List of variants reported as likely pathogenic for Noonan syndrome by Juno Genomics, Hangzhou Juno Genomics, Inc

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

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.264-13G>A	rs587777176	0.00017
NM_006767.4(LZTR1):c.850C>T (p.Arg284Cys)	rs797045165	0.00001
NM_002834.5(PTPN11):c.1502G>A (p.Arg501Lys)	rs397507543
NM_002834.5(PTPN11):c.167T>C (p.Ile56Thr)	rs1052382672
NM_002834.5(PTPN11):c.329A>C (p.Glu110Ala)	rs397507519
NM_002880.4(RAF1):c.779C>A (p.Thr260Lys)	rs869025501
NM_005633.4(SOS1):c.322G>A (p.Glu108Lys)	rs397517164
NM_006767.4(LZTR1):c.1150-1G>A
NM_006767.4(LZTR1):c.200+1G>T
NM_006767.4(LZTR1):c.855C>A (p.Tyr285Ter)
NM_006912.6(RIT1):c.269T>C (p.Met90Thr)

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.