MCM3AP[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1226905	NM_003906.5(MCM3AP):c.4137-94T>C	MCM3AP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290157	NM_003906.5(MCM3AP):c.4137-113C>T	MCM3AP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2055866	NM_003906.5(MCM3AP):c.4101G>A (p.Pro1367=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1985050	NM_003906.5(MCM3AP):c.4100C>T (p.Pro1367Leu)	MCM3AP (P1367L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1353413	NM_003906.5(MCM3AP):c.4100C>G (p.Pro1367Arg)	MCM3AP (P1367R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2046048	NM_003906.5(MCM3AP):c.4089G>A (p.Val1363=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1896819	NM_003906.5(MCM3AP):c.4087G>T (p.Val1363Leu)	MCM3AP (V1363L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1502685	NM_003906.5(MCM3AP):c.4078T>G (p.Trp1360Gly)	MCM3AP (W1360G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1433251	NM_003906.5(MCM3AP):c.4064A>G (p.Gln1355Arg)	MCM3AP (Q1355R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1374947	NM_003906.5(MCM3AP):c.4058G>A (p.Gly1353Glu)	MCM3AP (G1353E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2608431	NM_003906.5(MCM3AP):c.4045G>C (p.Glu1349Gln)	MCM3AP (E1349Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1421611	NM_003906.5(MCM3AP):c.4039G>A (p.Val1347Met)	MCM3AP (V1347M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1899345	NM_003906.5(MCM3AP):c.4038C>T (p.Leu1346=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1497760	NM_003906.5(MCM3AP):c.4033T>C (p.Ser1345Pro)	MCM3AP (S1345P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1298885	NM_003906.5(MCM3AP):c.4017G>A (p.Ala1339=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1926015	NM_003906.5(MCM3AP):c.4016C>T (p.Ala1339Val)	MCM3AP (A1339V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2113674	NM_003906.5(MCM3AP):c.4015del (p.Ala1339fs)	MCM3AP (A1339fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 1467120	NM_003906.5(MCM3AP):c.4009G>A (p.Ala1337Thr)	MCM3AP (A1337T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1521368	NM_003906.5(MCM3AP):c.4006G>A (p.Val1336Met)	MCM3AP (V1336M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1619520	NM_003906.5(MCM3AP):c.4002-3C>T	MCM3AP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1591035	NM_003906.5(MCM3AP):c.4002-6_4002-3del	MCM3AP	Deletion (intron variant)	not provided	GLikely benign
Select item 2012415	NM_003906.5(MCM3AP):c.4002-6T>C	MCM3AP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2090128	NM_003906.5(MCM3AP):c.4002-7C>G	MCM3AP	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1529180	NM_003906.5(MCM3AP):c.4002-11G>A	MCM3AP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867693	NM_003906.5(MCM3AP):c.4002-15G>A	MCM3AP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1466709	NM_003906.5(MCM3AP):c.4002-19G>A	MCM3AP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1273420	NM_003906.5(MCM3AP):c.4002-20C>T	MCM3AP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2962092	NM_003906.5(MCM3AP):c.4001+17C>T	MCM3AP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1981720	NM_003906.5(MCM3AP):c.4001+7C>G	MCM3AP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2193988	NM_003906.5(MCM3AP):c.3998T>C (p.Leu1333Pro)	MCM3AP (L1333P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2299614	NM_003906.5(MCM3AP):c.3992A>G (p.Gln1331Arg)	MCM3AP (Q1331R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2067031	NM_003906.5(MCM3AP):c.3986A>G (p.Tyr1329Cys)	MCM3AP (Y1329C)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1912411	NM_003906.5(MCM3AP):c.3981C>T (p.His1327=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2011109	NM_003906.5(MCM3AP):c.3969G>T (p.Met1323Ile)	MCM3AP (M1323I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1487543	NM_003906.5(MCM3AP):c.3963C>G (p.His1321Gln)	MCM3AP (H1321Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1511944	NM_003906.5(MCM3AP):c.3955A>G (p.Thr1319Ala)	MCM3AP (T1319A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2576048	NM_003906.5(MCM3AP):c.3949_3950insG (p.Asn1317fs)	MCM3AP (N1317fs)	Insertion (frameshift variant)	not provided	GLikely pathogenic
