C3469542[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1026620	NM_032444.4(SLX4):c.5497C>T (p.Arg1833Trp)	SLX4 (R1833W)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 574625	NM_032444.4(SLX4):c.5480del (p.Gly1827fs)	SLX4 (G1827fs)	Deletion (frameshift variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 407929	NM_032444.4(SLX4):c.5477G>A (p.Arg1826Gln)	SLX4 (R1826Q)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 1336585	NM_032444.4(SLX4):c.5476C>T (p.Arg1826Trp)	SLX4 (R1826W)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 407914	NM_032444.4(SLX4):c.5467C>T (p.Arg1823Trp)	SLX4 (R1823W)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 456337	NM_032444.4(SLX4):c.5441G>A (p.Arg1814His)	SLX4 (R1814H)	Single nucleotide variant (missense variant)	Fanconi anemia +2 more	GUncertain significance
Select item 929618	NM_032444.4(SLX4):c.5440C>T (p.Arg1814Cys)	SLX4 (R1814C)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 701209	NM_032444.4(SLX4):c.5433C>T (p.Ala1811=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +1 more	GLikely benign
Select item 690302	NM_032444.4(SLX4):c.5413T>C (p.Cys1805Arg)	SLX4 (C1805R)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 1417020	NM_032444.4(SLX4):c.5410C>T (p.His1804Tyr)	SLX4 (H1804Y)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 407900	NM_032444.4(SLX4):c.5404G>A (p.Asp1802Asn)	SLX4 (D1802N)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 526497	NM_032444.4(SLX4):c.5403G>C (p.Leu1801=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +2 more	GLikely benign
Select item 997508	NM_032444.4(SLX4):c.5383C>T (p.Arg1795Cys)	SLX4 (R1795C)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 526486	NM_032444.4(SLX4):c.5382G>A (p.Ser1794=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +1 more	GLikely benign
Select item 526388	NM_032444.4(SLX4):c.5336G>A (p.Arg1779Gln)	SLX4 (R1779Q)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 526426	NM_032444.4(SLX4):c.5304G>C (p.Gln1768His)	SLX4 (Q1768H)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 1432851	NM_032444.4(SLX4):c.5291C>T (p.Pro1764Leu)	SLX4 (P1764L)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 414716	NM_032444.4(SLX4):c.5259C>T (p.Asp1753=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +1 more	GBenign
Select item 241695	NM_032444.4(SLX4):c.5248_5249delinsTT (p.Ala1750Leu)	SLX4 (A1750L)	Indel (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 864196	NM_032444.4(SLX4):c.5242C>T (p.Gln1748Ter)	SLX4 (Q1748*)	Single nucleotide variant (nonsense)	Fanconi anemia +1 more	GUncertain significance
Select item 456334	NM_032444.4(SLX4):c.5229G>A (p.Ser1743=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +1 more	GLikely benign
Select item 1371379	NM_032444.4(SLX4):c.5228C>T (p.Ser1743Leu)	SLX4 (S1743L)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 1434387	NM_032444.4(SLX4):c.5223T>G (p.Ser1741Arg)	SLX4 (S1741R)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 779499	NM_032444.4(SLX4):c.5214G>A (p.Gly1738=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +1 more	GLikely benign
Select item 848629	NM_032444.4(SLX4):c.5212G>T (p.Gly1738Trp)	SLX4 (G1738W)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 1370356	NM_032444.4(SLX4):c.5208C>T (p.Gly1736=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 456332	NM_032444.4(SLX4):c.5188T>C (p.Ser1730Pro)	SLX4 (S1730P)	Single nucleotide variant (missense variant)	Fanconi anemia +2 more	GUncertain significance
Select item 1361466	NM_032444.4(SLX4):c.5185G>C (p.Glu1729Gln)	SLX4 (E1729Q)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 407918	NM_032444.4(SLX4):c.5153+6C>A	SLX4	Single nucleotide variant (intron variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 966193	NM_032444.4(SLX4):c.5144G>A (p.Ser1715Asn)	SLX4 (S1715N)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1401141	NM_032444.4(SLX4):c.5141T>G (p.Leu1714Trp)	SLX4 (L1714W)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 573413	NM_032444.4(SLX4):c.5072A>G (p.Asn1691Ser)	SLX4 (N1691S)	Single nucleotide variant (missense variant)	Fanconi anemia +2 more	GUncertain significance
Select item 319144	NM_032444.4(SLX4):c.5060C>G (p.Pro1687Arg)	SLX4 (P1687R)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 526390	NM_032444.4(SLX4):c.5040G>C (p.Arg1680Ser)	SLX4 (R1680S)	Single nucleotide variant (missense variant)	Fanconi anemia +3 more	GUncertain significance
