ClinVar for Gene (Select 9149) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3358759	NM_004714.3(DYRK1B):c.1556G>A (p.Gly519Asp)	DYRK1B (G479D +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3358716	NM_004714.3(DYRK1B):c.1229G>A (p.Arg410His)	DYRK1B (R370H +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3358700	NM_004714.3(DYRK1B):c.349A>G (p.Ile117Val)	DYRK1B (I117V)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3358618	NM_004714.3(DYRK1B):c.1153G>A (p.Gly385Arg)	DYRK1B (G385R)	Single nucleotide variant (missense variant +1 more)	DYRK1B-related disorder	GUncertain significance
Select item 3358594	NM_004714.3(DYRK1B):c.1526C>T (p.Pro509Leu)	DYRK1B (P469L +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3358433	NM_004714.3(DYRK1B):c.209G>A (p.Arg70Gln)	DYRK1B (R70Q)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3358396	NM_004714.3(DYRK1B):c.86T>A (p.Leu29Gln)	DYRK1B (L29Q)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3358379	NM_004714.3(DYRK1B):c.1380T>C (p.Ser460=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3358348	NM_004714.3(DYRK1B):c.1613C>G (p.Thr538Ser)	DYRK1B (T498S +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3358328	NM_004714.3(DYRK1B):c.999G>A (p.Pro333=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3358302	NM_004714.3(DYRK1B):c.1731A>G (p.Pro577=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3358288	NM_004714.3(DYRK1B):c.*9C>T	DYRK1B	Single nucleotide variant (3 prime UTR variant)	DYRK1B-related disorder	GLikely benign
Select item 3358231	NM_004714.3(DYRK1B):c.1438A>G (p.Asn480Asp)	DYRK1B (N440D +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3358039	NM_004714.3(DYRK1B):c.1753dup (p.Gln585fs)	DYRK1B (Q545fs +2 more)	Duplication (frameshift variant)	DYRK1B-related disorder	GUncertain significance
Select item 3357777	NM_004714.3(DYRK1B):c.475C>T (p.Leu159=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3357700	NM_004714.3(DYRK1B):c.1586C>A (p.Pro529His)	DYRK1B (P489H +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3357362	NM_004714.3(DYRK1B):c.515A>G (p.Tyr172Cys)	DYRK1B (Y172C)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3357359	NM_004714.3(DYRK1B):c.1328C>T (p.Pro443Leu)	DYRK1B (P403L +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3357254	NM_004714.3(DYRK1B):c.957C>T (p.Val319=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3357219	NM_004714.3(DYRK1B):c.1599G>C (p.Ser533=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3357151	NM_004714.3(DYRK1B):c.1296C>A (p.Arg432=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3357066	NM_004714.3(DYRK1B):c.1563G>A (p.Val521=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3356976	NM_004714.3(DYRK1B):c.253AAG[1] (p.Lys86del)	DYRK1B (K86del)	Microsatellite (inframe_deletion)	DYRK1B-related disorder	GUncertain significance
Select item 3356807	NM_004714.3(DYRK1B):c.1652G>A (p.Arg551His)	DYRK1B (R511H +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3356617	NM_004714.3(DYRK1B):c.1309G>A (p.Glu437Lys)	DYRK1B (E397K +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3356556	NM_004714.3(DYRK1B):c.1670C>T (p.Ser557Leu)	DYRK1B (S517L +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3356428	NM_004714.3(DYRK1B):c.1129G>A (p.Glu377Lys)	DYRK1B (E377K)	Single nucleotide variant (missense variant +1 more)	DYRK1B-related disorder	GUncertain significance
Select item 3356390	NM_004714.3(DYRK1B):c.1810C>G (p.Pro604Ala)	DYRK1B (P564A +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3356374	NM_004714.3(DYRK1B):c.489C>T (p.Asn163=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3356234	NM_004714.3(DYRK1B):c.760G>A (p.Ala254Thr)	DYRK1B (A254T)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3356036	NM_004714.3(DYRK1B):c.21T>C (p.His7=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3355763	NM_004714.3(DYRK1B):c.521-4G>T	DYRK1B	Single nucleotide variant (intron variant)	DYRK1B-related disorder	GLikely benign
Select item 3355465	NM_004714.3(DYRK1B):c.954+10C>T	DYRK1B	Single nucleotide variant (intron variant)	DYRK1B-related disorder	GLikely benign
