List of variants in gene RAET1L reported as uncertain significance by Ambry Genetics

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: 26

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_130900.3(RAET1L):c.619C>A (p.Pro207Thr)	rs147812292	0.00058
NM_130900.3(RAET1L):c.433G>A (p.Gly145Arg)	rs369430003	0.00019
NM_130900.3(RAET1L):c.575G>A (p.Gly192Glu)	rs141345751	0.00019
NM_130900.3(RAET1L):c.530A>T (p.Asp177Val)	rs148747435	0.00015
NM_130900.3(RAET1L):c.158A>C (p.Gln53Pro)	rs1164537248	0.00003
NM_130900.3(RAET1L):c.391G>A (p.Ala131Thr)	rs1170971867	0.00001
NM_130900.3(RAET1L):c.113C>A (p.Thr38Asn)	rs137965307
NM_130900.3(RAET1L):c.161G>A (p.Gly54Asp)
NM_130900.3(RAET1L):c.203A>G (p.Asn68Ser)
NM_130900.3(RAET1L):c.284G>C (p.Arg95Thr)
NM_130900.3(RAET1L):c.29T>C (p.Leu10Pro)	rs2483165888
NM_130900.3(RAET1L):c.319G>A (p.Asp107Asn)	rs2483156318
NM_130900.3(RAET1L):c.359C>T (p.Thr120Ile)	rs530963292
NM_130900.3(RAET1L):c.361C>G (p.Leu121Val)	rs1285244129
NM_130900.3(RAET1L):c.400C>T (p.His134Tyr)	rs2483154595
NM_130900.3(RAET1L):c.442T>C (p.Phe148Leu)
NM_130900.3(RAET1L):c.460G>A (p.Glu154Lys)	rs61748299
NM_130900.3(RAET1L):c.499A>C (p.Lys167Gln)
NM_130900.3(RAET1L):c.513G>T (p.Lys171Asn)
NM_130900.3(RAET1L):c.539T>A (p.Met180Lys)	rs147287797
NM_130900.3(RAET1L):c.553A>C (p.Ile185Leu)
NM_130900.3(RAET1L):c.61G>T (p.Gly21Cys)
NM_130900.3(RAET1L):c.671C>T (p.Ala224Val)
NM_130900.3(RAET1L):c.689T>C (p.Ile230Thr)	rs2483152183
NM_130900.3(RAET1L):c.84C>G (p.Asp28Glu)
NM_130900.3(RAET1L):c.87C>A (p.Asp29Glu)

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.