List of variants reported as benign for Amyotrophic lateral sclerosis type 15

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_013444.4(UBQLN2):c.1461C>A (p.Thr487=)	rs45559331	0.00516
NM_013444.4(UBQLN2):c.1383G>A (p.Gly461=)	rs142250604	0.00313
NM_013444.4(UBQLN2):c.-163G>T	rs192883799	0.00010
NM_013444.4(UBQLN2):c.51T>A (p.Pro17=)	rs371163085	0.00010
NM_013444.4(UBQLN2):c.1302G>T (p.Leu434=)	rs759543866	0.00007
NM_013444.4(UBQLN2):c.579C>T (p.Ser193=)	rs768910794	0.00006
NM_013444.4(UBQLN2):c.1573C>T (p.Pro525Ser)	rs369947678	0.00005
NM_013444.4(UBQLN2):c.1715C>T (p.Ala572Val)	rs772368310	0.00005
NM_013444.4(UBQLN2):c.1734A>G (p.Pro578=)	rs1271440811	0.00001
NM_013444.4(UBQLN2):c.717G>A (p.Arg239=)	rs762742451	0.00001
NM_013444.4(UBQLN2):c.1173C>T (p.Tyr391=)
NM_013444.4(UBQLN2):c.1464T>C (p.Ala488=)
NM_013444.4(UBQLN2):c.1491CATAGGCCC[1] (p.499GPI[1])
NM_013444.4(UBQLN2):c.1752A>C (p.Gln584His)
NM_013444.4(UBQLN2):c.327G>C (p.Gln109His)
NM_013444.4(UBQLN2):c.359G>C (p.Gly120Ala)
NM_013444.4(UBQLN2):c.405T>C (p.Pro135=)
NM_013444.4(UBQLN2):c.834G>C (p.Pro278=)

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