Select item 212220	NM_032444.4(SLX4):c.5029C>T (p.Pro1677Ser)	SLX4 (P1677S)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 1054622	NM_032444.4(SLX4):c.4960C>T (p.His1654Tyr)	SLX4 (H1654Y)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 1043341	NM_032444.4(SLX4):c.4927G>T (p.Ala1643Ser)	SLX4 (A1643S)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1692018	NM_032444.4(SLX4):c.4903A>G (p.Lys1635Glu)	SLX4 (K1635E)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 887098	NM_032444.4(SLX4):c.4892C>T (p.Ser1631Phe)	SLX4 (S1631F)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 948293	NM_032444.4(SLX4):c.4873C>T (p.His1625Tyr)	SLX4 (H1625Y)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 1477344	NM_032444.4(SLX4):c.4871C>T (p.Pro1624Leu)	SLX4 (P1624L)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 526418	NM_032444.4(SLX4):c.4856C>T (p.Pro1619Leu)	SLX4 (P1619L)	Single nucleotide variant (missense variant)	Fanconi anemia +2 more	GUncertain significance
Select item 414719	NM_032444.4(SLX4):c.4836C>T (p.Asp1612=)	SLX4	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 1668806	NM_032444.4(SLX4):c.4824A>G (p.Ser1608=)	SLX4	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 935208	NM_032444.4(SLX4):c.4822T>G (p.Ser1608Ala)	SLX4 (S1608A)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 1051899	NM_032444.4(SLX4):c.4768C>G (p.Gln1590Glu)	SLX4 (Q1590E)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +2 more	GUncertain significance
Select item 968611	NM_032444.4(SLX4):c.4766G>A (p.Arg1589His)	SLX4 (R1589H)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 456329	NM_032444.4(SLX4):c.4765C>T (p.Arg1589Cys)	SLX4 (R1589C)	Single nucleotide variant (missense variant)	Fanconi anemia +2 more	GConflicting classifications of pathogenicity
Select item 319149	NM_032444.4(SLX4):c.4750C>T (p.Arg1584Cys)	SLX4 (R1584C)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 1577591	NM_032444.4(SLX4):c.4740-5G>A	SLX4	Single nucleotide variant (intron variant)	Fanconi anemia complementation group P +1 more	GLikely benign
Select item 1022734	NM_032444.4(SLX4):c.4715C>T (p.Pro1572Leu)	SLX4 (P1572L)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 1343303	NM_032444.4(SLX4):c.4712C>T (p.Thr1571Met)	SLX4 (T1571M)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 807969	NM_032444.4(SLX4):c.4682C>T (p.Thr1561Met)	SLX4 (T1561M)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 947391	NM_032444.4(SLX4):c.4658A>T (p.Asn1553Ile)	SLX4 (N1553I)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 319150	NM_032444.4(SLX4):c.4650GAA[2] (p.Lys1552del)	SLX4 (K1552del)	Microsatellite (inframe_deletion)	Fanconi anemia +1 more	GUncertain significance
Select item 860423	NM_032444.4(SLX4):c.4649G>A (p.Arg1550Gln)	SLX4 (R1550Q)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 1629760	NM_032444.4(SLX4):c.4599T>C (p.Ala1533=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +1 more	GLikely benign
Select item 436791	NM_032444.4(SLX4):c.4580C>T (p.Pro1527Leu)	SLX4 (P1527L)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 319151	NM_032444.4(SLX4):c.4546G>A (p.Gly1516Arg)	SLX4 (G1516R)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +2 more	GUncertain significance
Select item 526484	NM_032444.4(SLX4):c.4545C>T (p.Asp1515=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia +2 more	GLikely benign
Select item 1035729	NM_032444.4(SLX4):c.4481_4525del (p.Gly1494_Ser1508del)	SLX4	Deletion (inframe_deletion)	not provided +2 more	GUncertain significance
Select item 1365733	NM_032444.4(SLX4):c.4523C>T (p.Ser1508Leu)	SLX4 (S1508L)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 1023165	NM_032444.4(SLX4):c.4508C>T (p.Pro1503Leu)	SLX4 (P1503L)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 658057	NM_032444.4(SLX4):c.4484C>T (p.Ala1495Val)	SLX4 (A1495V)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 414717	NM_032444.4(SLX4):c.4456A>C (p.Arg1486=)	SLX4	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 1421269	NM_032444.4(SLX4):c.4443C>G (p.Ser1481Arg)	SLX4 (S1481R)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 241691	NM_032444.4(SLX4):c.4427C>G (p.Thr1476Ser)	SLX4 (T1476S)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 885261	NM_032444.4(SLX4):c.4409C>T (p.Pro1470Leu)	