List of variants in gene GPR179 reported as likely benign for blindness (disorder)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_001004334.4(GPR179):c.2040C>T (p.Asp680=)	rs111770829	0.02332
NM_001004334.4(GPR179):c.654T>G (p.Asp218Glu)	rs74871223	0.01135
NM_001004334.4(GPR179):c.74C>A (p.Ala25Asp)	rs111677298	0.01132
NM_001004334.4(GPR179):c.3454T>C (p.Ser1152Pro)	rs149252987	0.00640
NM_001004334.4(GPR179):c.2604G>C (p.Glu868Asp)	rs201214109	0.00473
NM_001004334.4(GPR179):c.3847C>T (p.Pro1283Ser)	rs150125328	0.00373
NM_001004334.4(GPR179):c.6336G>A (p.Ala2112=)	rs186214845	0.00287
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.4306C>T (p.Arg1436Trp)	rs147966258	0.00216
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	0.00130
NM_001004334.4(GPR179):c.725G>A (p.Arg242Gln)	rs143624972	0.00120
NM_001004334.4(GPR179):c.61G>C (p.Val21Leu)	rs150616884	0.00115
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	0.00028
NM_001004334.4(GPR179):c.3426C>T (p.Ala1142=)	rs371169614	0.00025
NM_001004334.4(GPR179):c.3726G>A (p.Glu1242=)	rs118133878	0.00021
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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