ClinVar for Gene (Select 22859) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3344024	NM_014921.5(ADGRL1):c.2296T>C (p.Ser766Pro)	ADGRL1, ADGRL1-AS1 (S766P +1 more)	Single nucleotide variant (missense variant)	ADGRL1-related condition	GUncertain significance
Select item 3339124	NM_014921.5(ADGRL1):c.2739G>T (p.Gln913His)	ADGRL1, ADGRL1-AS1 (Q913H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272242	NM_014921.5(ADGRL1):c.1013G>A (p.Arg338His)	ADGRL1, ADGRL1-AS1 (R343H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272231	NM_014921.5(ADGRL1):c.4304A>G (p.Tyr1435Cys)	ADGRL1, ADGRL1-AS1 (Y1435C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272221	NM_014921.5(ADGRL1):c.3033+5G>A	ADGRL1, ADGRL1-AS1	Single nucleotide variant (intron variant)	Inborn genetic diseases	GUncertain significance
Select item 3272212	NM_014921.5(ADGRL1):c.2801C>G (p.Ser934Cys)	ADGRL1, ADGRL1-AS1 (S939C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272203	NM_014921.5(ADGRL1):c.1252A>C (p.Thr418Pro)	ADGRL1, ADGRL1-AS1 (T423P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272194	NM_014921.5(ADGRL1):c.1606G>T (p.Ala536Ser)	ADGRL1, ADGRL1-AS1 (A541S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272186	NM_014921.5(ADGRL1):c.4103G>A (p.Arg1368Gln)	ADGRL1, ADGRL1-AS1 (R1368Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272178	NM_014921.5(ADGRL1):c.3799C>T (p.Arg1267Trp)	ADGRL1, ADGRL1-AS1 (R1272W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272167	NM_014921.5(ADGRL1):c.2320G>A (p.Val774Ile)	ADGRL1, ADGRL1-AS1 (V774I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272158	NM_014921.5(ADGRL1):c.4321C>T (p.Pro1441Ser)	ADGRL1, ADGRL1-AS1 (P1441S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272152	NM_014921.5(ADGRL1):c.2869C>T (p.Arg957Cys)	ADGRL1, ADGRL1-AS1 (R962C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272141	NM_014921.5(ADGRL1):c.2663A>G (p.Asn888Ser)	ADGRL1, ADGRL1-AS1 (N888S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272130	NM_014921.5(ADGRL1):c.2093C>T (p.Pro698Leu)	ADGRL1, ADGRL1-AS1 (P703L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272119	NM_014921.5(ADGRL1):c.1157G>A (p.Arg386His)	ADGRL1, ADGRL1-AS1 (R386H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272109	NM_014921.5(ADGRL1):c.2890G>A (p.Gly964Ser)	ADGRL1, ADGRL1-AS1 (G969S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272100	NM_014921.5(ADGRL1):c.4343C>A (p.Ala1448Glu)	ADGRL1, ADGRL1-AS1 (A1448E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272091	NM_014921.5(ADGRL1):c.946G>A (p.Val316Met)	ADGRL1, ADGRL1-AS1 (V316M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3272081	NM_014921.5(ADGRL1):c.4168C>T (p.Pro1390Ser)	ADGRL1, ADGRL1-AS1 (P1395S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3258089	NM_014921.5(ADGRL1):c.70+2T>C	ADGRL1	Single nucleotide variant (splice donor variant)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GLikely pathogenic
Select item 3258082	NM_014921.5(ADGRL1):c.1367_1383dup (p.Pro462fs)	ADGRL1, ADGRL1-AS1 (P462fs +1 more)	Duplication (frameshift variant)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GLikely pathogenic
Select item 3254635	NM_014921.5(ADGRL1):c.2206G>A (p.Glu736Lys)	ADGRL1, ADGRL1-AS1 (E736K +1 more)	Single nucleotide variant (missense variant)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GUncertain significance
Select item 3251607	NM_014921.5(ADGRL1):c.850C>T (p.Arg284Trp)	ADGRL1, ADGRL1-AS1 (R284W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3236589	NM_014921.5(ADGRL1):c.80G>A (p.Arg27Gln)	ADGRL1 (R27Q)	Single nucleotide variant (missense variant)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GUncertain significance
