List of variants in gene ACE reported as benign by Illumina Laboratory Services, Illumina

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: 39

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HGVS	dbSNP	gnomAD frequency
NM_000789.4(ACE):c.*910A>G	rs1055086	0.59649
NM_000789.4(ACE):c.2328G>A (p.Thr776=)	rs4343	0.56401
NM_000789.4(ACE):c.3387T>C (p.Phe1129=)	rs4362	0.51177
NM_000789.4(ACE):c.3692-6G>A	rs4363	0.50850
NM_000789.4(ACE):c.2193A>G (p.Ala731=)	rs4331	0.46564
NM_000789.4(ACE):c.2306-11A>C	rs4342	0.45325
NM_000789.4(ACE):c.1215C>T (p.Pro405=)	rs4309	0.35804
NM_000789.4(ACE):c.582C>T (p.Asn194=)	rs4298	0.15457
NM_000789.4(ACE):c.655+13C>T	rs4300	0.05754
NM_000789.4(ACE):c.3380+5C>T	rs12720737	0.03115
NM_000789.4(ACE):c.781G>T (p.Ala261Ser)	rs4303	0.02833
NM_000789.4(ACE):c.3906G>A (p.Glu1302=)	rs4365	0.02561
NM_000789.4(ACE):c.*709G>A	rs112901380	0.01965
NM_000789.4(ACE):c.3691+5C>T	rs12720744	0.01507
NM_000789.4(ACE):c.*586C>A	rs74979666	0.01148
NM_000789.4(ACE):c.731A>G (p.Tyr244Cys)	rs3730025	0.01121
NM_000789.4(ACE):c.1119-8C>T	rs114861086	0.00991
NM_000789.4(ACE):c.2787C>T (p.Thr929=)	rs4348	0.00917
NM_000789.4(ACE):c.780C>T (p.Arg260=)	rs4302	0.00838
NM_000789.4(ACE):c.975G>T (p.Val325=)	rs61738840	0.00783
NM_000789.4(ACE):c.970C>T (p.Arg324Trp)	rs35141294	0.00781
NM_000789.4(ACE):c.1060G>A (p.Gly354Arg)	rs56394458	0.00732
NM_000789.4(ACE):c.656-9C>T	rs12720734	0.00679
NM_000789.4(ACE):c.847+12G>A	rs12709422	0.00678
NM_000789.4(ACE):c.2382G>A (p.Ala794=)	rs61738817	0.00669
NM_000789.4(ACE):c.2187G>T (p.Arg729=)	rs35553988	0.00661
NM_000789.4(ACE):c.*505C>G	rs111618613	0.00648
NM_000789.4(ACE):c.2550C>G (p.Leu850=)	rs4975	0.00609
NM_000789.4(ACE):c.*894G>A	rs78716020	0.00555
NM_000789.4(ACE):c.417+8G>A	rs114000559	0.00400
NM_000789.4(ACE):c.1681C>T (p.Arg561Trp)	rs4314	0.00316
NM_000789.4(ACE):c.479A>G (p.Asn160Ser)	rs117134739	0.00056
NM_000789.4(ACE):c.5G>T (p.Gly2Val)	rs558593002	0.00053
NM_000789.4(ACE):c.460G>A (p.Ala154Thr)	rs13306087	0.00044
NM_000789.4(ACE):c.2791C>T (p.Leu931=)	rs141180606	0.00013
NM_000789.4(ACE):c.*728CT[3]	rs4366
NM_000789.4(ACE):c.1341G>C (p.Thr447=)	rs34241302
NM_000789.4(ACE):c.2518C>A (p.Arg840=)	rs3730036
NM_000789.4(ACE):c.3856C>A (p.Arg1286Ser)	rs4364

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