ClinVar for Gene (Select 91351) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3081231	NM_001012967.3(DDX60L):c.947G>C (p.Arg316Pro)	DDX60L (R316P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081230	NM_001012967.3(DDX60L):c.689T>A (p.Phe230Tyr)	DDX60L (F230Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081229	NM_001012967.3(DDX60L):c.512A>G (p.Asn171Ser)	DDX60L (N171S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081228	NM_001012967.3(DDX60L):c.5116G>A (p.Glu1706Lys)	DDX60L (E1707K +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3081227	NM_001012967.3(DDX60L):c.4808C>G (p.Thr1603Ser)	DDX60L (T1603S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081226	NM_001012967.3(DDX60L):c.4798G>A (p.Val1600Ile)	DDX60L (V1600I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3081223	NM_001012967.3(DDX60L):c.4666C>A (p.Leu1556Ile)	DDX60L (L1556I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081222	NM_001012967.3(DDX60L):c.4574T>C (p.Leu1525Pro)	DDX60L (L1525P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081221	NM_001012967.3(DDX60L):c.4525T>G (p.Leu1509Val)	DDX60L (L1509V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081220	NM_001012967.3(DDX60L):c.4364G>T (p.Gly1455Val)	DDX60L (G1456V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081219	NM_001012967.3(DDX60L):c.4096C>T (p.Pro1366Ser)	DDX60L (P1367S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081218	NM_001012967.3(DDX60L):c.3944A>G (p.Gln1315Arg)	DDX60L (Q1315R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081217	NM_001012967.3(DDX60L):c.3852G>T (p.Met1284Ile)	DDX60L (M1284I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081216	NM_001012967.3(DDX60L):c.3775T>C (p.Phe1259Leu)	DDX60L (F1259L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3081214	NM_001012967.3(DDX60L):c.3605C>T (p.Thr1202Met)	DDX60L (T1202M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081213	NM_001012967.3(DDX60L):c.3556A>G (p.Ile1186Val)	DDX60L (I1187V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081212	NM_001012967.3(DDX60L):c.3503A>C (p.Asn1168Thr)	DDX60L (N1168T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081211	NM_001012967.3(DDX60L):c.3442T>C (p.Phe1148Leu)	DDX60L (F1148L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081210	NM_001012967.3(DDX60L):c.2926G>T (p.Asp976Tyr)	DDX60L (D976Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081209	NM_001012967.3(DDX60L):c.2785T>C (p.Cys929Arg)	DDX60L (C929R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081208	NM_001012967.3(DDX60L):c.2288T>C (p.Ile763Thr)	DDX60L (I763T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081207	NM_001012967.3(DDX60L):c.1562A>G (p.Gln521Arg)	DDX60L (Q521R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081206	NM_001012967.3(DDX60L):c.1306G>A (p.Glu436Lys)	DDX60L (E436K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081205	NM_001012967.3(DDX60L):c.1159G>T (p.Asp387Tyr)	DDX60L (D387Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081204	NM_001012967.3(DDX60L):c.1130G>A (p.Ser377Asn)	DDX60L (S377N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3081203	NM_001012967.3(DDX60L):c.1108G>C (p.Ala370Pro)	DDX60L (A370P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062804	GRCh37/hg19 4q27-35.2(chr4:123399154-190957473)x3	FAM149A, FAM218A +197 more	Copy number gain	not specified	GPathogenic
Select item 3062803	GRCh37/hg19 4q32.1-35.2(chr4:161589441-190957473)x1	AADAT, ACSL1 +85 more	Copy number loss	not specified	GPathogenic
Select item 3062774	GRCh37/hg19 4q32.3(chr4:169050575-169393595)x1	ANXA10, DDX60 +1 more	Copy number loss	not specified	GUncertain significance
Select item 3062767	GRCh37/hg19 4q24-35.2(chr4:101203509-190957473)x3	AADAT, ABCE1 +286 more	Copy number gain	not specified	GPathogenic
Select item 3024634	GRCh37/hg19 4q32.3-35.2(chr4:169060637-191154276)x1	AADAT, ACSL1 +68 more	Copy number loss	not provided	GPathogenic
Select item 3024631	GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	DDX60L, MTHFD2L +537 more	Copy number gain	not provided	GPathogenic
Select item 2853236	NM_001012967.3(DDX60L):c.3811-6del	DDX60L	Deletion (intron variant)	not provided	GBenign