Select item 3236554	NM_014921.5(ADGRL1):c.3323G>A (p.Arg1108His)	ADGRL1, ADGRL1-AS1 (R1108H +1 more)	Single nucleotide variant (missense variant)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GUncertain significance
Select item 3235844	NM_014921.5(ADGRL1):c.395-3628G>C	ADGRL1, ADGRL1-AS1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3234823	NM_014921.5(ADGRL1):c.3325C>T (p.His1109Tyr)	ADGRL1, ADGRL1-AS1 (H1109Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3234704	NM_014921.5(ADGRL1):c.13G>A (p.Ala5Thr)	ADGRL1 (A5T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3233337	NM_014921.5(ADGRL1):c.393C>A (p.Tyr131Ter)	ADGRL1, ADGRL1-AS1 (Y131*)	Single nucleotide variant (non-coding transcript variant +1 more)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GLikely pathogenic
Select item 3087406	NM_014921.5(ADGRL1):c.982G>A (p.Val328Met)	ADGRL1, ADGRL1-AS1 (V328M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087397	NM_014921.5(ADGRL1):c.7C>T (p.Arg3Cys)	ADGRL1 (R3C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087394	NM_014921.5(ADGRL1):c.79C>T (p.Arg27Trp)	ADGRL1 (R27W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087371	NM_014921.5(ADGRL1):c.677G>A (p.Arg226His)	ADGRL1, ADGRL1-AS1 (R231H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087350	NM_014921.5(ADGRL1):c.614_615insGTTG (p.Val206fs)	ADGRL1, ADGRL1-AS1 (V206fs +1 more)	Insertion (frameshift variant)	Inborn genetic diseases	GPathogenic
Select item 3087344	NM_014921.5(ADGRL1):c.581C>T (p.Ala194Val)	ADGRL1, ADGRL1-AS1 (A194V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087323	NM_014921.5(ADGRL1):c.416T>C (p.Leu139Pro)	ADGRL1, ADGRL1-AS1 (L139P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087308	NM_014921.5(ADGRL1):c.4198C>G (p.Pro1400Ala)	ADGRL1, ADGRL1-AS1 (P1400A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087297	NM_014921.5(ADGRL1):c.4139A>G (p.Tyr1380Cys)	ADGRL1, ADGRL1-AS1 (Y1380C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087266	NM_014921.5(ADGRL1):c.3934G>A (p.Gly1312Arg)	ADGRL1, ADGRL1-AS1 (G1317R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087248	NM_014921.5(ADGRL1):c.3850G>A (p.Val1284Met)	ADGRL1, ADGRL1-AS1 (V1284M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087225	NM_014921.5(ADGRL1):c.3484G>A (p.Ala1162Thr)	ADGRL1, ADGRL1-AS1 (A1162T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087223	NM_014921.5(ADGRL1):c.3467C>T (p.Thr1156Met)	ADGRL1, ADGRL1-AS1 (T1161M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087220	NM_014921.5(ADGRL1):c.3414_3415del (p.Gly1139fs)	ADGRL1, ADGRL1-AS1 (G1139fs +1 more)	Deletion (frameshift variant)	Inborn genetic diseases	GPathogenic
Select item 3087203	NM_014921.5(ADGRL1):c.2923A>G (p.Ile975Val)	ADGRL1, ADGRL1-AS1 (I980V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087201	NM_014921.5(ADGRL1):c.2710C>T (p.Leu904Phe)	ADGRL1, ADGRL1-AS1 (L904F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087198	NM_014921.5(ADGRL1):c.2567C>A (p.Ser856Ter)	ADGRL1, ADGRL1-AS1 (S856* +1 more)	Single nucleotide variant (nonsense)	Inborn genetic diseases	GPathogenic