Select item 1399489	NM_003906.5(MCM3AP):c.3941G>A (p.Arg1314Gln)	MCM3AP (R1314Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 725171	NM_003906.5(MCM3AP):c.3940C>T (p.Arg1314Trp)	MCM3AP (R1314W)	Single nucleotide variant (missense variant)	MCM3AP-related disorder +1 more	GLikely benign
Select item 2113664	NM_003906.5(MCM3AP):c.3935T>G (p.Leu1312Ter)	MCM3AP (L1312*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2970703	NM_003906.5(MCM3AP):c.3933-1G>T	MCM3AP	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 1912725	NM_003906.5(MCM3AP):c.3933-13C>G	MCM3AP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1566608	NM_003906.5(MCM3AP):c.3933-20C>T	MCM3AP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1947276	NM_003906.5(MCM3AP):c.3932+19C>G	MCM3AP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1948607	NM_003906.5(MCM3AP):c.3932+17G>A	MCM3AP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1960426	NM_003906.5(MCM3AP):c.3932+16C>T	MCM3AP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1966144	NM_003906.5(MCM3AP):c.3932+11G>A	MCM3AP	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1928367	NM_003906.5(MCM3AP):c.3929C>G (p.Thr1310Ser)	MCM3AP (T1310S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1244926	NM_003906.5(MCM3AP):c.3924C>T (p.Ser1308=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2827888	NM_003906.5(MCM3AP):c.3918C>T (p.Gly1306=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1974932	NM_003906.5(MCM3AP):c.3904G>A (p.Ala1302Thr)	MCM3AP (A1302T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2862947	NM_003906.5(MCM3AP):c.3900C>G (p.Gly1300=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3124337	NM_003906.5(MCM3AP):c.3899G>A (p.Gly1300Asp)	MCM3AP (G1300D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3124336	NM_003906.5(MCM3AP):c.3898G>A (p.Gly1300Ser)	MCM3AP (G1300S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1381337	NM_003906.5(MCM3AP):c.3895C>G (p.Leu1299Val)	MCM3AP (L1299V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1571758	NM_003906.5(MCM3AP):c.3889C>T (p.Leu1297=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1471473	NM_003906.5(MCM3AP):c.3882G>T (p.Arg1294Ser)	MCM3AP (R1294S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1522199	NM_003906.5(MCM3AP):c.3869A>G (p.Glu1290Gly)	MCM3AP (E1290G)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1995928	NM_003906.5(MCM3AP):c.3864T>C (p.Ala1288=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1510393	NM_003906.5(MCM3AP):c.3860T>C (p.Ile1287Thr)	MCM3AP (I1287T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1699601	NM_003906.5(MCM3AP):c.3859A>G (p.Ile1287Val)	MCM3AP (I1287V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1715094	NM_003906.5(MCM3AP):c.3857C>A (p.Pro1286His)	MCM3AP (P1286H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1629895	NM_003906.5(MCM3AP):c.3855C>T (p.Cys1285=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1547717	NM_003906.5(MCM3AP):c.3849A>G (p.Ala1283=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1363806	NM_003906.5(MCM3AP):c.3847G>A (p.Ala1283Thr)	MCM3AP (A1283T)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1413181	NM_003906.5(MCM3AP):c.3839C>T (p.Ala1280Val)	MCM3AP (A1280V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1535821	NM_003906.5(MCM3AP):c.3834G>A (p.Ala1278=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2075196	NM_003906.5(MCM3AP):c.3833C>G (p.Ala1278Gly)	MCM3AP (A1278G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1517840	