ClinVar for Gene (Select 54443) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3379748	NM_018685.5(ANLN):c.1271C>T (p.Ala424Val)	ANLN (A424V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3354461	NM_018685.5(ANLN):c.2055A>G (p.Glu685=)	ANLN	Single nucleotide variant (synonymous variant)	ANLN-related disorder	GLikely benign
Select item 3349691	NM_018685.5(ANLN):c.3078+10A>G	ANLN	Single nucleotide variant (intron variant)	ANLN-related disorder	GLikely benign
Select item 3349132	NM_018685.5(ANLN):c.2559C>G (p.Asn853Lys)	ANLN (N815K +2 more)	Single nucleotide variant (missense variant)	ANLN-related disorder	GUncertain significance
Select item 3298631	NM_018685.5(ANLN):c.1207A>C (p.Asn403His)	ANLN (N403H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298624	NM_018685.5(ANLN):c.1987G>A (p.Gly663Ser)	ANLN (G626S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298623	NM_018685.5(ANLN):c.2017A>C (p.Ile673Leu)	ANLN (I673L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298621	NM_018685.5(ANLN):c.205A>G (p.Lys69Glu)	ANLN (K69E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298620	NM_018685.5(ANLN):c.740G>A (p.Arg247Lys)	ANLN (R247K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298619	NM_018685.5(ANLN):c.2088G>T (p.Lys696Asn)	ANLN (K658N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127060	NM_018685.5(ANLN):c.997A>G (p.Ile333Val)	ANLN (I333V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127059	NM_018685.5(ANLN):c.914A>G (p.Asp305Gly)	ANLN (D305G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127058	NM_018685.5(ANLN):c.755G>A (p.Ser252Asn)	ANLN (S252N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127057	NM_018685.5(ANLN):c.44G>C (p.Arg15Thr)	ANLN (R15T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127056	NM_018685.5(ANLN):c.1643G>A (p.Arg548His)	ANLN (R510H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127055	NM_018685.5(ANLN):c.1542G>A (p.Met514Ile)	ANLN (M514I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3127053	NM_018685.5(ANLN):c.1266T>G (p.His422Gln)	ANLN (H422Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127052	NM_018685.5(ANLN):c.1216G>C (p.Ala406Pro)	ANLN (A406P)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 3123932	NM_001100425.2(MATCAP2):c.49C>A (p.Arg17Ser)	ANLN, MATCAP2 (R17S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3068300	NM_018685.5(ANLN):c.3010C>T (p.Arg1004Ter)	ANLN (R1004* +2 more)	Single nucleotide variant (nonsense)	Focal segmental glomerulosclerosis 8	GUncertain significance
Select item 3062981	GRCh37/hg19 7p14.3-14.1(chr7:33478398-39686397)x1	AMPH, ANLN +22 more	Copy number loss	not specified	GLikely pathogenic
Select item 3054444	NM_018685.5(ANLN):c.9G>C (p.Pro3=)	MATCAP2, ANLN (R14G)	Single nucleotide variant (missense variant +1 more)	ANLN-related disorder	GLikely benign
Select item 3031106	NM_018685.5(ANLN):c.2528T>C (p.Met843Thr)	ANLN (M805T +2 more)	Single nucleotide variant (missense variant)	ANLN-related disorder	GUncertain significance
Select item 3030756	NM_018685.5(ANLN):c.873+9G>C	ANLN	Single nucleotide variant (intron variant)	ANLN-related disorder	GLikely benign
Select item 3030153	NM_018685.5(ANLN):c.1288-10A>T	ANLN	Single nucleotide variant (intron variant)	ANLN-related disorder	GLikely benign
Select item 3026006	NM_018685.5(ANLN):c.795C>T (p.Gly265=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3023836	NM_018685.5(ANLN):c.3072A>G (p.Lys1024=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3020398	NM_018685.5(ANLN):c.1605A>G (p.Thr535=)	ANLN	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3019572	NM_018685.5(ANLN):c.880A>G (p.Thr294Ala)	ANLN (T294A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3007420	NM_018685.5(ANLN):c.80C>T (p.Pro27Leu)	ANLN (P27L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3000093	NM_018685.5(ANLN):c.336C>A (p.Thr112=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2994483	NM_018685.5(ANLN):c.1024G>T (p.Val342Phe)	ANLN (V342F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2990564	NM_018685.5(ANLN):c.2015+10T>C	ANLN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2987826	NM_018685.5(ANLN):c.1540A>G (p.Met514Val)	ANLN (M514V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2985290	NM_018685.5(ANLN):c.2583A>G (p.Thr861=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2983888	NM_018685.5(ANLN):c.1480G>A (p.Glu494Lys)	ANLN (E494K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2983005	NM_018685.5(ANLN):c.230T>A (p.Val77Glu)	ANLN (V77E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2982701	NM_018685.5(ANLN):c.2300-17T>C	ANLN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2976216	NM_018685.5(ANLN):c.3232G>C (p.Asp1078His)	ANLN (D1041H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2975734	NM_018685.5(ANLN):c.235G>T (p.Val79Phe)	ANLN (V79F)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2974812	NM_018685.5(ANLN):c.488-18_488-17del	ANLN	Deletion (intron variant)	not provided	GLikely benign
Select item 2968702	NM_018685.5(ANLN):c.879T>C (p.Ala293=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2963835	NM_018685.5(ANLN):c.1618G>A (p.Val540Ile)	ANLN (V540I)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2961354	NM_018685.5(ANLN):c.548C>T (p.Pro183Leu)	ANLN (P183L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2961079	NM_018685.5(ANLN):c.1172G>A (p.Arg391His)	ANLN (R391H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2918981	NM_018685.5(ANLN):c.851A>G (p.Asn284Ser)	ANLN (N284S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2908444	NM_018685.5(ANLN):c.1412G>A (p.Ser471Asn)	ANLN (S471N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2897844	NM_018685.5(ANLN):c.38G>A (p.Arg13His)	ANLN (R13H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2891918	NM_018685.5(ANLN):c.2057G>A (p.Arg686His)	ANLN (R649H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2885011	NM_018685.5(ANLN):c.448G>T (p.Ala150Ser)	ANLN (A150S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2880191	NM_018685.5(ANLN):c.224C>T (p.Thr75Ile)	ANLN (T75I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2873237	NM_018685.5(ANLN):c.2720C>G (p.Pro907Arg)	ANLN (P907R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2862828	NM_018685.5(ANLN):c.3028T>A (p.Ser1010Thr)	ANLN (S1010T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2856981	NM_018685.5(ANLN):c.2748+6_2748+7dup	ANLN	Duplication (intron variant)	not provided	GLikely benign
Select item 2846674	NM_018685.5(ANLN):c.1097-18TG[3]	ANLN	Microsatellite (intron variant)	not provided	GBenign
Select item 2839714	NM_018685.5(ANLN):c.824C>T (p.Ser275Leu)	ANLN (S275L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2824137	NM_018685.5(ANLN):c.747T>C (p.Asn249=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2816315	NM_018685.5(ANLN):c.1632T>A (p.Ile544=)	ANLN	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 2813381	NM_018685.5(ANLN):c.481A>G (p.Met161Val)	ANLN (M161V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2812973	NM_018685.5(ANLN):c.1960C>T (p.Pro654Ser)	ANLN (P616S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2803566	NM_018685.5(ANLN):c.769G>A (p.Ala257Thr)	ANLN (A257T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2798339	NM_018685.5(ANLN):c.3024T>G (p.Val1008=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2787855	NM_018685.5(ANLN):c.3269A>G (p.Asp1090Gly)	ANLN (D1052G +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2785409	NM_018685.5(ANLN):c.553_555delinsCAG (p.Arg185Gln)	ANLN (R185Q)	Indel (missense variant)	not provided	GUncertain significance