Select item 3087184	NM_014921.5(ADGRL1):c.2260G>A (p.Ala754Thr)	ADGRL1, ADGRL1-AS1 (A759T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087171	NM_014921.5(ADGRL1):c.2029G>C (p.Glu677Gln)	ADGRL1, ADGRL1-AS1 (E682Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087164	NM_014921.5(ADGRL1):c.1697C>T (p.Ser566Phe)	ADGRL1, ADGRL1-AS1 (S566F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087144	NM_014921.5(ADGRL1):c.1477C>G (p.Leu493Val)	ADGRL1, ADGRL1-AS1 (L493V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087140	NM_014921.5(ADGRL1):c.1445G>A (p.Arg482Gln)	ADGRL1, ADGRL1-AS1 (R487Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3087129	NM_014921.5(ADGRL1):c.1371C>T (p.Pro457=)	ADGRL1, ADGRL1-AS1	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3087120	NM_014921.5(ADGRL1):c.1207T>G (p.Ser403Ala)	ADGRL1, ADGRL1-AS1 (S403A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3068912	NM_014921.5(ADGRL1):c.1910C>G (p.Thr637Arg)	ADGRL1, ADGRL1-AS1 (T637R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3068911	NM_014921.5(ADGRL1):c.3652A>G (p.Ser1218Gly)	ADGRL1, ADGRL1-AS1 (S1218G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3068406	NM_014921.5(ADGRL1):c.2644G>T (p.Gly882Trp)	ADGRL1-AS1, ADGRL1 (G882W +1 more)	Single nucleotide variant (missense variant)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GUncertain significance
Select item 3065132	NM_014921.5(ADGRL1):c.4136T>G (p.Leu1379Arg)	ADGRL1, ADGRL1-AS1 (L1379R +1 more)	Single nucleotide variant (missense variant)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GUncertain significance
Select item 3063758	NM_014921.5(ADGRL1):c.2270_2271del (p.Val757fs)	ADGRL1, ADGRL1-AS1 (V757fs +1 more)	Deletion (frameshift variant)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GPathogenic
Select item 3062393	GRCh37/hg19 19p13.13-13.11(chr19:13970692-18139376)x3	CYP4F8, DCAF15 +109 more	Copy number gain	not specified	GUncertain significance
Select item 3025818	NM_014921.5(ADGRL1):c.2529T>G (p.Arg843=)	ADGRL1, ADGRL1-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2867530	NM_014921.5(ADGRL1):c.608C>G (p.Pro203Arg)	ADGRL1, ADGRL1-AS1 (P208R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2692481	NM_014921.5(ADGRL1):c.3001A>C (p.Ser1001Arg)	ADGRL1, ADGRL1-AS1 (S1001R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2692453	NM_014921.5(ADGRL1):c.4131C>A (p.Asp1377Glu)	ADGRL1, ADGRL1-AS1 (D1377E +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2692339	NM_014921.5(ADGRL1):c.710T>C (p.Ile237Thr)	ADGRL1, ADGRL1-AS1 (I237T +1 more)	Single nucleotide variant (missense variant)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GUncertain significance
Select item 2682363	NM_014921.5(ADGRL1):c.3712C>A (p.Pro1238Thr)	ADGRL1, ADGRL1-AS1 (P1238T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2671964	NM_014921.5(ADGRL1):c.371_372dup (p.Gln125fs)	ADGRL1, ADGRL1-AS1 (Q125fs)	Duplication (non-coding transcript variant +1 more)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GLikely pathogenic
Select item 2664815	NM_014921.5(ADGRL1):c.671G>A (p.Arg224His)	ADGRL1, ADGRL1-AS1 (R224H +1 more)	Single nucleotide variant (missense variant)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GUncertain significance
Select item 2663877	NM_014921.5(ADGRL1):c.3256dup (p.Val1086fs)	ADGRL1, ADGRL1-AS1 (V1086fs +1 more)	Duplication (non-coding transcript variant +1 more)	Developmental delay, behavioral abnormalities, and neuropsychiatric disorders	GPathogenic
Select item 2649419	NM_014921.5(ADGRL1):c.197C>T (p.Thr66Met)	ADGRL1 (T66M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2649418	NM_014921.5(ADGRL1):c.1195+3G>A	ADGRL1, ADGRL1-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2649417	NM_014921.5(ADGRL1):c.1623T>C (p.Ser541=)	ADGRL1, ADGRL1-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2649416	NM_014921.5(ADGRL1):c.1890C>G (p.Ser630=)	ADGRL1, ADGRL1-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2649415	NM_014921.5(ADGRL1):c.3851T>C (p.Val1284Ala)	ADGRL1, ADGRL1-AS1 (V1284A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2627824	NM_014921.5(ADGRL1):c.3427C>T (p.Arg1143Ter)	ADGRL1, ADGRL1-AS1 (R1143* +1 more)	Single nucleotide variant (nonsense)	Neurodevelopmental disorder	GUncertain significance
