ATP10A[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3131239	NM_024490.4(ATP10A):c.4475G>A (p.Gly1492Glu)	ATP10A (G1492E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3355787	NM_024490.4(ATP10A):c.4423C>A (p.Pro1475Thr)	ATP10A (P1475T)	Single nucleotide variant (missense variant)	ATP10A-related disorder	GUncertain significance
Select item 744183	NM_024490.4(ATP10A):c.4406G>A (p.Arg1469His)	ATP10A (R1469H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 741524	NM_024490.4(ATP10A):c.4406G>C (p.Arg1469Pro)	ATP10A (R1469P)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3327354	NM_024490.4(ATP10A):c.4405C>G (p.Arg1469Gly)	ATP10A (R1469G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356934	NM_024490.4(ATP10A):c.4283C>T (p.Ser1428Phe)	ATP10A (S1428F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 731567	NM_024490.4(ATP10A):c.4275C>G (p.Pro1425=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2688629	NM_024490.4(ATP10A):c.4250C>T (p.Ala1417Val)	ATP10A (A1417V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2300782	NM_024490.4(ATP10A):c.4220G>T (p.Gly1407Val)	ATP10A (G1407V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131237	NM_024490.4(ATP10A):c.4216C>A (p.Pro1406Thr)	ATP10A (P1406T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220269	NM_024490.4(ATP10A):c.4204G>C (p.Val1402Leu)	ATP10A (V1402L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3052219	NM_024490.4(ATP10A):c.4191G>A (p.Ala1397=)	ATP10A	Single nucleotide variant (synonymous variant)	ATP10A-related disorder	GLikely benign
Select item 2283640	NM_024490.4(ATP10A):c.4168G>T (p.Ala1390Ser)	ATP10A (A1390S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2404638	NM_024490.4(ATP10A):c.4123A>G (p.Met1375Val)	ATP10A (M1375V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248562	NM_024490.4(ATP10A):c.4103G>A (p.Gly1368Glu)	ATP10A (G1368E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335329	NM_024490.4(ATP10A):c.4101C>A (p.Ser1367Arg)	ATP10A (S1367R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257093	NM_024490.4(ATP10A):c.4093G>A (p.Glu1365Lys)	ATP10A (E1365K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214694	NM_024490.4(ATP10A):c.4079C>T (p.Pro1360Leu)	ATP10A (P1360L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131235	NM_024490.4(ATP10A):c.3992C>T (p.Pro1331Leu)	ATP10A (P1331L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266546	NM_024490.4(ATP10A):c.3923G>A (p.Arg1308His)	ATP10A (R1308H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264477	NM_024490.4(ATP10A):c.3910C>G (p.Leu1304Val)	ATP10A (L1304V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3059660	NM_024490.4(ATP10A):c.3894G>C (p.Arg1298Ser)	ATP10A (R1298S)	Single nucleotide variant (missense variant)	ATP10A-related disorder	GBenign
Select item 3327269	NM_024490.4(ATP10A):c.3876C>G (p.Phe1292Leu)	ATP10A (F1292L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 729418	NM_024490.4(ATP10A):c.3866+10G>A	ATP10A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 779272	NM_024490.4(ATP10A):c.3850G>A (p.Ala1284Thr)	ATP10A (A1284T)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 2645015	NM_024490.4(ATP10A):c.3801C>T (p.Ala1267=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 709275	NM_024490.4(ATP10A):c.3795G>A (p.Met1265Ile)	ATP10A (M1265I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2611305	NM_024490.4(ATP10A):c.3772C>G (p.Pro1258Ala)	ATP10A (P1258A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131234	NM_024490.4(ATP10A):c.3769C>A (p.Pro1257Thr)	ATP10A (P1257T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 722661	NM_024490.4(ATP10A):c.3750G>A (p.Ala1250=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 715937	NM_024490.4(ATP10A):c.3750G>T (p.Ala1250=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 3048371	NM_024490.4(ATP10A):c.3699G>A (p.Thr1233=)	ATP10A	Single nucleotide variant (synonymous variant)	ATP10A-related disorder	GLikely benign
Select item 3354175	NM_024490.4(ATP10A):c.3679-10T>C	ATP10A	Single nucleotide variant (intron variant)	ATP10A-related disorder	GLikely benign
