ClinVar Miner

List of variants in gene ADGRV1 reported as pathogenic for not provided

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Gene type:
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Total variants: 19
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HGVS dbSNP
GRCh37/hg19 5q14.3(chr5:89940237-89999954)x1
GRCh37/hg19 5q14.3(chr5:90112102-90219415)x1
NM_032119.4(ADGRV1):c.10213C>T (p.Arg3405Ter) rs763670293
NM_032119.4(ADGRV1):c.10736_10737del (p.Ala3579fs) rs1307312865
NM_032119.4(ADGRV1):c.11122-2A>G rs1057517741
NM_032119.4(ADGRV1):c.11410C>T (p.Arg3804Ter) rs767570081
NM_032119.4(ADGRV1):c.12197_12209delinsTGGGA (p.Gly4066fs) rs1554107590
NM_032119.4(ADGRV1):c.12368dup (p.Ser4124fs) rs1561701900
NM_032119.4(ADGRV1):c.12823C>T (p.Gln4275Ter) rs768589991
NM_032119.4(ADGRV1):c.15984del (p.Tyr5329fs) rs1554125179
NM_032119.4(ADGRV1):c.17062C>T (p.Arg5688Ter) rs747622607
NM_032119.4(ADGRV1):c.17314C>T (p.Arg5772Ter) rs749956288
NM_032119.4(ADGRV1):c.17668_17669del (p.Met5890fs) rs757696771
NM_032119.4(ADGRV1):c.4251del (p.Lys1417fs) rs1554072688
NM_032119.4(ADGRV1):c.4702del (p.Ser1568fs) rs794727347
NM_032119.4(ADGRV1):c.627del (p.Gly210fs) rs1554063934
NM_032119.4(ADGRV1):c.6901C>T (p.Gln2301Ter) rs121909762
NM_032119.4(ADGRV1):c.8204del (p.Asn2735fs) rs794727584
NM_032119.4(ADGRV1):c.956dup (p.Asn319fs) rs752179149

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