List of variants in gene SPG7 reported by Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg

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

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_003119.4(SPG7):c.1529C>T (p.Ala510Val)	rs61755320	0.00361
NM_003119.4(SPG7):c.1045G>A (p.Gly349Ser)	rs141659620	0.00103
NM_003119.4(SPG7):c.1933T>A (p.Ser645Thr)	rs2099104	0.00073
NM_003119.4(SPG7):c.233T>A (p.Leu78Ter)	rs121918358	0.00014
NM_003119.4(SPG7):c.619C>T (p.Arg207Trp)	rs199751531	0.00010
NM_003119.4(SPG7):c.1235C>T (p.Ala412Val)	rs746668495	0.00001
NM_003119.4(SPG7):c.1048C>G (p.Pro350Ala)	rs199789849
NM_003119.4(SPG7):c.2219A>G (p.Tyr740Cys)
NM_003119.4(SPG7):c.694del (p.Glu232fs)

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