ClinVar Miner

List of variants in gene GPR179 reported as uncertain significance for congenital stationary night blindness

Included ClinVar conditions (26):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 130
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001004334.4(GPR179):c.*824G>A rs191828655 0.00537
NM_001004334.4(GPR179):c.*554C>T rs138942149 0.00319
NM_001004334.4(GPR179):c.959G>A (p.Arg320Gln) rs189931659 0.00194
NM_001004334.4(GPR179):c.1133C>T (p.Ala378Val) rs192426710 0.00128
NM_001004334.4(GPR179):c.2895G>A (p.Leu965=) rs200583958 0.00096
NM_001004334.4(GPR179):c.5868C>T (p.Ser1956=) rs202228440 0.00082
NM_001004334.4(GPR179):c.5982C>T (p.Ala1994=) rs185715311 0.00079
NM_001004334.4(GPR179):c.976G>A (p.Ala326Thr) rs201963254 0.00067
NM_001004334.4(GPR179):c.991+4T>C rs375898051 0.00067
NM_001004334.4(GPR179):c.2410C>T (p.Arg804Trp) rs201086495 0.00063
NM_001004334.4(GPR179):c.5416G>A (p.Ala1806Thr) rs201654499 0.00054
NM_001004334.4(GPR179):c.973G>A (p.Gly325Arg) rs200392643 0.00054
NM_001004334.4(GPR179):c.6475A>G (p.Lys2159Glu) rs181844178 0.00049
NM_001004334.4(GPR179):c.1723C>T (p.Arg575Cys) rs200801090 0.00043
NM_001004334.4(GPR179):c.691C>T (p.Pro231Ser) rs200731095 0.00043
NM_001004334.4(GPR179):c.1533C>T (p.Gly511=) rs200421731 0.00039
NM_001004334.4(GPR179):c.3752C>T (p.Ser1251Leu) rs368643450 0.00034
NM_001004334.4(GPR179):c.5927G>A (p.Arg1976His) rs200274687 0.00031
NM_001004334.4(GPR179):c.3656_3657del (p.Pro1219fs) rs779266036 0.00028
NM_001004334.4(GPR179):c.989G>T (p.Gly330Val) rs372908857 0.00025
NM_001004334.4(GPR179):c.*453C>T rs539092082 0.00021
NM_001004334.4(GPR179):c.3900A>T (p.Ile1300=) rs200167781 0.00021
NM_001004334.4(GPR179):c.*454G>A rs138028812 0.00019
NM_001004334.4(GPR179):c.3508C>T (p.Arg1170Trp) rs201856624 0.00019
NM_001004334.4(GPR179):c.5606A>C (p.Gln1869Pro) rs201516786 0.00019
NM_001004334.4(GPR179):c.5083G>A (p.Glu1695Lys) rs199697891 0.00017
NM_001004334.4(GPR179):c.3568C>T (p.Arg1190Trp) rs200978744 0.00016
NM_001004334.4(GPR179):c.5859G>A (p.Glu1953=) rs370586289 0.00016
NM_001004334.4(GPR179):c.5058C>T (p.Ala1686=) rs376750375 0.00014
NM_001004334.4(GPR179):c.6335C>T (p.Ala2112Val) rs542057732 0.00014
NM_001004334.4(GPR179):c.1784+8C>T rs137860025 0.00013
NM_001004334.4(GPR179):c.3145G>A (p.Ala1049Thr) rs188307315 0.00013
NM_001004334.4(GPR179):c.2248T>A (p.Ser750Thr) rs772088402 0.00010
NM_001004334.4(GPR179):c.3348C>T (p.Ser1116=) rs78284900 0.00010
NM_001004334.4(GPR179):c.5350C>A (p.Pro1784Thr) rs117255299 0.00010
NM_001004334.4(GPR179):c.4459G>A (p.Val1487Met) rs187514572 0.00009
NM_001004334.4(GPR179):c.5382G>A (p.Met1794Ile) rs199726938 0.00009
NM_001004334.4(GPR179):c.5905G>A (p.Val1969Ile) rs144104172 0.00009
NM_001004334.4(GPR179):c.1220G>A (p.Arg407Gln) rs568763662 0.00008
NM_001004334.4(GPR179):c.3383G>A (p.Arg1128Gln) rs370214602 0.00008