NM_003906.5(MCM3AP):c.3833C>T (p.Ala1278Val)	MCM3AP (A1278V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1579833	NM_003906.5(MCM3AP):c.3826C>T (p.Leu1276=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1450067	NM_003906.5(MCM3AP):c.3824G>A (p.Arg1275Gln)	MCM3AP (R1275Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1403223	NM_003906.5(MCM3AP):c.3824G>T (p.Arg1275Leu)	MCM3AP (R1275L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1924414	NM_003906.5(MCM3AP):c.3823C>T (p.Arg1275Trp)	MCM3AP (R1275W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1405249	NM_003906.5(MCM3AP):c.3820G>A (p.Asp1274Asn)	MCM3AP (D1274N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1919710	NM_003906.5(MCM3AP):c.3819C>T (p.Ser1273=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 562048	NM_003906.5(MCM3AP):c.3814G>A (p.Val1272Met)	MCM3AP (V1272M)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1609551	NM_003906.5(MCM3AP):c.3813C>T (p.Asp1271=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1716089	NM_003906.5(MCM3AP):c.3811G>C (p.Asp1271His)	MCM3AP (D1271H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1957831	NM_003906.5(MCM3AP):c.3809T>C (p.Val1270Ala)	MCM3AP (V1270A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 817943	NM_003906.5(MCM3AP):c.3799_3808dup (p.Val1270fs)	MCM3AP (V1270fs)	Microsatellite (frameshift variant)	not provided	GPathogenic
Select item 1953121	NM_003906.5(MCM3AP):c.3808G>A (p.Val1270Met)	MCM3AP (V1270M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1441725	NM_003906.5(MCM3AP):c.3799_3808del (p.Pro1267fs)	MCM3AP (P1267fs)	Microsatellite (frameshift variant)	not provided	GPathogenic
Select item 1532078	NM_003906.5(MCM3AP):c.3807C>T (p.Cys1269=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1917412	NM_003906.5(MCM3AP):c.3799C>T (p.Pro1267Ser)	MCM3AP (P1267S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1290381	NM_003906.5(MCM3AP):c.3798G>A (p.Ala1266=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1473009	NM_003906.5(MCM3AP):c.3797C>T (p.Ala1266Val)	MCM3AP (A1266V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1294838	NM_003906.5(MCM3AP):c.3795T>C (p.Ala1265=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1722115	NM_003906.5(MCM3AP):c.3791C>G (p.Pro1264Arg)	MCM3AP (P1264R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2795677	NM_003906.5(MCM3AP):c.3786T>C (p.Ala1262=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2135788	NM_003906.5(MCM3AP):c.3783G>A (p.Arg1261=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2067324	NM_003906.5(MCM3AP):c.3782G>T (p.Arg1261Leu)	MCM3AP (R1261L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1405885	NM_003906.5(MCM3AP):c.3780G>A (p.Met1260Ile)	MCM3AP (M1260I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1480782	NM_003906.5(MCM3AP):c.3773G>A (p.Arg1258His)	MCM3AP (R1258H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2163269	NM_003906.5(MCM3AP):c.3772C>T (p.Arg1258Cys)	MCM3AP (R1258C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1977753	NM_003906.5(MCM3AP):c.3765A>G (p.Lys1255=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1513625	NM_003906.5(MCM3AP):c.3761A>G (p.Lys1254Arg)	MCM3AP (K1254R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1981044	NM_003906.5(MCM3AP):c.3757C>T (p.Arg1253Cys)	MCM3AP (R1253C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2999756	NM_003906.5(MCM3AP):c.3753A>G (p.Thr1251=)	MCM3AP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1941199	NM_003906.5(MCM3AP):c.3752C>T (p.Thr1251Ile)	MCM3AP (T1251I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1329970	NM_003906.5(MCM3AP):c.3735-3C>A	MCM3AP	Single nucleotide variant (intron variant)	Inborn genetic diseases +2 more	GConflicting classifications of pathogenicity

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