ClinVar for Gene (Select 816) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3373340	NM_001220.5(CAMK2B):c.1987G>T (p.Ala663Ser)	CAMK2B (A446S +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3373193	NM_001220.5(CAMK2B):c.983C>T (p.Thr328Ile)	CAMK2B (T328I)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3371751	NM_001220.5(CAMK2B):c.1618A>G (p.Lys540Glu)	CAMK2B (K323E +6 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3370848	NM_001220.5(CAMK2B):c.475G>A (p.Gly159Ser)	CAMK2B (G159S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3369144	NM_001220.5(CAMK2B):c.275+1G>A	CAMK2B	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 3368851	NM_001220.5(CAMK2B):c.341+5G>C	CAMK2B	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3368384	NM_001220.5(CAMK2B):c.413A>G (p.Lys138Arg)	CAMK2B (K138R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3367634	NM_001220.5(CAMK2B):c.1768+1G>C	CAMK2B	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 3367439	NM_001220.5(CAMK2B):c.430C>A (p.Leu144Met)	CAMK2B (L144M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3365868	NM_001220.5(CAMK2B):c.1862G>A (p.Arg621Gln)	CAMK2B (R404Q +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3363417	NM_001220.5(CAMK2B):c.1801A>C (p.Thr601Pro)	CAMK2B (T384P +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3362132	NM_001220.5(CAMK2B):c.59T>C (p.Ile20Thr)	CAMK2B (I20T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361574	NM_001220.5(CAMK2B):c.1202C>T (p.Thr401Ile)	CAMK2B (T338I +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3361194	NM_001220.5(CAMK2B):c.1167C>A (p.Asp389Glu)	CAMK2B (D364E +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3360442	NM_001220.5(CAMK2B):c.414+5G>C	CAMK2B	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3360295	NM_001220.5(CAMK2B):c.1762G>A (p.Glu588Lys)	CAMK2B (E371K +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3359960	NM_001220.5(CAMK2B):c.481G>A (p.Ala161Thr)	CAMK2B (A161T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3356416	NM_001220.5(CAMK2B):c.1340C>T (p.Ser447Phe)	CAMK2B (S447F)	Single nucleotide variant (missense variant +1 more)	CAMK2B-related disorder	GUncertain significance
Select item 3344387	NM_001220.5(CAMK2B):c.1801_1819dup (p.Val607fs)	CAMK2B (V390fs +7 more)	Duplication (frameshift variant)	CAMK2B-related disorder	GUncertain significance
Select item 3342936	NM_001220.5(CAMK2B):c.66-1G>T	CAMK2B	Single nucleotide variant (splice acceptor variant)	not provided	GUncertain significance
Select item 3340997	NM_001220.5(CAMK2B):c.814dup (p.Val272fs)	CAMK2B (V272fs)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 3339572	NM_001220.5(CAMK2B):c.160+13G>T	CAMK2B	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3339174	NM_001220.5(CAMK2B):c.486C>A (p.Ile162=)	CAMK2B	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3339087	NM_001220.5(CAMK2B):c.1176+10C>T	CAMK2B	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3257390	NM_001220.5(CAMK2B):c.1312G>A (p.Ala438Thr)	CAMK2B (A438T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3253484	NM_001220.5(CAMK2B):c.920C>A (p.Thr307Asn)	CAMK2B (T307N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3253351	NM_001220.5(CAMK2B):c.947-2A>G	CAMK2B	Single nucleotide variant (intron variant +1 more)	not provided	GUncertain significance
Select item 3252732	NM_001220.5(CAMK2B):c.496G>A (p.Gly166Arg)	CAMK2B (G166R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3245902	NC_000007.13:g.(?_43810758)_(45977174_?)del	ADCY1, AEBP1 +31 more	Deletion	not provided	GUncertain significance
Select item 3245869	NC_000007.13:g.(?_44259661)_(44274295_?)dup	CAMK2B	Duplication	not provided	GUncertain significance
Select item 3245868	NC_000007.13:g.(?_44268375)_(44365020_?)dup	CAMK2B	Duplication	not provided	GUncertain significance
Select item 3233718	NM_001220.5(CAMK2B):c.1266C>T (p.Gly422=)	CAMK2B	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3055047	NM_001220.5(CAMK2B):c.859_867del (p.Thr287_Glu289del)	CAMK2B	Deletion	CAMK2B-related disorder	GUncertain significance
Select item 3026851	NM_001220.5(CAMK2B):c.1421C>T (p.Pro474Leu)	CAMK2B (P474L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3026684	NM_001220.5(CAMK2B):c.1845C>T (p.Ala615=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3018499	NM_001220.5(CAMK2B):c.1212T>C (p.Asp404=)	CAMK2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3012223	NM_001220.5(CAMK2B):c.618C>A (p.Ile206=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3012099	NM_001220.5(CAMK2B):c.657G>A (p.Gln219=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3009481	NM_001220.5(CAMK2B):c.946+3G>A	CAMK2B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3003400	NM_001220.5(CAMK2B):c.1582C>T (p.Pro528Ser)	CAMK2B (P528S)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 3002535	NM_001220.5(CAMK2B):c.1582C>G (p.Pro528Ala)	CAMK2B (P528A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2999376	NM_001220.5(CAMK2B):c.1743C>T (p.Asp581=)	CAMK2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2999096	NM_001220.5(CAMK2B):c.1459T>G (p.Ser487Ala)	CAMK2B (S487A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2998895	NM_001220.5(CAMK2B):c.1531G>A (p.Gly511Ser)	CAMK2B (G511S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2994296	NM_001220.5(CAMK2B):c.1947G>A (p.Lys649=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2992201	NM_001220.5(CAMK2B):c.1330C>T (p.Pro444Ser)	CAMK2B (P444S)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2991911	NM_001220.5(CAMK2B):c.624C>G (p.Leu208=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2991853	NM_001220.5(CAMK2B):c.507G>A (p.Gln169=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2991368	NM_001220.5(CAMK2B):c.1290G>T (p.Gly430=)	CAMK2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2991065	NM_001220.5(CAMK2B):c.1673+18_1673+19insC	CAMK2B	Insertion (intron variant)	not provided	GLikely benign
