"GeneDx"[submitter] AND "GPR179"[gene] - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 322963	NM_001004334.4(GPR179):c.7080T>G (p.Thr2360=)	GPR179	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 423230	NM_001004334.4(GPR179):c.6789del (p.Arg2264fs)	GPR179 (R2264fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 322975	NM_001004334.4(GPR179):c.5975G>A (p.Gly1992Asp)	GPR179 (G1992D)	Single nucleotide variant (missense variant)	Congenital stationary night blindness 1E +1 more	GConflicting classifications of pathogenicity
Select item 193823	NM_001004334.4(GPR179):c.5605C>G (p.Gln1869Glu)	GPR179 (Q1869E)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 322986	NM_001004334.4(GPR179):c.4306C>T (p.Arg1436Trp)	GPR179 (R1436W)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 385325	NM_001004334.4(GPR179):c.3454T>C (p.Ser1152Pro)	GPR179 (S1152P)	Single nucleotide variant (missense variant)	Congenital stationary night blindness 1E +2 more	GBenign/Likely benign
Select item 667427	NM_001004334.4(GPR179):c.3138_3139del (p.Glu1046fs)	GPR179 (E1046fs)	Microsatellite (frameshift variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 323008	NM_001004334.4(GPR179):c.2650C>T (p.Arg884Trp)	GPR179 (R884W)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1479710	NM_001004334.4(GPR179):c.2458G>C (p.Ala820Pro)	GPR179 (A820P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 426625	NM_001004334.4(GPR179):c.2427dup (p.Pro810fs)	GPR179 (P810fs)	Duplication (frameshift variant)	not provided	GConflicting classifications of pathogenicity
Select item 323013	NM_001004334.4(GPR179):c.2040C>T (p.Asp680=)	GPR179	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1234649	NM_001004334.4(GPR179):c.2038-202G>C	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235724	NM_001004334.4(GPR179):c.2037+44G>C	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1166893	NM_001004334.4(GPR179):c.1891-11=	GPR179	Variation (intron variant)	not provided	GBenign
Select item 1282411	NM_001004334.4(GPR179):c.1891-107G>A	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1240508	NM_001004334.4(GPR179):c.1891-221C>G	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224840	NM_001004334.4(GPR179):c.1890+210C>G	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248172	NM_001004334.4(GPR179):c.1890+74G>A	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294790	NM_001004334.4(GPR179):c.1785-237G>A	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249189	NM_001004334.4(GPR179):c.1784+121=	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273093	NM_001004334.4(GPR179):c.1646-76=	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1468356	NM_001004334.4(GPR179):c.1525A>G (p.Thr509Ala)	GPR179 (T509A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1294881	NM_001004334.4(GPR179):c.1407-157G>T	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262071	NM_001004334.4(GPR179):c.1406+109=	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276281	NM_001004334.4(GPR179):c.1406+98=	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264241	NM_001004334.4(GPR179):c.992-107=	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261346	NM_001004334.4(GPR179):c.991+97G>A	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1493118	NM_001004334.4(GPR179):c.988G>T (p.Gly330Trp)	GPR179 (G330W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 31204	NM_001004334.4(GPR179):c.984del (p.Ser329fs)	GPR179 (S329fs)	Deletion (frameshift variant)	Congenital stationary night blindness +4 more	GPathogenic
Select item 1287423	NM_001004334.4(GPR179):c.903+204A>C	GPR179	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262394	NM_001004334.4(GPR179):c.903+203del	GPR179	Deletion (intron variant)	not provided	GBenign
Select item 3367820	NM_001004334.4(GPR179):c.562C>A (p.Pro188Thr)	GPR179 (P188T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1482127	NM_001004334.4(GPR179):c.225T>A (p.Asn75Lys)	GPR179 (N75K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1358536	NM_001004334.4(GPR179):c.97C>T (p.Arg33Cys)	GPR179 (R33C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1279730	NM_001004334.4(GPR179):c.-123C>G	GPR179	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign

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Items: 35