKRD12):c.1610A>G (p.His537Arg)	ANKRD12 (H537R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557078	NM_015208.5(ANKRD12):c.1619C>T (p.Thr540Ile)	ANKRD12 (T540I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489939	NM_015208.5(ANKRD12):c.1736A>T (p.Asp579Val)	ANKRD12 (D579V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320657	NM_015208.5(ANKRD12):c.1738C>A (p.Leu580Ile)	ANKRD12 (L557I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296351	NM_015208.5(ANKRD12):c.1751A>G (p.Asp584Gly)	ANKRD12 (D561G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314485	NM_015208.5(ANKRD12):c.1757C>G (p.Thr586Arg)	ANKRD12 (T563R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2648564	NM_015208.5(ANKRD12):c.1816A>G (p.Ser606Gly)	ANKRD12 (S583G +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3122703	NM_015208.5(ANKRD12):c.1817G>A (p.Ser606Asn)	ANKRD12 (S606N +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2270960	NM_015208.5(ANKRD12):c.1823A>T (p.His608Leu)	ANKRD12 (H608L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122711	NM_015208.5(ANKRD12):c.1898T>G (p.Phe633Cys)	ANKRD12 (F610C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371012	NM_015208.5(ANKRD12):c.2018A>C (p.Lys673Thr)	ANKRD12 (K650T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2203880	NM_015208.5(ANKRD12):c.2036A>G (p.Lys679Arg)	ANKRD12 (K679R +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2281442	NM_015208.5(ANKRD12):c.2048A>G (p.Lys683Arg)	ANKRD12 (K660R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477491	NM_015208.5(ANKRD12):c.2050G>C (p.Glu684Gln)	ANKRD12 (E661Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2630518	NM_015208.5(ANKRD12):c.2186del (p.Asn729fs)	ANKRD12 (N706fs +1 more)	Deletion (frameshift variant)	ANKRD12-related disorder	GUncertain significance
Select item 2377587	NM_015208.5(ANKRD12):c.2186A>C (p.Asn729Thr)	ANKRD12 (N706T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515173	NM_015208.5(ANKRD12):c.2234G>A (p.Arg745Lys)	ANKRD12 (R722K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603349	NM_015208.5(ANKRD12):c.2329A>G (p.Ile777Val)	ANKRD12 (I754V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2266432	NM_015208.5(ANKRD12):c.2363T>G (p.Leu788Trp)	ANKRD12 (L788W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296339	NM_015208.5(ANKRD12):c.2442T>G (p.His814Gln)	ANKRD12 (H814Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 219339	NM_015208.5(ANKRD12):c.2593G>T (p.Asp865Tyr)	ANKRD12 (D842Y +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 931765	NM_015208.5(ANKRD12):c.2600_2604del (p.Ile867fs)	ANKRD12 (I844fs +1 more)	Microsatellite (frameshift variant)	See cases	GUncertain significance
Select item 2370289	NM_015208.5(ANKRD12):c.2663G>A (p.Ser888Asn)	ANKRD12 (S865N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296342	NM_015208.5(ANKRD12):c.2690C>A (p.Thr897Asn)	ANKRD12 (T897N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306777	NM_015208.5(ANKRD12):c.2698A>G (p.Arg900Gly)	ANKRD12 (R900G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380827	NM_015208.5(ANKRD12):c.2746C>T (p.Pro916Ser)	ANKRD12 (P916S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305781	NM_015208.5(ANKRD12):c.2797A>G (p.Lys933Glu)	ANKRD12 (K910E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296352	NM_015208.5(ANKRD12):c.2806A>G (p.Lys936Glu)	ANKRD12 (K936E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210350	NM_015208.5(ANKRD12):c.2819A>G (p.Asn940Ser)	ANKRD12 (N917S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2629600	NM_015208.5(ANKRD12):c.2897A>C (p.Asp966Ala)	ANKRD12 (D943A +1 more)	Single nucleotide variant (missense variant)	ANKRD12-related disorder	GUncertain significance
Select item 3040962	NM_015208.5(ANKRD12):c.2924C>A (p.Ser975Tyr)	ANKRD12 (S952Y +1 more)	Single nucleotide variant (missense variant)	ANKRD12-related disorder	GLikely benign
Select item 2392314	NM_015208.5(ANKRD12):c.2951C>T (p.Ser984Leu)	ANKRD12 (S984L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375584	NM_015208.5(ANKRD12):c.3034C>A (p.Pro1012Thr)	ANKRD12 (P1012T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459622	NM_015208.5(ANKRD12):c.3140C>A (p.Ser1047Tyr)	ANKRD12 (S1024Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336618	NM_015208.5(ANKRD12):c.3145G>A (p.Ala1049Thr)	ANKRD12 (A1049T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322613	NM_015208.5(ANKRD12):c.3236G>A (p.Ser1079Asn)	ANKRD12 (S1056N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2624310	NM_015208.5(ANKRD12):c.3292C>T (p.His1098Tyr)	ANKRD12 (H1075Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459623	NM_015208.5(ANKRD12):c.3352C>T (p.Leu1118Phe)	ANKRD12 (L1095F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296337	NM_015208.5(ANKRD12):c.3353T>G (p.Leu1118Arg)	ANKRD12 (L1118R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296350	NM_015208.5(ANKRD12):c.3382C>T (p.His1128Tyr)	ANKRD12 (H1105Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122779	NM_015208.5(ANKRD12):c.3437T>C (p.Val1146Ala)	ANKRD12 (V1123A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326803	NM_015208.5(ANKRD12):c.3491C>T (p.Ser1164Leu)	ANKRD12 (S1141L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296333	NM_015208.5(ANKRD12):c.3497C>G (p.Ser1166Cys)	ANKRD12 (S1143C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122780	NM_015208.5(ANKRD12):c.3521C>T (p.Thr1174Ile)	ANKRD12 (T1174I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211315	NM_015208.5(ANKRD12):c.3524T>C (p.Leu1175Ser)	ANKRD12 (L1175S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535804	NM_015208.5(ANKRD12):c.3532T>G (p.Ser1178Ala)	ANKRD12 (S1178A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343017	NM_015208.5(ANKRD12):c.3919G>A (p.Val1307Ile)	ANKRD12 (V1284I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260212	NM_015208.5(ANKRD12):c.3958A>G (p.Thr1320Ala)	ANKRD12 (T1320A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508129	NM_015208.5(ANKRD12):c.3967T>C (p.Phe1323Leu)	ANKRD12 (F1300L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122796	NM_015208.5(ANKRD12):c.4012G>C (p.Val1338Leu)	ANKRD12 (V1315L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221594	NM_015208.5(ANKRD12):c.4081A>G (p.Asn1361Asp)	ANKRD12 (N1361D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362973	NM_015208.5(ANKRD12):c.4084G>T (p.Val1362Leu)	ANKRD12 (V1362L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122806	NM_015208.5(ANKRD12):c.4093A>G (p.Ile1365Val)	ANKRD12 (I1342V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296340	NM_015208.5(ANKRD12):c.4100C>G (p.Ser1367Cys)	ANKRD12 (S1367C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122810	NM_015208.5(ANKRD12):c.4165A>G (p.Ile1389Val)	ANKRD12 (I1366V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375380	NM_015208.5(ANKRD12):c.4187A>G (p.Asn1396Ser)	ANKRD12 (N1373S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2536133	NM_015208.5(ANKRD12):c.4217A>C (p.Glu1406Ala)	ANKRD12 (E1383A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532276	NM_015208.5(ANKRD12):c.4228C>G (p.Gln1410Glu)	ANKRD12 (Q1387E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283832	NM_015208.5(ANKRD12):c.4292C>G (p.Thr1431Ser)	ANKRD12 (T1408S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3047967	NM_015208.5(ANKRD12):c.4312A>G (p.Asn1438Asp)	ANKRD12 (N1415D +1 more)	Single nucleotide variant (missense variant)	ANKRD12-related disorder	GLikely benign
Select item 2310670	NM_015208.5(ANKRD12):c.4348A>G (p.Ser1450Gly)	ANKRD12 (S1427G +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3296338	NM_015208.5(ANKRD12):c.4363G>A (p.Glu1455Lys)	ANKRD12 (E1455K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330905	NM_015208.5(ANKRD12):c.4436C>T (p.Ala1479Val)	ANKRD12 (A1456V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122828	NM_015208.5(ANKRD12):c.4459C>T (p.Pro1487Ser)	ANKRD12 (P1487S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122834	NM_015208.5(ANKRD12):c.4527G>A (p.Met1509Ile)	ANKRD12 (M1486I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122837	NM_015208.5(ANKRD12):c.4537T>C (p.Tyr1513His)	ANKRD12 (Y1490H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339977	NM_015208.5(ANKRD12):c.4548T>A (p.Asn1516Lys)	ANKRD12 (N1516K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525693	NM_015208.5(ANKRD12):c.4660G>A (p.Val1554Ile)	ANKRD12 (V1531I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404967	NM_015208.5(ANKRD12):c.4669A>C (p.Thr1557Pro)	ANKRD12 (T1557P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229270	NM_015208.5(ANKRD12):c.4698C>G (p.Asp1566Glu)	ANKRD12 (D1543E +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3122852	NM_015208.5(ANKRD12):c.4717T>C (p.Ser1573Pro)	ANKRD12 (S1550P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395130	NM_015208.5(ANKRD12):c.4823A>G (p.Lys1608Arg)	ANKRD12 (K1585R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340708	NM_015208.5(ANKRD12):c.4831T>G (p.Tyr1611Asp)	ANKRD12 (Y1611D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309184	NM_015208.5(ANKRD12):c.4836G>C (p.Lys1612Asn)	ANKRD12 (K1612N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345571	NM_015208.5(ANKRD12):c.4943G>A (p.Cys1648Tyr)	ANKRD12 (C1648Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296343	NM_015208.5(ANKRD12):c.4958G>A (p.Cys1653Tyr)	ANKRD12 (C1630Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122870	NM_015208.5(ANKRD12):c.5035T>A (p.Leu1679Met)	ANKRD12 (L1656M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361179	NM_015208.5(ANKRD12):c.5044A>G (p.Ile1682Val)	ANKRD12 (I1682V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3033713	NM_015208.5(ANKRD12):c.5078C>G (p.Ser1693Ter)	ANKRD12 (S1670* +1 more)	Single nucleotide variant (nonsense)	ANKRD12-related disorder	GUncertain significance

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