"Ambry Genetics"[submitter] AND "ATP10D"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 82

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2274250	NM_020453.4(ATP10D):c.77G>A (p.Gly26Glu)	ATP10D (G26E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131288	NM_020453.4(ATP10D):c.80C>G (p.Pro27Arg)	ATP10D (P27R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410908	NM_020453.4(ATP10D):c.89A>G (p.Tyr30Cys)	ATP10D (Y30C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369356	NM_020453.4(ATP10D):c.95C>T (p.Ser32Leu)	ATP10D (S32L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269885	NM_020453.4(ATP10D):c.285T>A (p.Phe95Leu)	ATP10D (F95L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283738	NM_020453.4(ATP10D):c.329A>G (p.Asn110Ser)	ATP10D (N110S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131284	NM_020453.4(ATP10D):c.410A>C (p.Lys137Thr)	ATP10D (K137T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131287	NM_020453.4(ATP10D):c.431G>A (p.Arg144Gln)	ATP10D (R144Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611484	NM_020453.4(ATP10D):c.439A>G (p.Lys147Glu)	ATP10D (K147E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269690	NM_020453.4(ATP10D):c.479A>G (p.Tyr160Cys)	ATP10D (Y160C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403538	NM_020453.4(ATP10D):c.559G>A (p.Glu187Lys)	ATP10D (E187K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272139	NM_020453.4(ATP10D):c.660G>C (p.Gln220His)	ATP10D (Q220H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327575	NM_020453.4(ATP10D):c.721A>G (p.Ser241Gly)	ATP10D (S241G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470269	NM_020453.4(ATP10D):c.767G>A (p.Arg256Gln)	ATP10D (R256Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214054	NM_020453.4(ATP10D):c.797G>A (p.Arg266His)	ATP10D (R266H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359674	NM_020453.4(ATP10D):c.799G>A (p.Val267Met)	ATP10D (V267M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327528	NM_020453.4(ATP10D):c.886C>T (p.His296Tyr)	ATP10D (H296Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398710	NM_020453.4(ATP10D):c.932G>A (p.Arg311His)	ATP10D (R311H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327594	NM_020453.4(ATP10D):c.979A>G (p.Met327Val)	ATP10D (M327V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547287	NM_020453.4(ATP10D):c.1028G>T (p.Trp343Leu)	ATP10D (W343L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615083	NM_020453.4(ATP10D):c.1035C>A (p.Ser345Arg)	ATP10D (S345R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371681	NM_020453.4(ATP10D):c.1046A>G (p.Lys349Arg)	ATP10D (K349R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327542	NM_020453.4(ATP10D):c.1166A>C (p.Tyr389Ser)	ATP10D (Y389S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228934	NM_020453.4(ATP10D):c.1201T>C (p.Tyr401His)	ATP10D (Y401H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131274	NM_020453.4(ATP10D):c.1207A>G (p.Ile403Val)	ATP10D (I403V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509620	NM_020453.4(ATP10D):c.1237A>G (p.Lys413Glu)	ATP10D (K413E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559541	NM_020453.4(ATP10D):c.1257G>T (p.Gln419His)	ATP10D (Q419H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327535	NM_020453.4(ATP10D):c.1312G>A (p.Asp438Asn)	ATP10D (D438N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368580	NM_020453.4(ATP10D):c.1436A>T (p.Asp479Val)	ATP10D (D479V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333327	NM_020453.4(ATP10D):c.1441G>A (p.Asp481Asn)	ATP10D (D481N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285423	NM_020453.4(ATP10D):c.1487C>T (p.Pro496Leu)	ATP10D (P496L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278549	NM_020453.4(ATP10D):c.1498A>G (p.Ser500Gly)	ATP10D (S500G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469507	NM_020453.4(ATP10D):c.1502G>A (p.Cys501Tyr)	ATP10D (C501Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131276	NM_020453.4(ATP10D):c.1634T>C (p.Ile545Thr)	ATP10D (I545T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217969	NM_020453.4(ATP10D):c.1670A>G (p.Asp557Gly)	ATP10D (D557G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375266	NM_020453.4(ATP10D):c.1693C>T (p.Arg565Trp)	ATP10D (R565W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510495	NM_020453.4(ATP10D):c.1817G>A (p.Arg606Gln)	ATP10D (R606Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254129	NM_020453.4(ATP10D):c.1847G>A (p.Gly616Glu)	ATP10D (G616E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204145	NM_020453.4(ATP10D):c.1904G>A (p.Arg635Gln)	ATP10D (R635Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386955	NM_020453.4(ATP10D):c.1922C>T (p.Ser641Leu)	ATP10D (S641L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327602	NM_020453.4(ATP10D):c.1994G>C (p.Arg665Pro)	ATP10D (R665P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521236	