Select item 2767633	NM_018685.5(ANLN):c.2652+19C>G	ANLN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2763890	NM_018685.5(ANLN):c.1746G>C (p.Lys582Asn)	ANLN (K544N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2762209	NM_018685.5(ANLN):c.1559T>C (p.Leu520Ser)	ANLN (L520S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2762115	NM_018685.5(ANLN):c.1288-6G>T	ANLN	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2761893	NM_018685.5(ANLN):c.3108T>C (p.Asn1036=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2761731	NM_018685.5(ANLN):c.434G>C (p.Arg145Pro)	ANLN (R145P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2759717	NM_018685.5(ANLN):c.24G>A (p.Leu8=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2759235	NM_018685.5(ANLN):c.3079-12_3079-11del	ANLN	Deletion (intron variant)	not provided	GLikely benign
Select item 2755639	NM_018685.5(ANLN):c.2799T>A (p.Ala933=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2744621	NM_018685.5(ANLN):c.18+15G>T	ANLN, MATCAP2 (R6S)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2742774	NM_018685.5(ANLN):c.2653-20T>G	ANLN	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2728323	NM_018685.5(ANLN):c.2329T>C (p.Leu777=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2725970	NM_018685.5(ANLN):c.1396-3C>T	ANLN	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2715693	NM_018685.5(ANLN):c.116G>A (p.Arg39Gln)	ANLN (R39Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2715587	NM_018685.5(ANLN):c.374G>C (p.Gly125Ala)	ANLN (G125A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2711369	NM_018685.5(ANLN):c.3252-6C>T	ANLN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2704314	NM_018685.5(ANLN):c.3237A>G (p.Thr1079=)	ANLN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2663519	NM_018685.5(ANLN):c.2300-107G>A	ANLN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2662490	NM_018685.4(ANLN):c.-201G>T	ANLN, MATCAP2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2662368	NM_018685.5(ANLN):c.2971-72C>T	ANLN	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2630231	NM_018685.5(ANLN):c.1978G>A (p.Asp660Asn)	ANLN (D622N +2 more)	Single nucleotide variant (missense variant)	ANLN-related disorder	GUncertain significance
Select item 2617589	NM_018685.5(ANLN):c.934C>A (p.Gln312Lys)	ANLN (Q312K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2613010	NM_018685.5(ANLN):c.1388C>A (p.Thr463Asn)	ANLN (T463N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2611403	NM_018685.5(ANLN):c.2377C>A (p.Pro793Thr)	ANLN (P756T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2585263	NM_018685.5(ANLN):c.28G>A (p.Glu10Lys)	ANLN (E10K)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2569812	NM_018685.5(ANLN):c.1921G>C (p.Glu641Gln)	ANLN (E603Q +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2560101	NM_018685.5(ANLN):c.229G>A (p.Val77Ile)	ANLN (V77I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548838	NM_018685.5(ANLN):c.3201T>A (p.Asp1067Glu)	ANLN (D1067E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535377	NM_018685.5(ANLN):c.641A>G (p.Asp214Gly)	ANLN (D214G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531160	NM_018685.5(ANLN):c.830C>T (p.Ala277Val)	ANLN (A277V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489311	NM_018685.5(ANLN):c.2794A>C (p.Ser932Arg)	ANLN (S894R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485608	NM_018685.5(ANLN):c.2482G>A (p.Ala828Thr)	ANLN (A791T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484806	NM_018685.5(ANLN):c.2887C>A (p.Pro963Thr)	ANLN (P925T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481842	NM_018685.5(ANLN):c.257A>C (p.Gln86Pro)	ANLN (Q86P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476604	NM_018685.5(ANLN):c.2226C>G (p.Asn742Lys)	ANLN (N704K +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2473867	NM_018685.5(ANLN):c.1004A>C (p.Lys335Thr)	ANLN (K335T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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