List of variants in gene LOC107982234, WT1 studied for Nephroblastoma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.213G>T (p.Pro71=)	rs2234582	0.31689
NM_024426.6(WT1):c.345C>T (p.Pro115=)	rs1799925	0.15374
NM_024426.6(WT1):c.609C>T (p.Asn203=)	rs2234583	0.13287
NM_024426.6(WT1):c.181C>A (p.Arg61=)	rs2234581	0.00270
NM_024426.6(WT1):c.123G>C (p.Pro41=)	rs555140661	0.00188
NM_024426.6(WT1):c.-31G>T	rs886048234
NM_024426.6(WT1):c.-82A>C	rs886048236
NM_024426.6(WT1):c.-86T>C	rs886048237
NM_024426.6(WT1):c.-90T>C	rs886048238
NM_024426.6(WT1):c.-94G>C	rs886048239
NM_024426.6(WT1):c.136G>T (p.Ala46Ser)	rs886048233
NM_024426.6(WT1):c.247G>T (p.Ala83Ser)	rs886048231
NM_024426.6(WT1):c.285C>T (p.Gly95=)	rs886048230
NM_024426.6(WT1):c.411GCC[5] (p.Pro141dup)	rs760304811

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.