Select item 2684399	GRCh37/hg19 4q32.3-35.2(chr4:167409608-190957473)x3	AADAT, ACSL1 +69 more	Copy number gain	not provided	GPathogenic
Select item 2655177	NM_001012967.3(DDX60L):c.3174A>G (p.Ala1058=)	DDX60L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2620695	NM_001012967.3(DDX60L):c.4426G>A (p.Gly1476Arg)	DDX60L (G1476R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619339	NM_001012967.3(DDX60L):c.4994A>T (p.Asp1665Val)	DDX60L (D1666V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2618895	NM_001012967.3(DDX60L):c.4870G>A (p.Ala1624Thr)	DDX60L (A1625T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618549	NM_001012967.3(DDX60L):c.1264T>A (p.Phe422Ile)	DDX60L (F422I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616219	NM_001012967.3(DDX60L):c.3484A>G (p.Lys1162Glu)	DDX60L (K1162E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613531	NM_001012967.3(DDX60L):c.1084G>C (p.Asp362His)	DDX60L (D362H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613207	NM_001012967.3(DDX60L):c.1321G>A (p.Val441Met)	DDX60L (V441M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612384	NM_001012967.3(DDX60L):c.1775C>G (p.Ser592Cys)	DDX60L (S592C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607155	NM_001012967.3(DDX60L):c.2768A>G (p.Lys923Arg)	DDX60L (K923R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598535	NM_001012967.3(DDX60L):c.2234A>C (p.Asn745Thr)	DDX60L (N745T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598289	NM_001012967.3(DDX60L):c.3017C>T (p.Thr1006Ile)	DDX60L (T1006I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596144	NM_001012967.3(DDX60L):c.3853C>T (p.Pro1285Ser)	DDX60L (P1286S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591308	NM_001012967.3(DDX60L):c.2665A>G (p.Ile889Val)	DDX60L (I889V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588143	NM_001012967.3(DDX60L):c.3530G>C (p.Arg1177Thr)	DDX60L (R1178T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559301	NM_001012967.3(DDX60L):c.4931T>C (p.Met1644Thr)	DDX60L (M1644T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555244	NM_001012967.3(DDX60L):c.587A>G (p.Asn196Ser)	DDX60L (N196S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553576	NM_001012967.3(DDX60L):c.3973G>C (p.Asp1325His)	DDX60L (D1325H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552114	NM_001012967.3(DDX60L):c.4976A>G (p.Asn1659Ser)	DDX60L (N1660S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550627	NM_001012967.3(DDX60L):c.1165A>G (p.Ile389Val)	DDX60L (I389V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546147	NM_001012967.3(DDX60L):c.544A>T (p.Thr182Ser)	DDX60L (T182S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544035	NM_001012967.3(DDX60L):c.4288G>A (p.Glu1430Lys)	DDX60L (E1430K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530624	NM_001012967.3(DDX60L):c.1771T>C (p.Phe591Leu)	DDX60L (F591L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525007	NM_001012967.3(DDX60L):c.2997C>A (p.Phe999Leu)	DDX60L (F999L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522463	NM_001012967.3(DDX60L):c.487A>T (p.Ile163Leu)	DDX60L (I163L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521432	NM_001012967.3(DDX60L):c.4859T>C (p.Met1620Thr)	DDX60L (M1621T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520810	NM_001012967.3(DDX60L):c.1589C>T (p.Ser530Leu)	DDX60L (S530L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518941	NM_001012967.3(DDX60L):c.3457G>C (p.Val1153Leu)	DDX60L (V1153L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514969	NM_001012967.3(DDX60L):c.3434G>C (p.Ser1145Thr)	DDX60L (S1145T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513098	NM_001012967.3(DDX60L):c.4795G>A (p.Gly1599Ser)	DDX60L (G1599S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512821	NM_001012967.3(DDX60L):c.2432G>A (p.Arg811His)	DDX60L (R811H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511309	NM_001012967.3(DDX60L):c.2291T>C (p.Val764Ala)	DDX60L (V764A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510777	NM_001012967.3(DDX60L):c.4088G>A (p.Gly1363Glu)	