List of variants in gene DSP reported as likely benign by Fulgent Genetics, Fulgent 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: 27

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.1481A>T (p.Tyr494Phe)	rs28763961	0.00618
NM_004415.4(DSP):c.105G>A (p.Gly35=)	rs77445784	0.00587
NM_004415.4(DSP):c.2630+18C>T	rs145963404	0.00475
NM_004415.4(DSP):c.522T>C (p.Cys174=)	rs144781697	0.00124
NM_004415.4(DSP):c.8605A>G (p.Ile2869Val)	rs28763971	0.00077
NM_004415.4(DSP):c.7599T>C (p.Ala2533=)	rs374266378	0.00016
NM_004415.4(DSP):c.6799A>T (p.Thr2267Ser)	rs181378432	0.00011
NM_004415.4(DSP):c.888C>T (p.Tyr296=)	rs149701627	0.00008
NM_004415.4(DSP):c.1155G>A (p.Ala385=)	rs140488069	0.00006
NM_004415.4(DSP):c.4914C>T (p.Asp1638=)	rs750113099	0.00006
NM_004415.4(DSP):c.1983T>C (p.Asn661=)	rs770735715	0.00005
NM_004415.4(DSP):c.1443G>A (p.Glu481=)	rs149126992	0.00004
NM_004415.4(DSP):c.5193C>T (p.Tyr1731=)	rs201663619	0.00002
NM_004415.4(DSP):c.1545G>A (p.Pro515=)	rs747953037	0.00001
NM_004415.4(DSP):c.1860G>A (p.Gln620=)	rs762658467	0.00001
NM_004415.4(DSP):c.3843C>T (p.Gly1281=)	rs757848395	0.00001
NM_004415.4(DSP):c.3864G>A (p.Lys1288=)	rs768166626	0.00001
NM_004415.4(DSP):c.6441C>A (p.Val2147=)	rs762513279	0.00001
NM_004415.4(DSP):c.8277C>T (p.Arg2759=)	rs1248664648	0.00001
NM_004415.4(DSP):c.8508A>G (p.Gly2836=)	rs754074127	0.00001
NM_004415.4(DSP):c.8511T>C (p.Ser2837=)	rs757475874	0.00001
NM_004415.4(DSP):c.939+19G>T	rs777724973	0.00001
NM_004415.4(DSP):c.2091A>T (p.Gly697=)	rs2076304
NM_004415.4(DSP):c.2436+16A>G	rs199555263
NM_004415.4(DSP):c.5116C>T (p.Leu1706=)	rs1759432452
NM_004415.4(DSP):c.6441C>T (p.Val2147=)	rs762513279
NM_004415.4(DSP):c.78G>T (p.Leu26=)	rs71559180

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.