List of variants in gene NOG reported as pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 17q22(chr17:54671585-54672283)x1
NM_005450.6(NOG):c.103C>T (p.Pro35Ser)	rs28937580
NM_005450.6(NOG):c.104C>G (p.Pro35Arg)	rs104894611
NM_005450.6(NOG):c.328C>T (p.Gln110Ter)	rs104894614
NM_005450.6(NOG):c.355G>T (p.Glu119Ter)	rs2052469986
NM_005450.6(NOG):c.449G>A (p.Trp150Ter)
NM_005450.6(NOG):c.509C>T (p.Pro170Leu)	rs2052471344
NM_005450.6(NOG):c.551G>C (p.Cys184Ser)
NM_005450.6(NOG):c.613T>G (p.Trp205Gly)
NM_005450.6(NOG):c.621T>A (p.Cys207Ter)
NM_005450.6(NOG):c.665A>G (p.Tyr222Cys)	rs104894602

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