ClinVar Miner

List of variants in gene GPR179 reported as likely benign for congenital stationary night blindness 1E

Included ClinVar conditions (1):
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Gene type:
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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_001004334.4(GPR179):c.2040C>T (p.Asp680=) rs111770829 0.02523
NM_001004334.4(GPR179):c.654T>G (p.Asp218Glu) rs74871223 0.01200
NM_001004334.4(GPR179):c.74C>A (p.Ala25Asp) rs111677298 0.01196
NM_001004334.4(GPR179):c.3454T>C (p.Ser1152Pro) rs149252987 0.00689
NM_001004334.4(GPR179):c.2604G>C (p.Glu868Asp) rs201214109 0.00473
NM_001004334.4(GPR179):c.3847C>T (p.Pro1283Ser) rs150125328 0.00382
NM_001004334.4(GPR179):c.6336G>A (p.Ala2112=) rs186214845 0.00296
NM_001004334.4(GPR179):c.5563C>G (p.Leu1855Val) rs79954845 0.00280
NM_001004334.4(GPR179):c.4709C>T (p.Thr1570Met) rs187512697 0.00241
NM_001004334.4(GPR179):c.4306C>T (p.Arg1436Trp) rs147966258 0.00228
NM_001004334.4(GPR179):c.5019C>G (p.Thr1673=) rs182907807 0.00219
NM_001004334.4(GPR179):c.959G>A (p.Arg320Gln) rs189931659 0.00194
NM_001004334.4(GPR179):c.1029C>T (p.Phe343=) rs149830172 0.00183
NM_001004334.4(GPR179):c.5975G>A (p.Gly1992Asp) rs200936863 0.00160
NM_001004334.4(GPR179):c.657A>T (p.Gly219=) rs116896787 0.00141
NM_001004334.4(GPR179):c.61G>C (p.Val21Leu) rs150616884 0.00120
NM_001004334.4(GPR179):c.725G>A (p.Arg242Gln) rs143624972 0.00120
NM_001004334.4(GPR179):c.3441C>T (p.Ser1147=) rs377711366 0.00054
NM_001004334.4(GPR179):c.795-4G>A rs150772690 0.00038
NM_001004334.4(GPR179):c.4381G>C (p.Glu1461Gln) rs201149338 0.00037
NM_001004334.4(GPR179):c.627C>T (p.Leu209=) rs143660134 0.00024
NM_001004334.4(GPR179):c.3726G>A (p.Glu1242=) rs118133878 0.00019
NM_001004334.4(GPR179):c.3426C>T (p.Ala1142=) rs371169614 0.00009
NM_001004334.4(GPR179):c.619G>C (p.Gly207Arg) rs1329542100 0.00002
NM_001004334.4(GPR179):c.3819C>G (p.Ala1273=) rs201777145
NM_001004334.4(GPR179):c.4888G>C (p.Glu1630Gln) rs149998444
NM_001004334.4(GPR179):c.6494C>A (p.Thr2165Lys) rs114844749

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