Select item 3355256	NM_004714.3(DYRK1B):c.1742C>T (p.Ala581Val)	DYRK1B (A541V +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3355202	NM_004714.3(DYRK1B):c.1556G>T (p.Gly519Val)	DYRK1B (G479V +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3355164	NM_004714.3(DYRK1B):c.606C>A (p.Arg202=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3355142	NM_004714.3(DYRK1B):c.1316C>G (p.Thr439Ser)	DYRK1B (T399S +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3354318	NM_004714.3(DYRK1B):c.372+10A>T	DYRK1B	Single nucleotide variant (intron variant)	DYRK1B-related disorder	GLikely benign
Select item 3354245	NM_004714.3(DYRK1B):c.927A>C (p.Gly309=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3354130	NM_004714.3(DYRK1B):c.1824C>T (p.Asp608=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3354027	NM_004714.3(DYRK1B):c.1362C>T (p.Pro454=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3353924	NM_004714.3(DYRK1B):c.1352C>T (p.Ser451Leu)	DYRK1B (S411L +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3353913	NM_004714.3(DYRK1B):c.236C>T (p.Ser79Leu)	DYRK1B (S79L)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3353762	NM_004714.3(DYRK1B):c.1583C>A (p.Ala528Asp)	DYRK1B (A488D +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3353731	NM_004714.3(DYRK1B):c.1272G>A (p.Gly424=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3353702	NM_004714.3(DYRK1B):c.1149G>A (p.Thr383=)	DYRK1B	Single nucleotide variant (synonymous variant +1 more)	DYRK1B-related disorder	GLikely benign
Select item 3353645	NM_004714.3(DYRK1B):c.1323G>A (p.Thr441=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3353411	NM_004714.3(DYRK1B):c.588C>T (p.Asn196=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3353181	NM_004714.3(DYRK1B):c.556C>T (p.Leu186=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3353112	NM_004714.3(DYRK1B):c.526C>A (p.Leu176Met)	DYRK1B (L176M)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3353058	NM_004714.3(DYRK1B):c.63G>A (p.Gln21=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GUncertain significance
Select item 3352860	NM_004714.3(DYRK1B):c.17G>C (p.Gly6Ala)	DYRK1B (G6A)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3352804	NM_004714.3(DYRK1B):c.1182G>C (p.Pro394=)	DYRK1B	Single nucleotide variant (synonymous variant +1 more)	DYRK1B-related disorder	GLikely benign
Select item 3352794	NM_004714.3(DYRK1B):c.63+6C>T	DYRK1B	Single nucleotide variant (intron variant)	DYRK1B-related disorder	GLikely benign
Select item 3352675	NM_004714.3(DYRK1B):c.630G>A (p.Ser210=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3352601	NM_004714.3(DYRK1B):c.501G>A (p.Thr167=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3352545	NM_004714.3(DYRK1B):c.1812G>A (p.Pro604=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3352476	NM_004714.3(DYRK1B):c.282C>T (p.Asp94=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3352444	NM_004714.3(DYRK1B):c.80G>A (p.Arg27Gln)	DYRK1B (R27Q)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3352364	NM_004714.3(DYRK1B):c.1678C>T (p.Pro560Ser)	DYRK1B (P520S +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3352318	NM_004714.3(DYRK1B):c.1738C>T (p.Pro580Ser)	DYRK1B (P540S +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3352227	NM_004714.3(DYRK1B):c.1715C>T (p.Pro572Leu)	DYRK1B (P532L +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3352223	NM_004714.3(DYRK1B):c.1111G>C (p.Gly371Arg)	DYRK1B (G371R)	Single nucleotide variant (missense variant +1 more)	DYRK1B-related disorder	GUncertain significance
