ClinVar Miner

List of variants in gene GPR179 reported as likely benign by Ambry Genetics

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001004334.4(GPR179):c.1133C>T (p.Ala378Val) rs192426710 0.00128
NM_001004334.4(GPR179):c.2731G>A (p.Val911Met) rs201772198 0.00031
NM_001004334.4(GPR179):c.5812G>A (p.Asp1938Asn) rs202208376 0.00030
NM_001004334.4(GPR179):c.814G>A (p.Val272Ile) rs183799079 0.00030
NM_001004334.4(GPR179):c.6335C>T (p.Ala2112Val) rs542057732 0.00014
NM_001004334.4(GPR179):c.1220G>A (p.Arg407Gln) rs568763662 0.00008
NM_001004334.4(GPR179):c.6404C>T (p.Ala2135Val) rs577578718 0.00007
NM_001004334.4(GPR179):c.3914T>C (p.Met1305Thr) rs201583620 0.00006
NM_001004334.4(GPR179):c.17C>T (p.Ala6Val) rs758334393 0.00005
NM_001004334.4(GPR179):c.671C>T (p.Thr224Met) rs372101002 0.00002
NM_001004334.4(GPR179):c.941G>A (p.Arg314His) rs201014514 0.00002
NM_001004334.4(GPR179):c.3349G>A (p.Gly1117Arg) rs771334464 0.00001
NM_001004334.4(GPR179):c.1777A>G (p.Thr593Ala)
NM_001004334.4(GPR179):c.2230G>A (p.Gly744Ser)
NM_001004334.4(GPR179):c.3334G>A (p.Glu1112Lys)
NM_001004334.4(GPR179):c.4259C>T (p.Pro1420Leu)
NM_001004334.4(GPR179):c.431T>C (p.Val144Ala)
NM_001004334.4(GPR179):c.5272T>C (p.Trp1758Arg)
NM_001004334.4(GPR179):c.5303G>A (p.Gly1768Asp)

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