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Gene: WT1 & Disease: Chromosome 11p Deletion, 10141 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
3500	WT1	c.1447+4C>T	--	NM_024426.6 M	SNV	P	7 +	31
	WT1	c.1273+4C>T	--	NM_001407050.1	SNV	P	7 +	31
	WT1	c.1315+13C>T	--	NM_001407047.1	SNV	P	7 +	31
	WT1	c.1306+4C>T	--	NM_001407048.1	SNV	P	7 +	31
	WT1	c.1303+698C>T	--	NM_001407049.1	SNV	P	7 +	31
	WT1	c.1387+13C>T	--	NM_000378.6	SNV	P	7 +	31
	WT1	c.1396+4C>T	--	NM_001407045.1	SNV	P	7 +	31
	WT1	c.1432+13C>T	--	NM_001407044.1	SNV	P	7 +	31
	WT1	c.1354+698C>T	--	NM_001407046.1	SNV	P	7 +	31
	WT1	c.1438+13C>T	--	NM_024424.5	SNV	P	7 +	31
	WT1	c.685+4C>T	--	NM_001407051.1	SNV	P	7 +	31
	WT1	c.745+4C>T	--	NM_001198552.2	SNV	P	7 +	31
	WT1	c.787+13C>T	--	NM_001198551.2	SNV	P	7 +	31
	WT1	c.259+4C>T	--	NM_001367854.1	SNV	P	7 +	31
3487	WT1	c.1399C>T	p.Arg467Trp (p.R467W)	NM_024426.6 M	SNV	P	10 +	30
	WT1	c.1348C>T	p.Arg450Trp (p.R450W)	NM_000378.6	SNV	P	10 +	30
	WT1	c.748C>T	p.Arg250Trp (p.R250W)	NM_001198551.2	SNV	P	10 +	30
	WT1	c.697C>T	p.Arg233Trp (p.R233W)	NM_001198552.2	SNV	P	10 +	30
	WT1	c.211C>T	p.Arg71Trp (p.R71W)	NM_001367854.1	SNV	P	10 +	30
	WT1	c.1393C>T	p.Arg465Trp (p.R465W)	NM_001407044.1	SNV	P	10 +	30

10141 Results, 20 per Page

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