ClinVar Miner

List of variants in gene ADGRV1 reported as likely benign by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP
NM_032119.3(ADGRV1):c.18433-7_18433-5delTTT rs35858094
NM_032119.3(ADGRV1):c.8730+10dupT rs60522638
NM_032119.4(ADGRV1):c.11201T>C (p.Val3734Ala) rs113498662
NM_032119.4(ADGRV1):c.1131T>G (p.Ser377=) rs200435877
NM_032119.4(ADGRV1):c.11568T>C (p.Val3856=) rs143004930
NM_032119.4(ADGRV1):c.11805C>T (p.Asn3935=) rs144269892
NM_032119.4(ADGRV1):c.12269C>A (p.Thr4090Asn) rs199839743
NM_032119.4(ADGRV1):c.12527+6G>T rs141701016
NM_032119.4(ADGRV1):c.14223C>T (p.Ala4741=)
NM_032119.4(ADGRV1):c.14943G>C (p.Gln4981His) rs200153555
NM_032119.4(ADGRV1):c.1522A>C (p.Ile508Leu) rs61744480
NM_032119.4(ADGRV1):c.15669G>A (p.Gly5223=)
NM_032119.4(ADGRV1):c.18433-5dup rs35858094
NM_032119.4(ADGRV1):c.18746T>G (p.Leu6249Arg) rs41311625
NM_032119.4(ADGRV1):c.18804T>G (p.Gly6268=) rs200075846
NM_032119.4(ADGRV1):c.2119A>T (p.Ile707Leu) rs200897149
NM_032119.4(ADGRV1):c.22+9T>C rs368604803
NM_032119.4(ADGRV1):c.2456G>A (p.Ser819Asn) rs182395524
NM_032119.4(ADGRV1):c.3151G>T (p.Asp1051Tyr) rs145556097
NM_032119.4(ADGRV1):c.3191A>C (p.Glu1064Ala) rs190922596
NM_032119.4(ADGRV1):c.3255T>C (p.Asp1085=) rs183447491
NM_032119.4(ADGRV1):c.463A>G (p.Ile155Val) rs199873924
NM_032119.4(ADGRV1):c.7176C>T (p.Ser2392=) rs111033452
NM_032119.4(ADGRV1):c.7874G>A (p.Arg2625His) rs201214794
NM_032119.4(ADGRV1):c.8088G>A (p.Leu2696=) rs373069459
NM_032119.4(ADGRV1):c.8172C>T (p.Phe2724=) rs371019516
NM_032119.4(ADGRV1):c.8691A>C (p.Glu2897Asp) rs201586455
NM_032119.4(ADGRV1):c.8730+10_8730+11insC rs377585302

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