Select item 2626902	NM_014921.5(ADGRL1):c.400G>C (p.Val134Leu)	ADGRL1, ADGRL1-AS1 (V134L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2613392	NM_014921.5(ADGRL1):c.2435C>T (p.Ser812Leu)	ADGRL1, ADGRL1-AS1 (S817L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2607874	NM_014921.5(ADGRL1):c.3974G>A (p.Arg1325Gln)	ADGRL1, ADGRL1-AS1 (R1330Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2607203	NM_014921.5(ADGRL1):c.428T>G (p.Leu143Arg)	ADGRL1, ADGRL1-AS1 (L143R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2589639	NM_014921.5(ADGRL1):c.1684G>A (p.Ala562Thr)	ADGRL1, ADGRL1-AS1 (A567T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2588912	NM_014921.5(ADGRL1):c.2230G>A (p.Gly744Ser)	ADGRL1, ADGRL1-AS1 (G749S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2582968	NM_014921.5(ADGRL1):c.1432C>T (p.Arg478Ter)	ADGRL1, ADGRL1-AS1 (R478* +1 more)	Single nucleotide variant (nonsense)	not provided	GLikely pathogenic
Select item 2569022	NM_014921.5(ADGRL1):c.2228C>A (p.Ala743Asp)	ADGRL1, ADGRL1-AS1 (A743D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2557842	NM_014921.5(ADGRL1):c.3134C>T (p.Ala1045Val)	ADGRL1, ADGRL1-AS1 (A1050V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2550258	NM_014921.5(ADGRL1):c.2065G>A (p.Glu689Lys)	ADGRL1, ADGRL1-AS1 (E694K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2548760	NM_014921.5(ADGRL1):c.1289G>A (p.Arg430His)	ADGRL1, ADGRL1-AS1 (R435H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2548681	NM_014921.5(ADGRL1):c.614G>A (p.Arg205His)	ADGRL1, ADGRL1-AS1 (R210H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2539191	NM_014921.5(ADGRL1):c.932C>T (p.Ser311Phe)	ADGRL1, ADGRL1-AS1 (S316F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2535097	NM_014921.5(ADGRL1):c.3022T>G (p.Phe1008Val)	ADGRL1, ADGRL1-AS1 (F1013V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2526805	NM_014921.5(ADGRL1):c.1270G>A (p.Ala424Thr)	ADGRL1, ADGRL1-AS1 (A424T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2525390	NM_014921.5(ADGRL1):c.652G>A (p.Val218Ile)	ADGRL1, ADGRL1-AS1 (V218I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2524545	NM_014921.5(ADGRL1):c.3800G>A (p.Arg1267Gln)	ADGRL1, ADGRL1-AS1 (R1272Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2523663	NM_014921.5(ADGRL1):c.3148G>A (p.Ala1050Thr)	ADGRL1, ADGRL1-AS1 (A1050T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2495161	NM_014921.5(ADGRL1):c.758C>T (p.Ser253Leu)	ADGRL1, ADGRL1-AS1 (S253L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488440	NM_014921.5(ADGRL1):c.718G>A (p.Gly240Arg)	ADGRL1, ADGRL1-AS1 (G245R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2484295	NM_014921.5(ADGRL1):c.1189A>G (p.Ser397Gly)	ADGRL1, ADGRL1-AS1 (S397G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2474566	NM_014921.5(ADGRL1):c.4184G>A (p.Ser1395Asn)	ADGRL1, ADGRL1-AS1 (S1400N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2472996	NM_014921.5(ADGRL1):c.22C>G (p.Leu8Val)	ADGRL1 (L8V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2471601	NM_014921.5(ADGRL1):c.1142A>G (p.Asn381Ser)	ADGRL1, ADGRL1-AS1 (N386S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2470494	NM_014921.5(ADGRL1):c.4253A>T (p.Tyr1418Phe)	ADGRL1, ADGRL1-AS1 (Y1423F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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