Select item 3131233	NM_024490.4(ATP10A):c.3637C>T (p.Leu1213Phe)	ATP10A (L1213F)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 740085	NM_024490.4(ATP10A):c.3630C>T (p.Ile1210=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 387130	NM_024490.4(ATP10A):c.3617C>T (p.Pro1206Leu)	ATP10A (P1206L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 783702	NM_024490.4(ATP10A):c.3592G>A (p.Val1198Met)	ATP10A (V1198M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3131232	NM_024490.4(ATP10A):c.3572T>C (p.Leu1191Pro)	ATP10A (L1191P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 789330	NM_024490.4(ATP10A):c.3562A>G (p.Ile1188Val)	ATP10A (I1188V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3327288	NM_024490.4(ATP10A):c.3556T>C (p.Phe1186Leu)	ATP10A (F1186L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3060278	NM_024490.4(ATP10A):c.3516G>C (p.Trp1172Cys)	ATP10A (W1172C)	Single nucleotide variant (missense variant)	ATP10A-related disorder	GBenign
Select item 3060676	NM_024490.4(ATP10A):c.3510G>C (p.Thr1170=)	ATP10A	Single nucleotide variant (synonymous variant)	ATP10A-related disorder	GBenign
Select item 2605200	NM_024490.4(ATP10A):c.3502C>T (p.Pro1168Ser)	ATP10A (P1168S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 720963	NM_024490.4(ATP10A):c.3462G>A (p.Pro1154=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 709276	NM_024490.4(ATP10A):c.3417G>A (p.Gly1139=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2457879	NM_024490.4(ATP10A):c.3412A>T (p.Thr1138Ser)	ATP10A (T1138S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2645016	NM_024490.4(ATP10A):c.3382C>T (p.Leu1128=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2386573	NM_024490.4(ATP10A):c.3304C>T (p.Leu1102Phe)	ATP10A (L1102F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 726137	NM_024490.4(ATP10A):c.3297C>T (p.Phe1099=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2280898	NM_024490.4(ATP10A):c.3265G>A (p.Val1089Met)	ATP10A (V1089M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 747458	NM_024490.4(ATP10A):c.3243C>T (p.Cys1081=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2334802	NM_024490.4(ATP10A):c.3226C>A (p.Leu1076Ile)	ATP10A (L1076I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546947	NM_024490.4(ATP10A):c.3203G>A (p.Arg1068Gln)	ATP10A (R1068Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2232672	NM_024490.4(ATP10A):c.3194C>T (p.Pro1065Leu)	ATP10A (P1065L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2630254	NM_024490.4(ATP10A):c.3176C>T (p.Ala1059Val)	ATP10A (A1059V)	Single nucleotide variant (missense variant)	ATP10A-related disorder	GUncertain significance
Select item 3131231	NM_024490.4(ATP10A):c.3055C>T (p.Arg1019Trp)	ATP10A (R1019W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 715035	NM_024490.4(ATP10A):c.3000C>T (p.Ser1000=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 784534	NM_024490.4(ATP10A):c.2996G>A (p.Arg999His)	ATP10A (R999H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2629785	NM_024490.4(ATP10A):c.2967_2974delinsATT (p.Asp989fs)	ATP10A (D989fs)	Indel (frameshift variant)	ATP10A-related disorder	GUncertain significance
Select item 2630268	NM_024490.4(ATP10A):c.2956A>T (p.Asn986Tyr)	ATP10A (N986Y)	Single nucleotide variant (missense variant)	ATP10A-related disorder	GUncertain significance
Select item 2261376	NM_024490.4(ATP10A):c.2920A>G (p.Ile974Val)	ATP10A (I974V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 779743	NM_024490.4(ATP10A):c.2886G>A (p.Thr962=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 716405	NM_024490.4(ATP10A):c.2885C>T (p.Thr962Met)	ATP10A (T962M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3131230	NM_024490.4(ATP10A):c.2884A>T (p.Thr962Ser)	ATP10A (T962S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258733	NM_024490.4(ATP10A):c.2881T>G (p.Ser961Ala)	ATP10A (S961A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131228	NM_024490.4(ATP10A):c.2852G>T (p.Ser951Ile)	ATP10A (S951I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400095	NM_024490.4(ATP10A):c.2800G>A (p.Val934Met)	ATP10A (V934M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3048810	NM_024490.4(ATP10A):c.2790C>T (p.Cys930=)	ATP10A	Single nucleotide variant (synonymous variant)	ATP10A-related disorder	GLikely benign
