List of variants in gene DSP reported as benign 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: 34

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.741= (p.Ala247=)	rs2806234	0.99917
NM_004415.4(DSP):c.2091A>G (p.Gly697=)	rs2076304	0.76849
NM_004415.4(DSP):c.2631G>A (p.Arg877=)	rs1016835	0.74603
NM_004415.4(DSP):c.8472G>C (p.Gly2824=)	rs2744380	0.68624
NM_004415.4(DSP):c.7122C>T (p.Thr2374=)	rs2076300	0.28306
NM_004415.4(DSP):c.2862C>T (p.Cys954=)	rs2064217	0.27166
NM_004415.4(DSP):c.5213G>A (p.Arg1738Gln)	rs6929069	0.19612
NM_004415.4(DSP):c.1dup (p.Met1fs)	rs17133512	0.17362
NM_004415.4(DSP):c.4535A>G (p.Tyr1512Cys)	rs2076299	0.13777
NM_004415.4(DSP):c.126T>C (p.Tyr42=)	rs36087964	0.06956
NM_004415.4(DSP):c.4578C>A (p.Asn1526Lys)	rs28763966	0.04717
NM_004415.4(DSP):c.8175C>A (p.Arg2725=)	rs11558731	0.04375
NM_004415.4(DSP):c.913A>T (p.Ile305Phe)	rs17604693	0.02655
NM_004415.4(DSP):c.4773G>A (p.Arg1591=)	rs28763968	0.01341
NM_004415.4(DSP):c.2815G>A (p.Gly939Ser)	rs80325569	0.01244
NM_004415.4(DSP):c.3963G>A (p.Gln1321=)	rs61731476	0.01161
NM_004415.4(DSP):c.3510G>A (p.Glu1170=)	rs28763964	0.01023
NM_004415.4(DSP):c.6390T>C (p.Ala2130=)	rs28763969	0.00940
NM_004415.4(DSP):c.4609C>T (p.Arg1537Cys)	rs28763967	0.00925
NM_004415.4(DSP):c.5498A>T (p.Glu1833Val)	rs78652302	0.00908
NM_004415.4(DSP):c.1481A>T (p.Tyr494Phe)	rs28763961	0.00618
NM_004415.4(DSP):c.4455G>T (p.Arg1485Ser)	rs113902911	0.00572
NM_004415.4(DSP):c.4588G>T (p.Val1530Phe)	rs141227126	0.00197
NM_004415.4(DSP):c.8455A>C (p.Met2819Leu)	rs138329459	0.00103
NM_004415.4(DSP):c.88G>A (p.Val30Met)	rs121912998	0.00094
NM_004415.4(DSP):c.8605A>G (p.Ile2869Val)	rs28763971	0.00077
NM_004415.4(DSP):c.2723G>A (p.Arg908His)	rs142494121	0.00041
NM_004415.4(DSP):c.688G>A (p.Asp230Asn)	rs147315869	0.00038
NM_004415.4(DSP):c.3923G>A (p.Arg1308Gln)	rs184154918	0.00037
NM_004415.4(DSP):c.7916G>A (p.Arg2639Gln)	rs116888866	0.00026
NM_004415.4(DSP):c.264C>T (p.Ile88=)	rs727502997	0.00004
NM_004415.4(DSP):c.1860G>A (p.Gln620=)	rs762658467	0.00001
NM_004415.4(DSP):c.8191T>C (p.Tyr2731His)	rs201397978	0.00001
NM_004415.4(DSP):c.12C>G (p.Asn4Lys)	rs368802003

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