ClinVar Miner

Variants in gene GPR179 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 25
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HGVS dbSNP gnomAD frequency
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.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.5089T>G (p.Leu1697Val) rs202030098 0.00193
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.1133C>T (p.Ala378Val) rs192426710 0.00128
NM_001004334.4(GPR179):c.61G>C (p.Val21Leu) rs150616884 0.00120
NM_001004334.4(GPR179):c.7014G>A (p.Ser2338=) rs184147344 0.00071
NM_001004334.4(GPR179):c.2410C>T (p.Arg804Trp) rs201086495 0.00063
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.3900A>T (p.Ile1300=) rs200167781 0.00021
NM_001004334.4(GPR179):c.1140G>A (p.Leu380=) rs201053760 0.00010
NM_001004334.4(GPR179):c.3426C>T (p.Ala1142=) rs371169614 0.00009
NM_001004334.4(GPR179):c.5905G>A (p.Val1969Ile) rs144104172 0.00009
NM_001004334.4(GPR179):c.1839C>T (p.Phe613=) rs746417155 0.00008
NM_001004334.4(GPR179):c.4188A>G (p.Gln1396=) rs201368251 0.00006
NM_001004334.4(GPR179):c.3819C>G (p.Ala1273=) rs201777145
NM_001004334.4(GPR179):c.4888G>C (p.Glu1630Gln) rs149998444

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