Select item 2526285	NM_024490.4(ATP10A):c.2770G>T (p.Ala924Ser)	ATP10A (A924S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 756230	NM_024490.4(ATP10A):c.2766G>A (p.Ala922=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 218798	NM_024490.4(ATP10A):c.2728G>A (p.Glu910Lys)	ATP10A (E910K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 781155	NM_024490.4(ATP10A):c.2727C>T (p.Asp909=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 727596	NM_024490.4(ATP10A):c.2724C>T (p.His908=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3327363	NM_024490.4(ATP10A):c.2653A>C (p.Ile885Leu)	ATP10A (I885L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3050729	NM_024490.4(ATP10A):c.2597G>T (p.Arg866Leu)	ATP10A (R866L)	Single nucleotide variant (missense variant)	ATP10A-related disorder	GUncertain significance
Select item 3327295	NM_024490.4(ATP10A):c.2596C>T (p.Arg866Cys)	ATP10A (R866C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3037237	NM_024490.4(ATP10A):c.2550C>T (p.Arg850=)	ATP10A	Single nucleotide variant (synonymous variant)	ATP10A-related disorder	GLikely benign
Select item 1233578	NM_024490.4(ATP10A):c.2500G>A (p.Glu834Lys)	ATP10A (E834K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3061336	NM_024490.4(ATP10A):c.2444A>G (p.Lys815Arg)	ATP10A (K815R)	Single nucleotide variant (missense variant)	ATP10A-related disorder	GUncertain significance
Select item 2599280	NM_024490.4(ATP10A):c.2404G>A (p.Val802Met)	ATP10A (V802M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327344	NM_024490.4(ATP10A):c.2403C>A (p.Asn801Lys)	ATP10A (N801K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 996730	NM_024490.4(ATP10A):c.2397C>A (p.Tyr799Ter)	ATP10A (Y799*)	Single nucleotide variant (nonsense)	Autism spectrum disorder	Gassociation
Select item 2645017	NM_024490.4(ATP10A):c.2364T>C (p.His788=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1294263	NM_024490.4(ATP10A):c.2350G>A (p.Ala784Thr)	ATP10A (A784T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 736134	NM_024490.4(ATP10A):c.2328G>A (p.Leu776=)	ATP10A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2297749	NM_024490.4(ATP10A):c.2318T>C (p.Met773Thr)	ATP10A (M773T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3355037	NM_024490.4(ATP10A):c.2303C>T (p.Ala768Val)	ATP10A (A768V)	Single nucleotide variant (missense variant)	ATP10A-related disorder	GUncertain significance
Select item 2246525	NM_024490.4(ATP10A):c.2275G>A (p.Asp759Asn)	ATP10A (D759N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3327306	NM_024490.4(ATP10A):c.2269C>T (p.Leu757Phe)	ATP10A (L757F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131227	NM_024490.4(ATP10A):c.2233G>A (p.Val745Ile)	ATP10A (V745I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3131226	NM_024490.4(ATP10A):c.2205G>C (p.Glu735Asp)	ATP10A (E735D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3131225	NM_024490.4(ATP10A):c.2170G>T (p.Val724Leu)	ATP10A (V724L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2688630	NM_024490.4(ATP10A):c.2161C>G (p.Gln721Glu)	ATP10A (Q721E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3050871	NM_024490.4(ATP10A):c.2127C>T (p.Ala709=)	ATP10A	Single nucleotide variant (synonymous variant)	ATP10A-related disorder	GLikely benign
Select item 2480201	NM_024490.4(ATP10A):c.2122A>G (p.Arg708Gly)	ATP10A (R708G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131224	NM_024490.4(ATP10A):c.2068G>C (p.Glu690Gln)	ATP10A (E690Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262092	NM_024490.4(ATP10A):c.2068G>A (p.Glu690Lys)	ATP10A (E690K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131223	NM_024490.4(ATP10A):c.2058G>C (p.Glu686Asp)	ATP10A (E686D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 715051	NM_024490.4(ATP10A):c.2056G>A (p.Glu686Lys)	ATP10A (E686K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3131222	NM_024490.4(ATP10A):c.2054A>T (p.Gln685Leu)	ATP10A (Q685L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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