ClinVar Miner

List of variants in gene ADGRV1 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_032119.4(ADGRV1):c.6317C>T (p.Ala2106Val) rs186999408 0.00271
NM_032119.4(ADGRV1):c.12212G>A (p.Arg4071Gln) rs202190568 0.00074
NM_032119.4(ADGRV1):c.1849G>A (p.Val617Met) rs199988872 0.00046
NM_032119.4(ADGRV1):c.16331C>A (p.Thr5444Lys) rs370906851 0.00039
NM_032119.4(ADGRV1):c.1718G>T (p.Gly573Val) rs200789563 0.00036
NM_032119.4(ADGRV1):c.9440G>A (p.Arg3147Gln) rs200792658 0.00036
NM_032119.4(ADGRV1):c.4507G>A (p.Ala1503Thr) rs201391886 0.00034
NM_032119.4(ADGRV1):c.6994A>T (p.Ile2332Phe) rs193030567 0.00019
NM_032119.4(ADGRV1):c.2636C>T (p.Thr879Met) rs201007778 0.00014
NM_032119.4(ADGRV1):c.3974C>T (p.Thr1325Met) rs756414393 0.00007
NM_032119.4(ADGRV1):c.4786G>A (p.Val1596Ile) rs371179945 0.00005
NM_032119.4(ADGRV1):c.18831A>G (p.Glu6277=) rs549421635 0.00004
NM_032119.4(ADGRV1):c.2660A>G (p.His887Arg) rs560889543 0.00004
NM_032119.4(ADGRV1):c.17621A>G (p.Lys5874Arg) rs199516167 0.00003
NM_032119.4(ADGRV1):c.10142A>G (p.Asp3381Gly) rs768784845 0.00002
NM_032119.4(ADGRV1):c.442T>C (p.Ser148Pro) rs769994130 0.00002
NM_032119.4(ADGRV1):c.13653+6T>C rs781455871 0.00001
NM_032119.4(ADGRV1):c.137C>T (p.Thr46Ile) rs754162988 0.00001
NM_032119.4(ADGRV1):c.5560A>G (p.Ile1854Val) rs758419783 0.00001
NM_032119.4(ADGRV1):c.7718A>G (p.Asn2573Ser) rs1268883829 0.00001
NM_032119.4(ADGRV1):c.8791A>G (p.Met2931Val) rs1250073917 0.00001
NM_032119.4(ADGRV1):c.9940G>A (p.Ala3314Thr) rs773086150 0.00001
NM_032119.4(ADGRV1):c.10309T>C (p.Trp3437Arg) rs2149813290
NM_032119.4(ADGRV1):c.10939A>C (p.Asn3647His)
NM_032119.4(ADGRV1):c.11692A>G (p.Ile3898Val)
NM_032119.4(ADGRV1):c.12125T>C (p.Met4042Thr) rs778537428
NM_032119.4(ADGRV1):c.12456del (p.Gly4152_Ile4153insTer)
NM_032119.4(ADGRV1):c.13964C>T (p.Ser4655Leu)
NM_032119.4(ADGRV1):c.15301G>A (p.Gly5101Arg)
NM_032119.4(ADGRV1):c.16658C>A (p.Ala5553Asp) rs1554133453
NM_032119.4(ADGRV1):c.296C>T (p.Ala99Val) rs1763569691
NM_032119.4(ADGRV1):c.361C>A (p.Pro121Thr)
NM_032119.4(ADGRV1):c.4036C>A (p.Pro1346Thr)
NM_032119.4(ADGRV1):c.454-3T>C
NM_032119.4(ADGRV1):c.8050A>G (p.Ile2684Val) rs1580775969

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