DDX60L (G1364E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495884	NM_001012967.3(DDX60L):c.4780A>T (p.Ile1594Phe)	DDX60L (I1595F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491923	NM_001012967.3(DDX60L):c.2914T>C (p.Ser972Pro)	DDX60L (S972P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463099	NM_001012967.3(DDX60L):c.1831T>G (p.Tyr611Asp)	DDX60L (Y611D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456091	NM_001012967.3(DDX60L):c.1664G>T (p.Gly555Val)	DDX60L (G555V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408550	NM_001012967.3(DDX60L):c.2699C>T (p.Thr900Ile)	DDX60L (T900I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401026	NM_001012967.3(DDX60L):c.2470G>A (p.Gly824Ser)	DDX60L (G824S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399155	NM_001012967.3(DDX60L):c.4043T>C (p.Leu1348Pro)	DDX60L (L1348P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390944	NM_001012967.3(DDX60L):c.4280A>G (p.His1427Arg)	DDX60L (H1428R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388260	NM_001012967.3(DDX60L):c.1305G>T (p.Leu435Phe)	DDX60L (L435F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377033	NM_001012967.3(DDX60L):c.1409C>T (p.Pro470Leu)	DDX60L (P470L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374734	NM_001012967.3(DDX60L):c.3126A>G (p.Ile1042Met)	DDX60L (I1042M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372742	NM_001012967.3(DDX60L):c.1173G>C (p.Arg391Ser)	DDX60L (R391S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370814	NM_001012967.3(DDX60L):c.2236G>T (p.Ala746Ser)	DDX60L (A746S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353966	NM_001012967.3(DDX60L):c.944C>T (p.Ser315Phe)	DDX60L (S315F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352836	NM_001012967.3(DDX60L):c.705G>C (p.Trp235Cys)	DDX60L (W235C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346397	NM_001012967.3(DDX60L):c.239G>A (p.Gly80Glu)	DDX60L (G80E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338971	NM_001012967.3(DDX60L):c.1904C>A (p.Ala635Glu)	DDX60L (A635E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323729	NM_001012967.3(DDX60L):c.2140G>A (p.Gly714Arg)	DDX60L (G714R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321483	NM_001012967.3(DDX60L):c.3554A>G (p.Tyr1185Cys)	DDX60L (Y1185C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317805	NM_001012967.3(DDX60L):c.1384T>A (p.Leu462Met)	DDX60L (L462M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310963	NM_001012967.3(DDX60L):c.3634G>C (p.Glu1212Gln)	DDX60L (E1213Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295385	NM_001012967.3(DDX60L):c.4349A>C (p.Lys1450Thr)	DDX60L, LOC132089087 (K1450T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294112	NM_001012967.3(DDX60L):c.346A>G (p.Asn116Asp)	DDX60L (N116D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293994	NM_001012967.3(DDX60L):c.4501C>G (p.Leu1501Val)	DDX60L (L1501V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290706	NM_001012967.3(DDX60L):c.2929G>A (p.Asp977Asn)	DDX60L (D977N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289585	NM_001012967.3(DDX60L):c.2077A>G (p.Asn693Asp)	DDX60L (N693D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288721	NM_001012967.3(DDX60L):c.4743T>A (p.Asp1581Glu)	DDX60L (D1582E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285435	NM_001012967.3(DDX60L):c.3863C>G (p.Ser1288Cys)	DDX60L (S1289C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282449	NM_001012967.3(DDX60L):c.1791G>A (p.Met597Ile)	DDX60L (M597I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279974	NM_001012967.3(DDX60L):c.5110C>A (p.His1704Asn)	DDX60L (H1705N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276351	NM_001012967.3(DDX60L):c.1499T>C (p.Ile500Thr)	DDX60L (I500T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2247056	NM_001012967.3(DDX60L):c.2255T>G (p.Leu752Arg)	DDX60L (L752R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219931	NM_001012967.3(DDX60L):c.770C>T (p.Ser257Leu)	DDX60L (S257L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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