ClinVar Miner

List of variants in gene GPR179 reported by Eurofins NTD LLC (GA)

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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_001004334.4(GPR179):c.909= (p.Val303=) rs9894059 0.24635
NM_001004334.4(GPR179):c.5605C>G (p.Gln1869Glu) rs4399578 0.05465
NM_001004334.4(GPR179):c.1478= (p.His493=) rs4550493 0.04915
NM_001004334.4(GPR179):c.2392G>A (p.Ala798Thr) rs78470373 0.01044
NM_001004334.4(GPR179):c.3454T>C (p.Ser1152Pro) rs149252987 0.00689
NM_001004334.4(GPR179):c.3847C>T (p.Pro1283Ser) rs150125328 0.00382
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.5019C>G (p.Thr1673=) rs182907807 0.00219
NM_001004334.4(GPR179):c.959G>A (p.Arg320Gln) rs189931659 0.00194
NM_001004334.4(GPR179):c.5975G>A (p.Gly1992Asp) rs200936863 0.00160
NM_001004334.4(GPR179):c.3401G>A (p.Arg1134Gln) rs112987826 0.00113
NM_001004334.4(GPR179):c.5982C>T (p.Ala1994=) rs185715311 0.00079
NM_001004334.4(GPR179):c.2410C>T (p.Arg804Trp) rs201086495 0.00063
NM_001004334.4(GPR179):c.3970G>A (p.Glu1324Lys) rs201039021 0.00027
NM_001004334.4(GPR179):c.3568C>T (p.Arg1190Trp) rs200978744 0.00016
NM_001004334.4(GPR179):c.5058C>T (p.Ala1686=) rs376750375 0.00014
NM_001004334.4(GPR179):c.1220G>A (p.Arg407Gln) rs568763662 0.00008
NM_001004334.4(GPR179):c.5983G>A (p.Ala1995Thr) rs749758071 0.00008
NM_001004334.4(GPR179):c.673C>T (p.Gln225Ter) rs747682469 0.00002
NM_001004334.4(GPR179):c.1484G>A (p.Gly495Glu) rs794727848 0.00001
NM_001004334.4(GPR179):c.1543C>T (p.Arg515Ter) rs980007216 0.00001
NM_001004334.4(GPR179):c.320A>G (p.Asn107Ser) rs886043746 0.00001
NM_001004334.4(GPR179):c.415G>A (p.Glu139Lys) rs370341548 0.00001
NM_001004334.4(GPR179):c.1228A>G (p.Arg410Gly) rs776824900
NM_001004334.4(GPR179):c.1304T>C (p.Ile435Thr) rs1567726068
NM_001004334.4(GPR179):c.4217dup (p.Gln1407fs) rs886044423
NM_001004334.4(GPR179):c.4888G>C (p.Glu1630Gln) rs149998444
NM_001004334.4(GPR179):c.582C>A (p.Thr194=) rs756762102
NM_001004334.4(GPR179):c.647dup (p.Ala217fs) rs886043388
NM_001004334.4(GPR179):c.799_803delinsTGATCTAC (p.Gln267_Val268delinsTer) rs886043488

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