NM_001004334.4(GPR179):c.4047G>A (p.Ala1349=) rs201461684 0.00007
NM_001004334.4(GPR179):c.1217G>A (p.Arg406His) rs770208418 0.00006
NM_001004334.4(GPR179):c.2809G>A (p.Val937Ile) rs765764314 0.00006
NM_001004334.4(GPR179):c.3400C>T (p.Arg1134Trp) rs376874534 0.00006
NM_001004334.4(GPR179):c.3806C>T (p.Thr1269Met) rs754266923 0.00006
NM_001004334.4(GPR179):c.4188A>G (p.Gln1396=) rs201368251 0.00006
NM_001004334.4(GPR179):c.4739C>T (p.Pro1580Leu) rs778263955 0.00006
NM_001004334.4(GPR179):c.983C>T (p.Pro328Leu) rs370808770 0.00006
NM_001004334.4(GPR179):c.1441C>T (p.Arg481Trp) rs374449680 0.00005
NM_001004334.4(GPR179):c.3411G>A (p.Ala1137=) rs539071271 0.00005
NM_001004334.4(GPR179):c.522C>T (p.Ile174=) rs377062748 0.00005
NM_001004334.4(GPR179):c.1589G>A (p.Ser530Asn) rs371905233 0.00004
NM_001004334.4(GPR179):c.7035C>T (p.Gly2345=) rs368426715 0.00004
NM_001004334.4(GPR179):c.*304A>G rs541537671 0.00003
NM_001004334.4(GPR179):c.*522C>T rs147084359 0.00003
NM_001004334.4(GPR179):c.131C>A (p.Pro44Gln) rs376962885 0.00003
NM_001004334.4(GPR179):c.1466G>A (p.Arg489Gln) rs551972571 0.00003
NM_001004334.4(GPR179):c.2332C>T (p.Arg778Cys) rs759512521 0.00003
NM_001004334.4(GPR179):c.2348C>T (p.Pro783Leu) rs200492514 0.00003
NM_001004334.4(GPR179):c.5774T>G (p.Phe1925Cys) rs770905475 0.00003
NM_001004334.4(GPR179):c.6351G>A (p.Trp2117Ter) rs766582295 0.00003
NM_001004334.4(GPR179):c.659A>G (p.Tyr220Cys) rs281875236 0.00003
NM_001004334.4(GPR179):c.2150G>A (p.Arg717His) rs757722345 0.00002
NM_001004334.4(GPR179):c.2581G>A (p.Glu861Lys) rs756212907 0.00002
NM_001004334.4(GPR179):c.274C>A (p.Pro92Thr) rs1331610447 0.00002
NM_001004334.4(GPR179):c.3442G>A (p.Asp1148Asn) rs202183326 0.00002
NM_001004334.4(GPR179):c.4180C>G (p.Pro1394Ala) rs371158139 0.00002
NM_001004334.4(GPR179):c.4555G>A (p.Glu1519Lys) rs201569873 0.00002
NM_001004334.4(GPR179):c.5627G>C (p.Trp1876Ser) rs1290248528 0.00002
NM_001004334.4(GPR179):c.663G>T (p.Val221=) rs547308706 0.00002
NM_001004334.4(GPR179):c.*359C>G rs143494935 0.00001
NM_001004334.4(GPR179):c.1070T>C (p.Leu357Pro) rs747110718 0.00001
NM_001004334.4(GPR179):c.1417C>T (p.Leu473=) rs762389933 0.00001
NM_001004334.4(GPR179):c.1785-3C>T rs1394125999 0.00001
NM_001004334.4(GPR179):c.180C>T (p.Leu60=) rs770286670 0.00001
NM_001004334.4(GPR179):c.1947C>T (p.Asp649=) rs372049950 0.00001
NM_001004334.4(GPR179):c.2149C>T (p.Arg717Cys) rs767911479 0.00001
NM_001004334.4(GPR179):c.272T>C (p.Leu91Pro) rs867417666 0.00001
NM_001004334.4(GPR179):c.296C>T (p.Ala99Val) rs201405656 0.00001
NM_001004334.4(GPR179):c.3110T>C (p.Val1037Ala) rs2037343188 0.00001
NM_001004334.4(GPR179):c.3349G>A (p.Gly1117Arg) rs771334464 0.00001
NM_001004334.4(GPR179):c.3357G>A (p.Ala1119=) rs547577586 0.00001
NM_001004334.4(GPR179):c.3447C>T (p.Asp1149=) rs1262445850 0.00001
