ClinVar Miner

List of variants in gene GPR179 reported as pathogenic

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001004334.4(GPR179):c.724C>T (p.Arg242Ter) rs767509745 0.00004
NM_001004334.4(GPR179):c.659A>G (p.Tyr220Cys) rs281875236 0.00003
NM_001004334.4(GPR179):c.673C>T (p.Gln225Ter) rs747682469 0.00002
NM_001004334.4(GPR179):c.1429C>T (p.Arg477Ter) rs764877172 0.00001
NM_001004334.4(GPR179):c.1543C>T (p.Arg515Ter) rs980007216 0.00001
NM_001004334.4(GPR179):c.1573C>T (p.Arg525Ter) rs773022324 0.00001
NM_001004334.4(GPR179):c.598C>T (p.Arg200Ter) rs387907138 0.00001
NM_001004334.4(GPR179):c.1000del (p.Glu334fs)
NM_001004334.4(GPR179):c.1005del (p.Ser335fs)
NM_001004334.4(GPR179):c.1250del (p.Val417fs)
NM_001004334.4(GPR179):c.1368del (p.Phe456fs) rs1435030978
NM_001004334.4(GPR179):c.1667G>A (p.Trp556Ter)
NM_001004334.4(GPR179):c.166del (p.Ala56fs)
NM_001004334.4(GPR179):c.1706C>A (p.Ser569Ter)
NM_001004334.4(GPR179):c.1727del (p.Tyr576fs) rs1567725425
NM_001004334.4(GPR179):c.1784+1G>A rs773126191
NM_001004334.4(GPR179):c.1807C>T (p.His603Tyr) rs281875234
NM_001004334.4(GPR179):c.1818G>A (p.Trp606Ter) rs1268507778
NM_001004334.4(GPR179):c.1835_1836insTTTTTTTTTTTTTTTTTTTTNNNNNNNNNNTGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCCCTCCTCCTCTTCTT (p.Phe613_His614insPhePhePhePhePheXaaXaaXaaXaaAspLeuValIleArgProProArgProProLysValLeuGlyLeuGlnAlaTerPhe)
NM_001004334.4(GPR179):c.187del (p.Leu63fs) rs794726686
NM_001004334.4(GPR179):c.278del (p.Pro93fs) rs794726685
NM_001004334.4(GPR179):c.280dup (p.Ser94fs)
NM_001004334.4(GPR179):c.357dup (p.Glu120Ter)
NM_001004334.4(GPR179):c.416del (p.Glu139fs)
NM_001004334.4(GPR179):c.416dup (p.Asp141fs)
NM_001004334.4(GPR179):c.595A>T (p.Lys199Ter)
NM_001004334.4(GPR179):c.647dup (p.Ala217fs) rs886043388
NM_001004334.4(GPR179):c.779_780dup (p.Pro262fs) rs1567728372
NM_001004334.4(GPR179):c.799_803delinsTGATCTAC (p.Gln267_Val268delinsTer) rs886043488
NM_001004334.4(GPR179):c.839_842del (p.Asn280fs) rs1244415676
NM_001004334.4(GPR179):c.857del (p.Pro286fs) rs2144276592
NM_001004334.4(GPR179):c.958C>T (p.Arg320Ter)
NM_001004334.4(GPR179):c.984del (p.Ser329fs) rs770066665
NM_001004334.4(GPR179):c.9del (p.Arg4fs)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.