List of variants in gene CNGB3 reported as benign for blindness (disorder)

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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: 38

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HGVS	dbSNP	gnomAD frequency
NM_019098.4(CNGB3):c.*1881T>C	rs990193	0.91428
NM_019098.5(CNGB3):c.702T>G (p.Cys234Trp)	rs6471482	0.88912
NM_019098.5(CNGB3):c.892A>C (p.Thr298Pro)	rs4961206	0.64246
NM_019098.4(CNGB3):c.*1639C>A	rs990192	0.58635
NM_019098.5(CNGB3):c.852+55C>T	rs3735967	0.39180
NM_019098.5(CNGB3):c.1481-145A>C	rs13258590	0.33289
NM_019098.4(CNGB3):c.*1638G>A	rs28471019	0.09998
NM_019098.5(CNGB3):c.2264A>G (p.Glu755Gly)	rs3735972	0.08214
NM_019098.5(CNGB3):c.2214A>G (p.Glu738=)	rs3735970	0.08211
NM_019098.5(CNGB3):c.919A>G (p.Ile307Val)	rs13265557	0.05793
NM_019098.5(CNGB3):c.1356G>A (p.Gln452=)	rs34839859	0.05572
NM_019098.5(CNGB3):c.1179-38T>C	rs3735969	0.05147
NM_019098.5(CNGB3):c.608G>A (p.Arg203Gln)	rs16916632	0.05057
NM_019098.5(CNGB3):c.1781+10A>T	rs7000747	0.05032
NM_019098.5(CNGB3):c.211+13T>G	rs66881636	0.04794
NM_019098.5(CNGB3):c.*778T>C	rs16915859	0.01933
NM_019098.5(CNGB3):c.*389A>C	rs16915861	0.01929
NM_019098.5(CNGB3):c.595G>A (p.Glu199Lys)	rs114305748	0.01886
NM_019098.5(CNGB3):c.80A>G (p.Asn27Ser)	rs35807406	0.01728
NM_019098.5(CNGB3):c.354G>T (p.Pro118=)	rs75858066	0.01037
NM_019098.5(CNGB3):c.1397T>C (p.Met466Thr)	rs35010099	0.00978
NM_019098.5(CNGB3):c.1626C>T (p.Ser542=)	rs35903042	0.00786
NM_019098.5(CNGB3):c.212-3T>C	rs79126074	0.00635
NM_019098.5(CNGB3):c.1492T>A (p.Leu498Met)	rs115246141	0.00350
NM_019098.5(CNGB3):c.2420C>G (p.Ala807Gly)	rs142846289	0.00300
NM_019098.5(CNGB3):c.1405T>G (p.Tyr469Asp)	rs35365413	0.00248
NM_019098.5(CNGB3):c.1510A>G (p.Thr504Ala)	rs140286824	0.00065
NM_019098.5(CNGB3):c.494-11T>C	rs543970676	0.00062
NM_019098.5(CNGB3):c.1383C>T (p.Asp461=)	rs112847374	0.00039
NM_019098.5(CNGB3):c.2415A>C (p.Glu805Asp)	rs186448979	0.00025
NM_019098.5(CNGB3):c.*997A>G	rs141428300	0.00014
NM_019098.4(CNGB3):c.-36T>G	rs7812496
NM_019098.5(CNGB3):c.*1303G>A	rs17683284
NM_019098.5(CNGB3):c.*735A>G	rs73269601
NM_019098.5(CNGB3):c.*915G>C	rs189446254
NM_019098.5(CNGB3):c.2158CAAAAAGAAAATGAAGATAAA[1] (p.720QKENEDK[1])	rs746549330
NM_019098.5(CNGB3):c.339-10dup	rs200792506
NM_019098.5(CNGB3):c.494-11dup	rs36008065

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