List of variants in gene DSP reported as uncertain significance by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.2596C>T (p.Arg866Cys)	rs142429411	0.00214
NM_004415.4(DSP):c.4489C>T (p.Arg1497Trp)	rs148041814	0.00178
NM_004415.4(DSP):c.4372C>G (p.Arg1458Gly)	rs28763965	0.00131
NM_004415.4(DSP):c.5218G>A (p.Glu1740Lys)	rs142885240	0.00091
NM_004415.4(DSP):c.6881C>G (p.Ala2294Gly)	rs147000526	0.00062
NM_004415.4(DSP):c.5167G>C (p.Glu1723Gln)	rs142803672	0.00041
NM_004415.4(DSP):c.889G>A (p.Asp297Asn)	rs201930322	0.00014
NM_004415.4(DSP):c.2774G>A (p.Arg925Gln)	rs139799237	0.00013
NM_004415.4(DSP):c.5744G>A (p.Arg1915His)	rs146617683	0.00011
NM_004415.4(DSP):c.5063C>T (p.Ala1688Val)	rs372288373	0.00005
NM_004415.4(DSP):c.5555G>A (p.Arg1852His)	rs193922669	0.00005
NM_004415.4(DSP):c.4490G>A (p.Arg1497Gln)	rs727505037	0.00004
NM_004415.4(DSP):c.5173C>T (p.Arg1725Trp)	rs200336897	0.00004
NM_004415.4(DSP):c.3661A>G (p.Ile1221Val)	rs794728120	0.00002
NM_004415.4(DSP):c.3774C>A (p.Asp1258Glu)	rs748733750	0.00002
NM_004415.4(DSP):c.249G>A (p.Met83Ile)	rs1426930663	0.00001
NM_004415.4(DSP):c.4405C>T (p.Leu1469Phe)	rs752121953	0.00001
NM_004415.4(DSP):c.6956G>A (p.Gly2319Asp)	rs762943687	0.00001
NM_004415.4(DSP):c.8309A>G (p.Tyr2770Cys)	rs371020228	0.00001
NM_004415.4(DSP):c.1350_1351insTTA (p.Pro450_Arg451insLeu)	rs1581802595
NM_004415.4(DSP):c.1357C>T (p.Pro453Ser)	rs1554106845
NM_004415.4(DSP):c.2894T>C (p.Leu965Pro)	rs1581813405
NM_004415.4(DSP):c.3764G>A (p.Arg1255Lys)	rs777407386
NM_004415.4(DSP):c.4541T>C (p.Leu1514Pro)	rs1173680775
NM_004415.4(DSP):c.557A>T (p.His186Leu)	rs1033990351
NM_004415.4(DSP):c.7503_7508del (p.Cys2501_Glu2502del)	rs1473818298
NM_004415.4(DSP):c.7850G>A (p.Ser2617Asn)	rs766739838
NM_004415.4(DSP):c.8496ATCTCGCTCCGG[1] (p.2827SGSR[4])	rs397516971
NM_004415.4(DSP):c.877G>A (p.Glu293Lys)	rs876657799

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