List of variants in gene UBA3 reported as uncertain significance for not specified

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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: 18

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HGVS	dbSNP	gnomAD frequency
NM_003968.4(UBA3):c.650T>A (p.Met217Lys)	rs144568523	0.00005
NM_003968.4(UBA3):c.467A>G (p.Tyr156Cys)	rs758067399	0.00003
NM_003968.4(UBA3):c.1334C>T (p.Ala445Val)	rs147779512	0.00002
NM_003968.4(UBA3):c.505A>G (p.Ile169Val)	rs368942872	0.00002
NM_003968.4(UBA3):c.793G>A (p.Gly265Arg)	rs1247802328	0.00002
NM_003968.4(UBA3):c.281G>C (p.Arg94Thr)	rs1306600084	0.00001
NM_003968.4(UBA3):c.734T>G (p.Leu245Arg)	rs1036325132	0.00001
NM_003968.4(UBA3):c.100T>C (p.Trp34Arg)
NM_003968.4(UBA3):c.1075G>A (p.Glu359Lys)
NM_003968.4(UBA3):c.1237C>A (p.Leu413Ile)
NM_003968.4(UBA3):c.1256C>T (p.Thr419Ile)
NM_003968.4(UBA3):c.1261A>G (p.Ile421Val)
NM_003968.4(UBA3):c.1387T>G (p.Ser463Ala)	rs2471738012
NM_003968.4(UBA3):c.415T>G (p.Cys139Gly)	rs796784390
NM_003968.4(UBA3):c.663C>G (p.Ile221Met)
NM_003968.4(UBA3):c.778A>C (p.Lys260Gln)
NM_003968.4(UBA3):c.916G>C (p.Val306Leu)	rs2091982491
NM_003968.4(UBA3):c.943T>C (p.Ser315Pro)

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