List of variants in gene CPS1 reported as benign by Genome-Nilou Lab

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001875.5(CPS1):c.3337-79C>T	rs4673540	0.99993
NM_001875.5(CPS1):c.4101+62A>G	rs10932347	0.94113
NM_001875.5(CPS1):c.2679C>G (p.Gly893=)	rs2287599	0.64925
NM_001875.5(CPS1):c.1032C>T (p.Thr344=)	rs2229589	0.59558
NM_001122633.3(CPS1):c.-16+12G>A	rs17552879	0.43006
NM_001875.5(CPS1):c.3405-29A>T	rs3213784	0.37981
NM_001875.5(CPS1):c.4217C>A (p.Thr1406Asn)	rs1047891	0.33052
NM_001875.5(CPS1):c.3405-92G>T	rs34449727	0.29855
NM_001875.5(CPS1):c.3756+45C>T	rs6435580	0.24723
NM_001875.5(CPS1):c.2830-138C>T	rs2302908	0.24132
NM_001875.5(CPS1):c.2193-15G>T	rs2287600	0.09707
NM_001875.5(CPS1):c.2448C>T (p.Cys816=)	rs75395645	0.01788
NM_001875.5(CPS1):c.-4_-3insTTC	rs61509952
NM_001875.5(CPS1):c.1030A>G (p.Thr344Ala)	rs1047883
NM_001875.5(CPS1):c.3928-8del	rs397703682

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