"Illumina Laboratory Services, Illumina"[submitter] AND "FLNB"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 902083	NM_001457.3(FLNB):c.-160C>G	FLNB	Single nucleotide variant	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 902084	NM_001457.3(FLNB):c.-145G>T	FLNB	Single nucleotide variant	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 346290	NM_001457.4(FLNB):c.-131G>C	FLNB	Single nucleotide variant (5 prime UTR variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 346291	NM_001457.4(FLNB):c.-107T>G	FLNB	Single nucleotide variant (5 prime UTR variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 346292	NM_001457.4(FLNB):c.-103A>G	FLNB	Single nucleotide variant (5 prime UTR variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 902963	NM_001457.4(FLNB):c.-97C>T	FLNB	Single nucleotide variant (5 prime UTR variant)	FLNB-Related Spectrum Disorders	GLikely benign
Select item 346293	NM_001457.4(FLNB):c.-95C>G	FLNB	Single nucleotide variant (5 prime UTR variant)	FLNB-Related Spectrum Disorders	GLikely benign
Select item 902964	NM_001457.4(FLNB):c.-88C>A	FLNB	Single nucleotide variant (5 prime UTR variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 346294	NM_001457.4(FLNB):c.-81G>C	FLNB	Single nucleotide variant (5 prime UTR variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 346295	NM_001457.4(FLNB):c.-76C>A	FLNB	Single nucleotide variant (5 prime UTR variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 346296	NM_001457.4(FLNB):c.-31C>T	FLNB	Single nucleotide variant (5 prime UTR variant)	FLNB-Related Spectrum Disorders +2 more	GBenign
Select item 346297	NM_001457.4(FLNB):c.-4C>T	FLNB	Single nucleotide variant (5 prime UTR variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 516180	NM_001457.4(FLNB):c.9A>G (p.Val3=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-related condition +3 more	GConflicting classifications of pathogenicity
Select item 900408	NM_001457.4(FLNB):c.187T>C (p.Tyr63His)	FLNB (Y63H)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +1 more	GUncertain significance
Select item 346298	NM_001457.4(FLNB):c.233A>G (p.Glu78Gly)	FLNB (E78G)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +1 more	GUncertain significance
Select item 900409	NM_001457.4(FLNB):c.247G>T (p.Ala83Ser)	FLNB (A83S)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 346299	NM_001457.4(FLNB):c.249G>A (p.Ala83=)	FLNB	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 258103	NM_001457.4(FLNB):c.292+8C>A	FLNB	Single nucleotide variant (intron variant)	Spondylocarpotarsal synostosis syndrome +8 more	GBenign/Likely benign
Select item 379652	NM_001457.4(FLNB):c.292+12G>C	FLNB	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 258102	NM_001457.4(FLNB):c.292+14C>G	FLNB	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 736702	NM_001457.4(FLNB):c.420G>A (p.Thr140=)	FLNB	Single nucleotide variant (synonymous variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 346300	NM_001457.4(FLNB):c.544C>T (p.Leu182=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 900476	NM_001457.4(FLNB):c.563C>G (p.Ser188Cys)	FLNB (S188C)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +1 more	GUncertain significance
Select item 258118	NM_001457.4(FLNB):c.669G>A (p.Pro223=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +2 more	GBenign/Likely benign
Select item 508835	NM_001457.4(FLNB):c.762G>A (p.Pro254=)	FLNB	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 346301	NM_001457.4(FLNB):c.776C>T (p.Ala259Val)	FLNB (A259V)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +3 more	GUncertain significance
Select item 346302	NM_001457.4(FLNB):c.792C>T (p.Ile264=)	FLNB	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 902143	NM_001457.4(FLNB):c.798C>T (p.Pro266=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +1 more	GConflicting classifications of pathogenicity
Select item 252548	NM_001457.4(FLNB):c.808A>G (p.Met270Val)	FLNB (M270V)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +9 more	GConflicting classifications of pathogenicity
Select item 346303	NM_001457.4(FLNB):c.825C>T (p.Ala275=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +1 more	GConflicting classifications of pathogenicity
Select item 346304	NM_001457.4(FLNB):c.852C>T (p.Ala284=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-related condition +2 more	GConflicting classifications of pathogenicity
Select item 346305	NM_001457.4(FLNB):c.853G>A (p.Gly285Arg)	FLNB (G285R)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 902144	NM_001457.4(FLNB):c.864C>A (p.Asp288Glu)	FLNB (D288E)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 631929	NM_001457.4(FLNB):c.864_865insT (p.Val289fs)	FLNB (V289fs)	Insertion (frameshift variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 346306	NM_001457.4(FLNB):c.864C>T (p.Asp288=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-related condition +3 more	GConflicting classifications of pathogenicity
