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NTD Genetics' Variant Classification Catalog

Please enter the official gene symbol and click Search to see all the variants that have been seen and analyzed by NTD Genetics for that gene.
NTD Genetics classification definitions may be reviewed here.
You may submit a question regarding a variant by clicking the appropriate button on the returned data table.
You may prompt a review of a variant of unknown signifigance (VOUS) reviewed greater than six months ago by clicking the appropriate button on the returned data table.
If a reported variant has changed classification, you may request an amended report by clicking here.
OrderGeneExonNucleotide ChangeProtein ChangeAlias ListingClassificationLast Reviewed  
1SMARCB1Ex3NM_003073.3:c.267C>Tp.Thr89= | p.T89=LRG_520t1:c.267C>T, NM_001007468.1:c.240C>T, NM_003073.3:c.267C>T, XM_005261718.1:c.240C>TLikely benign03/12/2018 
3SMARCB1Ex4NM_003073.3:c.444C>Tp.Ser148= | p.S148=LRG_520t1:c.444C>T, NM_001007468.1:c.417C>T, NM_003073.3:c.444C>T, XM_005261718.1:c.417C>TVOUS01/16/2017
4SMARCB1Ex5NM_003073.3:c.512A>Gp.His171Arg | p.H171RNM_001007468.1:c.485A>G, NM_003073.3:c.512A>G, XM_005261718.1:c.539A>GVOUS08/20/2015
5SMARCB1Ex5NM_003073.3:c.585C>Tp.Ile195= | p.I195=NM_001007468.1:c.558C>T, NM_003073.3:c.585C>T, XM_005261718.1:c.612C>TVOUS03/31/2015
6SMARCB1Ex5NM_003073.3:c.606C>Tp.Asp202= | p.D202=NM_001007468.1:c.579C>T, NM_003073.3:c.606C>TLikely benign04/03/2014 
7SMARCB1Ex7NM_003073.3:c.888G>Tp.Lys296Asn | p.K296NNM_001007468.1:c.861G>T, NM_003073.3:c.888G>T, XM_005261718.1:c.915G>TVOUS03/04/2015
8SMARCB1Ex8NM_003073.3:c.1033G>Tp.Asp345Tyr | p.D345YLRG_520t1:c.1033G>T, NM_001002862.2:c.*3251C>A, NM_001007468.1:c.1006G>T, NM_001135751.1:c.*1209C>A, NM_003073.3:c.1033G>T, NM_198440.3:c.*3442C>A, XM_005261718.1:c.1060G>T, XM_005261820.1:c.*3251C>A, XM_005261821.1:c.*3251C>A, XM_005261822.1:c.*3291C>A, XM_005261823.1:c.*1279C>A, XM_005261824.1:c.*3251C>AVOUS01/19/2021
9SMARCB1Ex9NM_003073.3:c.1131T>Cp.Arg377= | p.R377=NM_001002862.2:c.*2716A>G, NM_001007468.1:c.1104T>C, NM_001135751.1:c.*674A>G, NM_003073.3:c.1131T>C, NM_198440.3:c.*2907A>G, XM_005261718.1:c.1158T>C, XM_005261820.1:c.*2716A>G, XM_005261821.1:c.*2716A>G, XM_005261822.1:c.*2756A>G, XM_005261823.1:c.*744A>G, XM_005261824.1:c.*2716A>GLikely benign07/27/2015 

* Review is pending
** Variant has not been reviewed since the launch of this product (6/15/2012)

URL Parameter Syntax

EmVClass may be automatically searched using the argument [approved_symbol] such as in the example link for the gene CFTR: https://www.egl-eurofins.com/emvclass/emvclass.php?approved_symbol=CFTR


EmVClass data for all genes and variants that have been seen and analyzed by NTD Genetics may be downloaded as a CSV plain text file which is designated to be updated quarterly. Data is subject to change and format is subject to modification.



The interpretation of nucleotide changes is based on our current understanding of the variant at the time it was observed in a clinical case. Interpretations may not be current. Some data may not be represented. These interpretations may change over time as more information about the genes becomes available. The data presented here are not intended for clinical use outside of the context of an official NTD Genetics clinical report and should be approached with caution. Only variants identified at NTD Genetics are listed in the EmVClass. If you intend to use NTD Genetics' classification for publication purposes please contact the laboratory for permission.