List of variants in gene PTPN11 reported as benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 31

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002834.5(PTPN11):c.14+25G>C	rs7972574	0.05545
NM_002834.5(PTPN11):c.854-21C>T	rs41279090	0.05308
NM_002834.5(PTPN11):c.1093-9C>A	rs12301915	0.04151
NM_002834.5(PTPN11):c.255C>T (p.His85=)	rs61736914	0.02271
NM_002834.5(PTPN11):c.525+12G>C	rs41304351	0.01035
NM_002834.5(PTPN11):c.854-30T>C	rs144391508	0.00909
NM_002834.5(PTPN11):c.854-32A>C	rs187389813	0.00867
NM_002834.5(PTPN11):c.332+17T>G	rs115658366	0.00257
NM_002834.5(PTPN11):c.526-17T>C	rs375184329	0.00096
NM_002834.5(PTPN11):c.526-8C>A	rs184804143	0.00064
NM_002834.5(PTPN11):c.1448-38G>C	rs186280715	0.00060
NM_002834.5(PTPN11):c.1658C>T (p.Thr553Met)	rs148176616	0.00048
NM_002834.5(PTPN11):c.1379+20C>T	rs184743462	0.00047
NM_002834.3(PTPN11):c.*13A>G	rs201957261	0.00027
NM_002834.5(PTPN11):c.333-3T>C	rs146749153	0.00026
NM_002834.5(PTPN11):c.925A>G (p.Ile309Val)	rs201787206	0.00026
NM_002834.5(PTPN11):c.-45T>G	rs587781131	0.00018
NM_002834.5(PTPN11):c.1746C>T (p.Asn582=)	rs397516800	0.00013
NM_002834.5(PTPN11):c.*50C>T	rs730880328	0.00012
NM_002834.5(PTPN11):c.558G>T (p.Arg186=)	rs200920312	0.00011
NM_002834.5(PTPN11):c.486C>T (p.Asp162=)	rs397507522	0.00009
NM_002834.5(PTPN11):c.1404G>C (p.Thr468=)	rs587781130	0.00003
NM_002834.5(PTPN11):c.879C>T (p.His293=)	rs117730996	0.00003
NM_002834.5(PTPN11):c.934-12C>T	rs730880990	0.00002
NM_002834.5(PTPN11):c.1620C>T (p.His540=)	rs587781132	0.00001
NM_002834.5(PTPN11):c.1650G>A (p.Ala550=)	rs374896287	0.00001
NM_002834.5(PTPN11):c.951G>A (p.Lys317=)	rs576405446	0.00001
NM_002834.5(PTPN11):c.1052G>A (p.Arg351Gln)	rs397507534
NM_002834.5(PTPN11):c.1221A>G (p.Gly407=)	rs532529560
NM_002834.5(PTPN11):c.1448-15_1448-13del	rs775920290
NM_002834.5(PTPN11):c.333-19del	rs766492276

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.