List of variants in gene DYSF reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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_001130987.2(DYSF):c.5503C>T (p.Arg1835Trp)	rs139879284	0.00161
NM_001130987.2(DYSF):c.2956A>T (p.Met986Leu)	rs144636654	0.00112
NM_001130987.2(DYSF):c.4021C>G (p.Gln1341Glu)	rs147950418	0.00094
NM_001130987.2(DYSF):c.2335G>A (p.Gly779Ser)	rs138654170	0.00082
NM_001130987.2(DYSF):c.4694A>C (p.Lys1565Thr)	rs76086153	0.00080
NM_001130987.2(DYSF):c.4859G>A (p.Arg1620His)	rs185596534	0.00072
NM_001130987.2(DYSF):c.5266C>T (p.Arg1756Trp)	rs148541407	0.00071
NM_001130987.2(DYSF):c.4627G>A (p.Val1543Ile)	rs143895253	0.00055
NM_001130987.2(DYSF):c.4597T>C (p.Tyr1533His)	rs150139276	0.00034
NM_001130987.2(DYSF):c.3002A>C (p.Lys1001Thr)	rs34061568	0.00031
NM_001130987.2(DYSF):c.350C>T (p.Ser117Leu)	rs199677396	0.00018
NM_001130987.2(DYSF):c.5102C>T (p.Thr1701Met)	rs143059463	0.00016
NM_001130987.2(DYSF):c.2855C>T (p.Pro952Leu)	rs150717638	0.00014
NM_001130987.2(DYSF):c.5276G>A (p.Arg1759His)	rs147678255	0.00014
NM_001130987.2(DYSF):c.3139C>G (p.Pro1047Ala)	rs1358370392	0.00013
NM_001130987.2(DYSF):c.3541G>A (p.Asp1181Asn)	rs139194093	0.00013
NM_001130987.2(DYSF):c.6320C>T (p.Pro2107Leu)	rs149732545	0.00012
NM_001130987.2(DYSF):c.4252C>G (p.Pro1418Ala)	rs151268930	0.00009
NM_001130987.2(DYSF):c.2974G>A (p.Asp992Asn)	rs200422222	0.00006
NM_001130987.2(DYSF):c.6035C>T (p.Ala2012Val)	rs201784424	0.00006
NM_001130987.2(DYSF):c.4358C>T (p.Ala1453Val)	rs754979997	0.00004
NM_001130987.2(DYSF):c.3851C>T (p.Pro1284Leu)	rs761916273	0.00002
NM_001130987.2(DYSF):c.5269A>C (p.Thr1757Pro)	rs746919714	0.00002
NM_001130987.2(DYSF):c.3805C>T (p.Arg1269Trp)	rs753817458	0.00001
NM_001130987.2(DYSF):c.5107G>A (p.Val1703Ile)	rs747210644	0.00001
NM_001130987.2(DYSF):c.1280A>C (p.Asp427Ala)	rs1553531687
NM_001130987.2(DYSF):c.3678C>G (p.Ile1226Met)	rs148858485
NM_001130987.2(DYSF):c.4244A>C (p.Tyr1415Ser)	rs775254512
NM_001130987.2(DYSF):c.4982C>T (p.Thr1661Met)	rs144383140
NM_001130987.2(DYSF):c.5146C>T (p.Arg1716Cys)	rs771735871
NM_001130987.2(DYSF):c.6347A>T (p.Lys2116Met)
NM_001130987.2(DYSF):c.947T>C (p.Ile316Thr)	rs1553522164
NM_001130987.2(DYSF):c.981T>G (p.Asp327Glu)
NM_001130987.2(DYSF):c.98A>G (p.Lys33Arg)	rs539484245

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