List of variants in gene SPG11 studied for Charcot-Marie-Tooth disease

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP
NM_025137.4(SPG11):c.1085G>A (p.Trp362Ter)	rs140385286
NM_025137.4(SPG11):c.118C>T (p.Gln40Ter)	rs267607084
NM_025137.4(SPG11):c.1621C>T (p.Gln541Ter)	rs765061840
NM_025137.4(SPG11):c.3425C>G (p.Ser1142Cys)	rs201082396
NM_025137.4(SPG11):c.5199del (p.Lys1733fs)	rs779268551
NM_025137.4(SPG11):c.524_528ATATT[1] (p.Ile177fs)	rs312262716
NM_025137.4(SPG11):c.5471G>A (p.Arg1824Gln)	rs752401008
NM_025137.4(SPG11):c.592C>T (p.Gln198Ter)	rs863225440
NM_025137.4(SPG11):c.6043G>A (p.Asp2015Asn)	rs771242219
NM_025137.4(SPG11):c.604A>G (p.Met202Val)	rs201875705
NM_025137.4(SPG11):c.6100C>T (p.Arg2034Ter)	rs118203963
NM_025137.4(SPG11):c.6625C>T (p.Arg2209Cys)	rs374057859
NM_025137.4(SPG11):c.6632dup (p.Pro2212fs)	rs863225439
NM_025137.4(SPG11):c.6899T>C (p.Leu2300Pro)	rs371334506

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