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Mutation Direct

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Gene: ANK3 & Disease: MRT37, 444 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
1408693	ANK3	c.3604A>G	p.Ile1202Val (p.I1202V)	NM_020987.5 M	SNV	VUS	1 +	2
587453	ANK3	c.4723C>T	p.Arg1575Trp (p.R1575W)	NM_020987.5 M	SNV	VUS	1 +	2
1515430	ANK3	c.7928A>G	p.Asn2643Ser (p.N2643S)	NM_020987.5 M	SNV	VUS	1 +	2
434147	ANK3	c.13106G>A	p.Arg4369Gln (p.R4369Q)	NM_020987.5 M	SNV	LB	1 +	2
434154	ANK3	c.10688A>G	p.Glu3563Gly (p.E3563G)	NM_020987.5 M	SNV	LB	1 +	2
434156	ANK3	c.9997A>T	p.Thr3333Ser (p.T3333S)	NM_020987.5 M	SNV	LB	1 +	2
434188	ANK3	c.6916A>G	p.Lys2306Glu (p.K2306E)	NM_020987.5 M	SNV	VUS	1 +	2
1298482	ANK3	c.10397T>A	p.Val3466Asp (p.V3466D)	NM_020987.5 M	SNV	VUS	1 +	2
1298486	ANK3	c.671A>G	p.Asn224Ser (p.N224S)	NM_020987.5 M	SNV	VUS	1 +	2
1429615	ANK3	c.3728G>A	p.Arg1243His (p.R1243H)	NM_020987.5 M	SNV	VUS	1 +	2
389255	ANK3	c.1882G>A	p.Ala628Thr (p.A628T)	NM_020987.5 M	SNV	VUS	1 +	2
1370441	ANK3	c.4459T>C	p.Ser1487Pro (p.S1487P)	NM_020987.5 M	SNV	VUS	1 +	2
713120	ANK3	c.3984G>A	p.Leu1328= (p.L1328=)	NM_020987.5 M	SNV	LB	1 +	2
434169	ANK3	c.4907G>A	p.Arg1636Lys (p.R1636K)	NM_020987.5 M	SNV	LB	1 +	2
1030746	ANK3	c.2467A>G	p.Met823Val (p.M823V)	NM_020987.5 M	SNV	VUS	1 +	2
1030749	ANK3	c.9965C>T	p.Ser3322Phe (p.S3322F)	NM_020987.5 M	SNV	VUS	1 +	2
729719	ANK3	c.4403G>A	p.Arg1468His (p.R1468H)	NM_020987.5 M	SNV	LB	1 +	2
377485	ANK3	c.9935C>T	p.Ala3312Val (p.A3312V)	NM_020987.5 M	SNV	LB	1 +	2
252732	ANK3	c.2555G>A	p.Arg852His (p.R852H)	NM_020987.5 M	SNV	VUS	1 +	2
930643	ANK3	c.13130C>T	p.Ser4377Leu (p.S4377L)	NM_020987.5 M	SNV	VUS	1 +	2

444 Results, 20 per Page

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