NM_001004334.4(GPR179):c.3466C>G (p.Gln1156Glu) rs1184314233 0.00001
NM_001004334.4(GPR179):c.4071G>A (p.Lys1357=) rs1168693630 0.00001
NM_001004334.4(GPR179):c.4810G>T (p.Glu1604Ter) rs1464221989 0.00001
NM_001004334.4(GPR179):c.489C>T (p.Ala163=) rs749471277 0.00001
NM_001004334.4(GPR179):c.4996C>T (p.Gln1666Ter) rs1460626520 0.00001
NM_001004334.4(GPR179):c.5639A>G (p.Asp1880Gly) rs745835590 0.00001
NM_001004334.4(GPR179):c.6457G>A (p.Gly2153Arg) rs757565461 0.00001
NM_001004334.4(GPR179):c.6621C>T (p.Ser2207=) rs781391422 0.00001
NM_001004334.4(GPR179):c.6965C>T (p.Thr2322Ile) rs759484427 0.00001
NM_001004334.4(GPR179):c.858A>G (p.Pro286=) rs758285150 0.00001
NM_001004334.4(GPR179):c.952C>T (p.Arg318Cys) rs773004800 0.00001
NM_001004334.4(GPR179):c.98G>A (p.Arg33His) rs886052900 0.00001
NM_001004334.4(GPR179):c.*17G>C rs770311999
NM_001004334.4(GPR179):c.*388A>C rs1018088318
NM_001004334.4(GPR179):c.*516T>C rs886052893
NM_001004334.4(GPR179):c.*640G>T rs2037280359
NM_001004334.4(GPR179):c.1294C>A (p.Pro432Thr) rs772895584
NM_001004334.4(GPR179):c.134G>T (p.Gly45Val) rs886052899
NM_001004334.4(GPR179):c.1388T>A (p.Ile463Asn) rs886052897
NM_001004334.4(GPR179):c.1477C>A (p.His493Asn) rs114716738
NM_001004334.4(GPR179):c.1784+9G>A rs774545222
NM_001004334.4(GPR179):c.1916G>A (p.Arg639Gln) rs62073369
NM_001004334.4(GPR179):c.2002T>C (p.Trp668Arg) rs2037374851
NM_001004334.4(GPR179):c.2413G>C (p.Glu805Gln) rs199619898
NM_001004334.4(GPR179):c.2419G>A (p.Val807Met) rs2037354573
NM_001004334.4(GPR179):c.2556C>T (p.Leu852=) rs777488974
NM_001004334.4(GPR179):c.278dup (p.Ser94fs) rs794726685
NM_001004334.4(GPR179):c.3092G>A (p.Arg1031Lys)
NM_001004334.4(GPR179):c.3125C>G (p.Ala1042Gly) rs886052896
NM_001004334.4(GPR179):c.3364_3365del (p.Ser1122fs) rs1205982736
NM_001004334.4(GPR179):c.3451G>A (p.Glu1151Lys) rs1170813264
NM_001004334.4(GPR179):c.3460C>T (p.Gln1154Ter) rs757044884
NM_001004334.4(GPR179):c.3474C>A (p.Asn1158Lys) rs755044433
NM_001004334.4(GPR179):c.3518G>C (p.Ser1173Thr) rs565610587
NM_001004334.4(GPR179):c.3699G>T (p.Leu1233=) rs35803744
NM_001004334.4(GPR179):c.3846C>T (p.Asp1282=) rs2037332515
NM_001004334.4(GPR179):c.3876G>A (p.Glu1292=) rs1699475935
NM_001004334.4(GPR179):c.3919C>T (p.Arg1307Trp) rs765046358
NM_001004334.4(GPR179):c.4073T>G (p.Val1358Gly) rs752363198
NM_001004334.4(GPR179):c.4081C>G (p.Pro1361Ala) rs1471292987
NM_001004334.4(GPR179):c.4888G>A (p.Glu1630Lys) rs149998444
NM_001004334.4(GPR179):c.5119T>C (p.Trp1707Arg) rs769294419
NM_001004334.4(GPR179):c.5386T>G (p.Cys1796Gly) rs369190209
NM_001004334.4(GPR179):c.5769T>C (p.Gly1923=) rs2037304044
NM_001004334.4(GPR179):c.6012T>A (p.Asp2004Glu) rs886052895
NM_001004334.4(GPR179):c.6169G>A (p.Val2057Met) rs762962801
NM_001004334.4(GPR179):c.984del (p.Ser329fs) rs770066665

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.