NM_020453.4(ATP10D):c.2039G>A (p.Cys680Tyr)	ATP10D (C680Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407332	NM_020453.4(ATP10D):c.2048C>T (p.Pro683Leu)	ATP10D (P683L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312493	NM_020453.4(ATP10D):c.2104G>A (p.Ala702Thr)	ATP10D (A702T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522583	NM_020453.4(ATP10D):c.2108G>C (p.Gly703Ala)	ATP10D (G703A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131278	NM_020453.4(ATP10D):c.2125G>A (p.Ala709Thr)	ATP10D (A709T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607881	NM_020453.4(ATP10D):c.2176G>A (p.Glu726Lys)	ATP10D (E726K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323967	NM_020453.4(ATP10D):c.2239C>T (p.Arg747Trp)	ATP10D (R747W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396528	NM_020453.4(ATP10D):c.2269G>C (p.Ala757Pro)	ATP10D (A757P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215925	NM_020453.4(ATP10D):c.2279G>A (p.Gly760Glu)	ATP10D (G760E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607882	NM_020453.4(ATP10D):c.2287A>G (p.Thr763Ala)	ATP10D (T763A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131279	NM_020453.4(ATP10D):c.2640G>A (p.Met880Ile)	ATP10D (M880I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276235	NM_020453.4(ATP10D):c.2717T>C (p.Ile906Thr)	ATP10D (I906T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211486	NM_020453.4(ATP10D):c.2728C>A (p.His910Asn)	ATP10D (H910N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465308	NM_020453.4(ATP10D):c.2740A>G (p.Ile914Val)	ATP10D (I914V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369579	NM_020453.4(ATP10D):c.2782G>A (p.Val928Ile)	ATP10D (V928I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211663	NM_020453.4(ATP10D):c.2881A>G (p.Ile961Val)	ATP10D (I961V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476994	NM_020453.4(ATP10D):c.2965C>G (p.Arg989Gly)	ATP10D (R989G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486020	NM_020453.4(ATP10D):c.3044A>G (p.Gln1015Arg)	ATP10D (Q1015R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131280	NM_020453.4(ATP10D):c.3089G>A (p.Arg1030Gln)	ATP10D (R1030Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337672	NM_020453.4(ATP10D):c.3233G>T (p.Gly1078Val)	ATP10D (G1078V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408805	NM_020453.4(ATP10D):c.3237G>T (p.Met1079Ile)	ATP10D (M1079I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468488	NM_020453.4(ATP10D):c.3265G>A (p.Val1089Ile)	ATP10D (V1089I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3131281	NM_020453.4(ATP10D):c.3399C>G (p.Phe1133Leu)	ATP10D (F1133L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213409	NM_020453.4(ATP10D):c.3505G>A (p.Asp1169Asn)	ATP10D (D1169N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391411	NM_020453.4(ATP10D):c.3614A>G (p.Tyr1205Cys)	ATP10D (Y1205C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327582	NM_020453.4(ATP10D):c.3668C>T (p.Thr1223Ile)	ATP10D (T1223I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2212330	NM_020453.4(ATP10D):c.3698A>T (p.Asn1233Ile)	ATP10D (N1233I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327553	NM_020453.4(ATP10D):c.3706G>A (p.Ala1236Thr)	ATP10D (A1236T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392137	NM_020453.4(ATP10D):c.3779T>C (p.Ile1260Thr)	ATP10D (I1260T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3327613	NM_020453.4(ATP10D):c.3840C>G (p.Cys1280Trp)	ATP10D (C1280W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131282	NM_020453.4(ATP10D):c.3880A>G (p.Met1294Val)	ATP10D (M1294V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474782	NM_020453.4(ATP10D):c.3898T>A (p.Tyr1300Asn)	ATP10D (Y1300N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257442	NM_020453.4(ATP10D):c.3904G>A (p.Val1302Ile)	ATP10D (V1302I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3131283	NM_020453.4(ATP10D):c.3917C>T (p.Thr1306Met)	ATP10D (T1306M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277865	NM_020453.4(ATP10D):c.3965G>A (p.Gly1322Glu)	ATP10D (G1322E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327564	NM_020453.4(ATP10D):c.4088A>G (p.Tyr1363Cys)	ATP10D (Y1363C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282819	NM_020453.4(ATP10D):c.4145T>C (p.Val1382Ala)	ATP10D (V1382A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257249	NM_020453.4(ATP10D):c.4177A>G (p.Ile1393Val)	ATP10D (I1393V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2569723	NM_020453.4(ATP10D):c.4180G>C (p.Glu1394Gln)	ATP10D (E1394Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371373	NM_020453.4(ATP10D):c.4195T>C (p.Ser1399Pro)	ATP10D (S1399P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3131285	NM_020453.4(ATP10D):c.4268G>A (p.Gly1423Asp)	ATP10D (G1423D)	Single nucleotide variant (missense variant)	not specified	GLikely benign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 82