Select item 2990119	NM_001220.5(CAMK2B):c.1597+13T>C	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2989819	NM_001220.5(CAMK2B):c.1131+12C>T	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2989028	NM_001220.5(CAMK2B):c.1457T>C (p.Leu486Pro)	CAMK2B (L486P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2988887	NM_001220.5(CAMK2B):c.1425G>A (p.Pro475=)	CAMK2B	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 2988623	NM_001220.5(CAMK2B):c.1672G>T (p.Ala558Ser)	CAMK2B (A395S +6 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2988197	NM_001220.5(CAMK2B):c.1639G>A (p.Glu547Lys)	CAMK2B (E384K +6 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2988134	NM_001220.5(CAMK2B):c.396C>G (p.Val132=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2985169	NM_001220.5(CAMK2B):c.1673+18_1673+19insT	CAMK2B	Insertion (intron variant)	not provided	GLikely benign
Select item 2984293	NM_001220.5(CAMK2B):c.1543G>C (p.Val515Leu)	CAMK2B (V515L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2984002	NM_001220.5(CAMK2B):c.1673+20G>A	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2983132	NM_001220.5(CAMK2B):c.276-19C>T	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2982128	NM_001220.5(CAMK2B):c.1461C>T (p.Ser487=)	CAMK2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2981082	NM_001220.5(CAMK2B):c.1420C>A (p.Pro474Thr)	CAMK2B (P474T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2979453	NM_001220.5(CAMK2B):c.624C>T (p.Leu208=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2977881	NM_001220.5(CAMK2B):c.1653C>T (p.Asn551=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2977480	NM_001220.5(CAMK2B):c.540C>T (p.Tyr180=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2976508	NM_001220.5(CAMK2B):c.1541C>A (p.Pro514Gln)	CAMK2B (P514Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2968060	NM_001220.5(CAMK2B):c.1469-15T>A	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2967778	NM_001220.5(CAMK2B):c.1340C>G (p.Ser447Cys)	CAMK2B (S447C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2967353	NM_001220.5(CAMK2B):c.831G>A (p.Thr277=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2966505	NM_001220.5(CAMK2B):c.1673+18G>C	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2966080	NM_001220.5(CAMK2B):c.904-14G>A	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2965928	NM_001220.5(CAMK2B):c.1957G>A (p.Val653Met)	CAMK2B (V479M +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2959202	NM_001220.5(CAMK2B):c.1021+14G>A	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2957725	NM_001220.5(CAMK2B):c.1469-12G>C	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2957105	NM_001220.5(CAMK2B):c.224G>A (p.Arg75His)	CAMK2B (R75H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2955799	NM_001220.5(CAMK2B):c.1021+20C>T	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2918096	NM_001220.5(CAMK2B):c.1934G>A (p.Arg645His)	CAMK2B (R497H +7 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 2914490	NM_001220.5(CAMK2B):c.1112C>T (p.Thr371Met)	CAMK2B (T347M +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2907470	NM_001220.5(CAMK2B):c.341+10G>A	CAMK2B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2894614	NM_001220.5(CAMK2B):c.1691G>A (p.Gly564Glu)	CAMK2B (G347E +6 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2894278	NM_001220.5(CAMK2B):c.1168G>A (p.Gly390Arg)	CAMK2B (G366R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2889466	NM_001220.5(CAMK2B):c.1673C>T (p.Ala558Val)	CAMK2B (A434V +6 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2882977	NM_001220.5(CAMK2B):c.327C>T (p.Ser109=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2882468	NM_001220.5(CAMK2B):c.415-5T>C	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2881338	NM_001220.5(CAMK2B):c.1769-15G>C	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2881169	NM_001220.5(CAMK2B):c.1522G>C (p.Glu508Gln)	CAMK2B (E508Q)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2880918	NM_001220.5(CAMK2B):c.486C>T (p.Ile162=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2878938	NM_001220.5(CAMK2B):c.1305A>G (p.Pro435=)	CAMK2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2878183	NM_001220.5(CAMK2B):c.1577C>G (p.Pro526Arg)	CAMK2B (P526R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2876593	NM_001220.5(CAMK2B):c.1257G>A (p.Val419=)	CAMK2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2876221	NM_001220.5(CAMK2B):c.1512A>C (p.Ser504=)	CAMK2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2875437	NM_001220.5(CAMK2B):c.1469-17C>T	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2875431	NM_001220.5(CAMK2B):c.1499T>C (p.Val500Ala)	CAMK2B (V500A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2873382	NM_001220.5(CAMK2B):c.960C>T (p.Thr320=)	CAMK2B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2869140	NM_001220.5(CAMK2B):c.1872G>A (p.Gln624=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2868093	NM_001220.5(CAMK2B):c.1022-15C>T	CAMK2B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2868007	NM_001220.5(CAMK2B):c.1241A>G (p.Asp414Gly)	CAMK2B (D414G)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2867197	NM_001220.5(CAMK2B):c.1560C>A (p.Cys520Ter)	CAMK2B (C520*)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 2866315	NM_001220.5(CAMK2B):c.93T>C (p.Cys31=)	CAMK2B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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