ClinVar Miner

List of variants in gene ADGRV1 reported as benign for Usher syndrome type 2

Included ClinVar conditions (9):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
Download table as spreadsheet
HGVS dbSNP
NM_032119.4(ADGRV1):c.*60A>G
NM_032119.4(ADGRV1):c.-47G>C rs116110048
NM_032119.4(ADGRV1):c.-98G>A rs7706355
NM_032119.4(ADGRV1):c.10039T>C (p.Phe3347Leu) rs10067636
NM_032119.4(ADGRV1):c.10411G>A (p.Glu3471Lys) rs2366928
NM_032119.4(ADGRV1):c.10872A>G (p.Gln3624=) rs17624033
NM_032119.4(ADGRV1):c.11472G>A (p.Leu3824=) rs74327115
NM_032119.4(ADGRV1):c.11481T>C (p.Asp3827=) rs16869083
NM_032119.4(ADGRV1):c.11599G>A (p.Glu3867Lys) rs10062026
NM_032119.4(ADGRV1):c.11682C>T (p.Pro3894=) rs2438349
NM_032119.4(ADGRV1):c.12592G>A (p.Val4198Met) rs2460169
NM_032119.4(ADGRV1):c.12927G>A (p.Ala4309=) rs35092519
NM_032119.4(ADGRV1):c.13599A>G (p.Thr4533=) rs17554631
NM_032119.4(ADGRV1):c.14029T>C (p.Phe4677Leu) rs62000408
NM_032119.4(ADGRV1):c.14319A>G (p.Ile4773Met)
NM_032119.4(ADGRV1):c.14654A>G (p.Asn4885Ser) rs61731030
NM_032119.4(ADGRV1):c.14905T>C (p.Trp4969Arg) rs7729495
NM_032119.4(ADGRV1):c.16031A>G (p.Glu5344Gly) rs2438374
NM_032119.4(ADGRV1):c.16164A>G (p.Arg5388=) rs41304884
NM_032119.4(ADGRV1):c.16248C>T (p.Val5416=) rs3763073
NM_032119.4(ADGRV1):c.16279G>A (p.Val5427Met) rs2438378
NM_032119.4(ADGRV1):c.16377G>T (p.Gln5459His) rs371947306
NM_032119.4(ADGRV1):c.1652T>C (p.Val551Ala) rs6889939
NM_032119.4(ADGRV1):c.16949C>G (p.Thr5650Ser) rs61748627
NM_032119.4(ADGRV1):c.17626G>A (p.Val5876Ile) rs2247870
NM_032119.4(ADGRV1):c.1797A>T (p.Arg599Ser) rs200058876
NM_032119.4(ADGRV1):c.18475A>G (p.Met6159Val) rs77469944
NM_032119.4(ADGRV1):c.18625-7T>C rs7726023
NM_032119.4(ADGRV1):c.18741G>A (p.Gly6247=) rs13158963
NM_032119.4(ADGRV1):c.2001T>C (p.Asp667=) rs9293547
NM_032119.4(ADGRV1):c.2367+8C>T rs2366773
NM_032119.4(ADGRV1):c.2735-10C>A rs78625945
NM_032119.4(ADGRV1):c.3141A>G (p.Ala1047=) rs950692
NM_032119.4(ADGRV1):c.3279G>T (p.Leu1093Phe) rs2366777
NM_032119.4(ADGRV1):c.327C>T (p.Asp109=) rs61753944
NM_032119.4(ADGRV1):c.380T>G (p.Leu127Arg) rs41311333
NM_032119.4(ADGRV1):c.4506C>T (p.Pro1502=) rs17543819
NM_032119.4(ADGRV1):c.5346A>G (p.Gly1782=) rs10067298
NM_032119.4(ADGRV1):c.5747C>T (p.Thr1916Ile) rs35791889
NM_032119.4(ADGRV1):c.5780C>T (p.Thr1927Met) rs17544552
NM_032119.4(ADGRV1):c.581C>A (p.Pro194His) rs61745498
NM_032119.4(ADGRV1):c.5830G>A (p.Asp1944Asn) rs41302834
NM_032119.4(ADGRV1):c.5851G>A (p.Val1951Ile) rs4916684
NM_032119.4(ADGRV1):c.5953A>G (p.Asn1985Asp) rs41303352
NM_032119.4(ADGRV1):c.5960C>T (p.Pro1987Leu) rs4916685
NM_032119.4(ADGRV1):c.6012G>T (p.Leu2004Phe) rs16868972
NM_032119.4(ADGRV1):c.6133G>A (p.Gly2045Arg) rs41308846
NM_032119.4(ADGRV1):c.6289C>T (p.Arg2097Cys) rs16868974
NM_032119.4(ADGRV1):c.6559A>G (p.Ile2187Val) rs200512504
NM_032119.4(ADGRV1):c.6695A>G (p.Tyr2232Cys) rs10037067
NM_032119.4(ADGRV1):c.6952-10G>A rs10040165
NM_032119.4(ADGRV1):c.7034A>G (p.Asn2345Ser) rs2366926
NM_032119.4(ADGRV1):c.7206G>A (p.Glu2402=) rs16876822
NM_032119.4(ADGRV1):c.7229A>G (p.Tyr2410Cys) rs111033430
NM_032119.4(ADGRV1):c.7293C>T (p.Ala2431=) rs77791584
NM_032119.4(ADGRV1):c.7576A>G (p.Ile2526Val) rs75191159
NM_032119.4(ADGRV1):c.7751A>G (p.Asn2584Ser) rs1878878
NM_032119.4(ADGRV1):c.7813T>G (p.Leu2605Val) rs79915053
NM_032119.4(ADGRV1):c.7945+6C>T rs139278305
NM_032119.4(ADGRV1):c.8291C>T (p.Ser2764Leu) rs16869016
NM_032119.4(ADGRV1):c.8538T>G (p.Leu2846=) rs6880570
NM_032119.4(ADGRV1):c.8876G>A (p.Arg2959Gln) rs73175207
NM_032119.4(ADGRV1):c.9280G>A (p.Val3094Ile) rs13157270
NM_032119.4(ADGRV1):c.9366A>G (p.Thr3122=) rs200412477
NM_032119.4(ADGRV1):c.9743G>A (p.Gly3248Asp) rs16869032
NM_032119.4(ADGRV1):c.9771C>T (p.Ser3257=) rs16869039
NM_032119.4(ADGRV1):c.9927T>G (p.Pro3309=) rs16869042

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.