Select item 3352100	NM_004714.3(DYRK1B):c.1761G>A (p.Pro587=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3351983	NM_004714.3(DYRK1B):c.1659A>G (p.Pro553=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3351894	NM_004714.3(DYRK1B):c.1080G>A (p.Thr360=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3351778	NM_004714.3(DYRK1B):c.253A>G (p.Lys85Glu)	DYRK1B (K85E)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3351620	NM_004714.3(DYRK1B):c.305G>A (p.Arg102His)	DYRK1B (R102H)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3351439	NM_004714.3(DYRK1B):c.195G>A (p.Ala65=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3351049	NM_004714.3(DYRK1B):c.1031G>A (p.Arg344His)	DYRK1B (R344H)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3350996	NM_004714.3(DYRK1B):c.924C>T (p.Thr308=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3350897	NM_004714.3(DYRK1B):c.1651C>T (p.Arg551Cys)	DYRK1B (R511C +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3350834	NM_004714.3(DYRK1B):c.548G>A (p.Arg183Gln)	DYRK1B (R183Q)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3350778	NM_004714.3(DYRK1B):c.1158C>T (p.Pro386=)	DYRK1B	Single nucleotide variant (synonymous variant +1 more)	DYRK1B-related disorder	GLikely benign
Select item 3350694	NM_004714.3(DYRK1B):c.63+5G>A	DYRK1B	Single nucleotide variant (intron variant)	DYRK1B-related disorder	GLikely benign
Select item 3350656	NM_004714.3(DYRK1B):c.1675C>T (p.Pro559Ser)	DYRK1B (P519S +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3350594	NM_004714.3(DYRK1B):c.1743G>A (p.Ala581=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3350536	NM_004714.3(DYRK1B):c.1479T>A (p.Pro493=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3350522	NM_004714.3(DYRK1B):c.137G>A (p.Arg46His)	DYRK1B (R46H)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3350467	NM_004714.3(DYRK1B):c.408T>C (p.Leu136=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3350340	NM_004714.3(DYRK1B):c.1690A>T (p.Met564Leu)	DYRK1B (M524L +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3350253	NM_004714.3(DYRK1B):c.1633del (p.Gln545fs)	DYRK1B (Q505fs +2 more)	Deletion (frameshift variant)	DYRK1B-related disorder	GUncertain significance
Select item 3349992	NM_004714.3(DYRK1B):c.535C>A (p.His179Asn)	DYRK1B (H179N)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3349754	NM_004714.3(DYRK1B):c.1860T>C (p.Gly620=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3349681	NM_004714.3(DYRK1B):c.1734T>C (p.Pro578=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3349515	NM_004714.3(DYRK1B):c.875T>G (p.Leu292Arg)	DYRK1B (L292R)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3349472	NM_004714.3(DYRK1B):c.807+7G>A	DYRK1B	Single nucleotide variant (intron variant)	DYRK1B-related disorder	GLikely benign
Select item 3349400	NM_004714.3(DYRK1B):c.955-10C>T	DYRK1B	Single nucleotide variant (intron variant)	DYRK1B-related disorder	GLikely benign
Select item 3348966	NM_004714.3(DYRK1B):c.359G>T (p.Gly120Val)	DYRK1B (G120V)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3348746	NM_004714.3(DYRK1B):c.1883G>A (p.Ser628Asn)	DYRK1B (S588N +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3348240	NM_004714.3(DYRK1B):c.1769C>T (p.Ser590Leu)	DYRK1B (S550L +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3347973	NM_004714.3(DYRK1B):c.363C>G (p.Ser121=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3347870	NM_004714.3(DYRK1B):c.1697T>C (p.Val566Ala)	DYRK1B (V526A +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3347378	NM_004714.3(DYRK1B):c.1518+9G>A	DYRK1B	Single nucleotide variant (intron variant)	DYRK1B-related disorder	GLikely benign
Select item 3347199	NM_004714.3(DYRK1B):c.477G>T (p.Leu159=)	DYRK1B	Single nucleotide variant (synonymous variant)	DYRK1B-related disorder	GLikely benign
Select item 3346795	NM_004714.3(DYRK1B):c.1411+9C>T	DYRK1B	Single nucleotide variant (intron variant)	DYRK1B-related disorder	GLikely benign
Select item 3346695	NM_004714.3(DYRK1B):c.971G>T (p.Arg324Leu)	DYRK1B (R324L)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3346671	NM_004714.3(DYRK1B):c.1726T>C (p.Ser576Pro)	DYRK1B (S536P +2 more)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance
Select item 3346242	NM_004714.3(DYRK1B):c.1095+10C>T	DYRK1B	Single nucleotide variant (intron variant)	DYRK1B-related disorder	GLikely benign
Select item 3346188	NM_004714.3(DYRK1B):c.991A>G (p.Ile331Val)	DYRK1B (I331V)	Single nucleotide variant (missense variant)	DYRK1B-related disorder	GUncertain significance

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