Select item 346307	NM_001457.4(FLNB):c.865G>A (p.Val289Met)	FLNB (V289M)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 258123	NM_001457.4(FLNB):c.927T>C (p.Ser309=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +2 more	GBenign
Select item 497262	NM_001457.4(FLNB):c.1044C>T (p.Asp348=)	FLNB	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 903022	NM_001457.4(FLNB):c.1148-8T>G	FLNB	Single nucleotide variant (intron variant)	FLNB-Related Spectrum Disorders +1 more	GConflicting classifications of pathogenicity
Select item 903023	NM_001457.4(FLNB):c.1186C>T (p.Pro396Ser)	FLNB (P396S)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 449801	NM_001457.4(FLNB):c.1196A>G (p.Lys399Arg)	FLNB (K399R)	Single nucleotide variant (missense variant)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 346308	NM_001457.4(FLNB):c.1278C>T (p.His426=)	FLNB	Single nucleotide variant (synonymous variant)	Connective tissue disorder +2 more	GBenign/Likely benign
Select item 346309	NM_001457.4(FLNB):c.1290C>G (p.Ile430Met)	FLNB (I430M)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 899410	NM_001457.4(FLNB):c.1327G>A (p.Val443Ile)	FLNB (V443I)	Single nucleotide variant (missense variant)	FLNB-related condition +3 more	GConflicting classifications of pathogenicity
Select item 810979	NM_001457.4(FLNB):c.1327G>C (p.Val443Leu)	FLNB (V443L)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GConflicting classifications of pathogenicity
Select item 899411	NM_001457.4(FLNB):c.1367G>A (p.Arg456Gln)	FLNB (R456Q)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +2 more	GConflicting classifications of pathogenicity
Select item 346310	NM_001457.4(FLNB):c.1373G>A (p.Ser458Asn)	FLNB (S458N)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 346311	NM_001457.4(FLNB):c.1384C>T (p.Leu462=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-related condition +2 more	GConflicting classifications of pathogenicity
Select item 346312	NM_001457.4(FLNB):c.1409G>A (p.Arg470Gln)	FLNB (R470Q)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +1 more	GConflicting classifications of pathogenicity
Select item 899412	NM_001457.4(FLNB):c.1451G>C (p.Ser484Thr)	FLNB (S484T)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +1 more	GConflicting classifications of pathogenicity
Select item 389036	NM_001457.4(FLNB):c.1534G>A (p.Ala512Thr)	FLNB (A512T)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +2 more	GConflicting classifications of pathogenicity
Select item 193630	NM_001457.4(FLNB):c.1559C>T (p.Pro520Leu)	FLNB (P520L)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 900529	NM_001457.4(FLNB):c.1583C>T (p.Thr528Ile)	FLNB (T528I)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 258099	NM_001457.4(FLNB):c.1611-4G>A	FLNB	Single nucleotide variant (intron variant)	FLNB-Related Spectrum Disorders +3 more	GBenign
Select item 346313	NM_001457.4(FLNB):c.1628T>C (p.Val543Ala)	FLNB (V543A)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 810892	NM_001457.4(FLNB):c.1640C>T (p.Ala547Val)	FLNB (A547V)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 346314	NM_001457.4(FLNB):c.1688T>C (p.Ile563Thr)	FLNB (I563T)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +2 more	GConflicting classifications of pathogenicity
Select item 900530	NM_001457.4(FLNB):c.1692C>T (p.Val564=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +1 more	GConflicting classifications of pathogenicity
Select item 900531	NM_001457.4(FLNB):c.1697G>A (p.Arg566Gln)	FLNB (R566Q)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 346315	NM_001457.4(FLNB):c.1748-5C>G	FLNB	Single nucleotide variant (intron variant)	FLNB-Related Spectrum Disorders +1 more	GConflicting classifications of pathogenicity
Select item 218523	NM_001457.4(FLNB):c.1868A>T (p.Asp623Val)	FLNB (D623V)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 258100	NM_001457.4(FLNB):c.1869C>T (p.Asp623=)	FLNB	Single nucleotide variant (synonymous variant)	Connective tissue disorder +3 more	GBenign
Select item 346316	NM_001457.4(FLNB):c.1919C>T (p.Thr640Met)	FLNB (T640M)	Single nucleotide variant (missense variant)	not specified +8 more	GBenign/Likely benign
Select item 288568	NM_001457.4(FLNB):c.1946G>A (p.Arg649Gln)	FLNB (R649Q)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 709969	NM_001457.4(FLNB):c.1998C>T (p.Ala666=)	FLNB	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 346317	NM_001457.4(FLNB):c.2035C>T (p.Pro679Ser)	FLNB (P679S)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +1 more	GConflicting classifications of pathogenicity
Select item 346318	NM_001457.4(FLNB):c.2055+4A>G	FLNB	Single nucleotide variant (intron variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 902192	NM_001457.4(FLNB):c.2059G>A (p.Gly687Arg)	FLNB (G687R)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +1 more	GConflicting classifications of pathogenicity
