List of variants in gene NOD1 reported as not provided by Human Evolutionary Genetics, Institut Pasteur

Minimum submission review status:		Collection method:
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: 28

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HGVS	dbSNP	gnomAD frequency
NM_001354849.1(NOD1):c.-585G>C	rs199475895	0.00532
NM_006092.3(NOD1):c.-523-629C>T	rs199475893	0.00087
NM_006092.4(NOD1):c.2201+36C>T	rs199476264	0.00016
NM_006092.4(NOD1):c.2285+220T>A	rs199476270	0.00014
NM_006092.4(NOD1):c.2537+169A>C	rs199476273	0.00013
NM_006092.4(NOD1):c.254T>A (p.Phe85Tyr)	rs199475897	0.00011
NM_006092.4(NOD1):c.-121-85G>C	rs199476262	0.00009
NM_006092.4(NOD1):c.-234G>A	rs199475896	0.00007
NM_006092.4(NOD1):c.1458C>T (p.Ser486=)	rs199475902	0.00006
NM_006092.4(NOD1):c.2285+90G>A	rs199476267	0.00004
NM_006092.4(NOD1):c.1423C>T (p.Leu475Phe)	rs199475901	0.00003
NM_006092.4(NOD1):c.2285+118C>T	rs199476269	0.00003
NM_006092.4(NOD1):c.2285+31T>C	rs199476266	0.00003
NM_006092.4(NOD1):c.285T>C (p.Asp95=)	rs199475898	0.00003
NM_006092.4(NOD1):c.2202-27C>T	rs199476265	0.00002
NM_006092.4(NOD1):c.1369C>T (p.Arg457Trp)	rs199475900	0.00001
NM_006092.4(NOD1):c.2454-116G>C	rs199476271	0.00001
NM_006092.3(NOD1):c.-523-142G>A	rs199475894
NM_006092.4(NOD1):c.-211+198G>A	rs199476261
NM_006092.4(NOD1):c.1492del (p.Leu498fs)	rs199476263
NM_006092.4(NOD1):c.2080G>A (p.Ala694Thr)	rs199475903
NM_006092.4(NOD1):c.2285+112G>A	rs199476268
NM_006092.4(NOD1):c.2285+372T>A	rs199475904
NM_006092.4(NOD1):c.2537+344C>G	rs199476274
NM_006092.4(NOD1):c.2537+394T>A	rs199476275
NM_006092.4(NOD1):c.2537+81G>A	rs199476272
NM_006092.4(NOD1):c.2697G>C (p.Lys899Asn)	rs199475905
NM_006092.4(NOD1):c.375A>G (p.Pro125=)	rs199475899

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