SLX4 (P1470L)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 645501	NM_032444.4(SLX4):c.4403G>A (p.Arg1468His)	SLX4 (R1468H)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 944878	NM_032444.4(SLX4):c.4393C>T (p.Arg1465Cys)	SLX4 (R1465C)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 1017644	NM_032444.4(SLX4):c.4390A>G (p.Ser1464Gly)	SLX4 (S1464G)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 456325	NM_032444.4(SLX4):c.4387G>A (p.Asp1463Asn)	SLX4 (D1463N)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 436778	NM_032444.4(SLX4):c.4384G>T (p.Ala1462Ser)	SLX4 (A1462S)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 654173	NM_032444.4(SLX4):c.4378G>A (p.Glu1460Lys)	SLX4 (E1460K)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 1319486	NM_032444.4(SLX4):c.4367G>A (p.Arg1456His)	SLX4 (R1456H)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1476491	NM_032444.4(SLX4):c.4355G>A (p.Ser1452Asn)	SLX4 (S1452N)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +2 more	GUncertain significance
Select item 698488	NM_032444.4(SLX4):c.4344C>T (p.Pro1448=)	SLX4	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 697201	NM_032444.4(SLX4):c.4335G>C (p.Arg1445=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +1 more	GLikely benign
Select item 1473151	NM_032444.4(SLX4):c.4334G>A (p.Arg1445Gln)	SLX4 (R1445Q)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 407904	NM_032444.4(SLX4):c.4333C>T (p.Arg1445Trp)	SLX4 (R1445W)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 407923	NM_032444.4(SLX4):c.4301C>T (p.Ser1434Leu)	SLX4 (S1434L)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 1417300	NM_032444.4(SLX4):c.4268T>C (p.Ile1423Thr)	SLX4 (I1423T)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 456321	NM_032444.4(SLX4):c.4267A>G (p.Ile1423Val)	SLX4 (I1423V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GConflicting classifications of pathogenicity
Select item 1470938	NM_032444.4(SLX4):c.4250G>A (p.Ser1417Asn)	SLX4 (S1417N)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 645466	NM_032444.4(SLX4):c.4186G>A (p.Gly1396Arg)	SLX4 (G1396R)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 1587607	NM_032444.4(SLX4):c.4185C>T (p.Val1395=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +1 more	GLikely benign
Select item 1467692	NM_032444.4(SLX4):c.4146C>A (p.Ser1382Arg)	SLX4 (S1382R)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 855511	NM_032444.4(SLX4):c.4144A>G (p.Ser1382Gly)	SLX4 (S1382G)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GUncertain significance
Select item 929605	NM_032444.4(SLX4):c.4089_4090del (p.Asp1365fs)	SLX4 (D1365fs)	Deletion (frameshift variant)	Fanconi anemia complementation group P +2 more	GPathogenic/Likely pathogenic
Select item 235267	NM_032444.4(SLX4):c.4046G>C (p.Gly1349Ala)	SLX4 (G1349A)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 456318	NM_032444.4(SLX4):c.4034G>A (p.Arg1345His)	SLX4 (R1345H)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 803197	NM_032444.4(SLX4):c.4021A>G (p.Arg1341Gly)	SLX4 (R1341G)	Single nucleotide variant (missense variant)	Fanconi anemia +2 more	GUncertain significance
Select item 862622	NM_032444.4(SLX4):c.4019A>G (p.His1340Arg)	SLX4 (H1340R)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 1018470	NM_032444.4(SLX4):c.4002C>A (p.Asp1334Glu)	SLX4 (D1334E)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 456317	NM_032444.4(SLX4):c.3962C>T (p.Pro1321Leu)	SLX4 (P1321L)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +2 more	GUncertain significance
Select item 1059776	NM_032444.4(SLX4):c.3950C>T (p.Pro1317Leu)	SLX4 (P1317L)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 319154	NM_032444.4(SLX4):c.3940C>A (p.Gln1314Lys)	SLX4 (Q1314K)	Single nucleotide variant (missense variant)	Fanconi anemia +3 more	GUncertain significance
Select item 456316	NM_032444.4(SLX4):c.3926C>T (p.Ser1309Phe)	SLX4 (S1309F)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 861138	NM_032444.4(SLX4):c.3919_3921del (p.Lys1307del)	SLX4 (K1307del)	Deletion (inframe_deletion)	Fanconi anemia complementation group P +1 more	GUncertain significance
Select item 1070771	NM_032444.4(SLX4):c.3895_3896del (p.Arg1299fs)	SLX4 (R1299fs)	Deletion (frameshift variant)	Fanconi anemia +1 more	GPathogenic/Likely pathogenic

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