Select item 903074	NM_001457.4(FLNB):c.2084A>G (p.Gln695Arg)	FLNB (Q695R)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 346319	NM_001457.4(FLNB):c.2097G>C (p.Arg699=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 903075	NM_001457.4(FLNB):c.2104G>A (p.Gly702Ser)	FLNB (G702S)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 903076	NM_001457.4(FLNB):c.2130G>C (p.Pro710=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-related condition +2 more	GConflicting classifications of pathogenicity
Select item 346320	NM_001457.4(FLNB):c.2136G>A (p.Lys712=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +1 more	GConflicting classifications of pathogenicity
Select item 346321	NM_001457.4(FLNB):c.2187C>T (p.His729=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +1 more	GConflicting classifications of pathogenicity
Select item 989333	NM_001457.4(FLNB):c.2297C>T (p.Thr766Met)	FLNB (T766M)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 346322	NM_001457.4(FLNB):c.2382C>T (p.Asp794=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +2 more	GBenign/Likely benign
Select item 388816	NM_001457.4(FLNB):c.2453G>A (p.Arg818Gln)	FLNB (R818Q)	Single nucleotide variant (missense variant)	FLNB-related condition +2 more	GConflicting classifications of pathogenicity
Select item 284044	NM_001457.4(FLNB):c.2493C>T (p.Pro831=)	FLNB, LOC129936935	Single nucleotide variant (synonymous variant)	Connective tissue disorder +3 more	GBenign/Likely benign
Select item 899450	NM_001457.4(FLNB):c.2516T>G (p.Val839Gly)	FLNB, LOC129936935 (V839G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 346323	NM_001457.4(FLNB):c.2523T>G (p.Pro841=)	FLNB, LOC129936935	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +7 more	GBenign/Likely benign
Select item 346324	NM_001457.4(FLNB):c.2529C>T (p.His843=)	FLNB, LOC129936935	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +1 more	GConflicting classifications of pathogenicity
Select item 346325	NM_001457.4(FLNB):c.2575+12C>T	FLNB, LOC129936935	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 899451	NM_001457.4(FLNB):c.2643C>T (p.Asn881=)	FLNB	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 439739	NM_001457.4(FLNB):c.2644G>C (p.Val882Leu)	FLNB (V882L)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +2 more	GConflicting classifications of pathogenicity
Select item 194935	NM_001457.4(FLNB):c.2773G>T (p.Gly925Cys)	FLNB (G925C)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +2 more	GConflicting classifications of pathogenicity
Select item 900578	NM_001457.4(FLNB):c.2804C>T (p.Thr935Ile)	FLNB (T935I)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 900579	NM_001457.4(FLNB):c.2864-5T>A	FLNB	Single nucleotide variant (intron variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 346326	NM_001457.4(FLNB):c.2907G>A (p.Arg969=)	FLNB	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 346327	NM_001457.4(FLNB):c.2908G>A (p.Gly970Arg)	FLNB (G970R)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders	GUncertain significance
Select item 346328	NM_001457.4(FLNB):c.2931G>A (p.Leu977=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +2 more	GBenign/Likely benign
Select item 346329	NM_001457.4(FLNB):c.2935G>A (p.Val979Met)	FLNB (V979M)	Single nucleotide variant (missense variant)	FLNB-related condition +3 more	GConflicting classifications of pathogenicity
Select item 900580	NM_001457.4(FLNB):c.3052G>A (p.Val1018Met)	FLNB (V1018M)	Single nucleotide variant (missense variant)	FLNB-related condition +3 more	GConflicting classifications of pathogenicity
Select item 195475	NM_001457.4(FLNB):c.3090C>T (p.Tyr1030=)	FLNB	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 346330	NM_001457.4(FLNB):c.3138C>T (p.His1046=)	FLNB	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 386687	NM_001457.4(FLNB):c.3169A>C (p.Lys1057Gln)	FLNB (K1057Q)	Single nucleotide variant (missense variant)	FLNB-related condition +3 more	GConflicting classifications of pathogenicity
Select item 346331	NM_001457.4(FLNB):c.3240G>A (p.Pro1080=)	FLNB	Single nucleotide variant (synonymous variant)	not specified +4 more	GBenign/Likely benign
Select item 593766	NM_001457.4(FLNB):c.3264C>T (p.Ser1088=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +3 more	GBenign/Likely benign
Select item 902265	NM_001457.4(FLNB):c.3287C>T (p.Ser1096Phe)	FLNB (S1096F)	Single nucleotide variant (missense variant)	FLNB-Related Spectrum Disorders +1 more	GUncertain significance
Select item 285500	NM_001457.4(FLNB):c.3288C>T (p.Ser1096=)	FLNB	Single nucleotide variant (synonymous variant)	FLNB-Related Spectrum Disorders +2 more	GConflicting classifications of pathogenicity
Select item 902266	NM_001457.4(FLNB):c.3289G>A (p.Val1097Ile)	FLNB (V1097I)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity

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