ClinVar Miner

List of variants in gene ARHGAP31 reported as uncertain significance for Adams-Oliver syndrome

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NM_020754.3(ARHGAP31):c.*1089C>T rs886057805
NM_020754.3(ARHGAP31):c.*1186A>G rs886057806
NM_020754.3(ARHGAP31):c.*1233A>G rs886057807
NM_020754.3(ARHGAP31):c.*1373G>A rs750355275
NM_020754.3(ARHGAP31):c.*1648C>T rs886057809
NM_020754.3(ARHGAP31):c.*1811G>A rs886057810
NM_020754.3(ARHGAP31):c.*183A>G rs886057804
NM_020754.3(ARHGAP31):c.*1978T>A rs886057811
NM_020754.3(ARHGAP31):c.*2101A>T rs886057812
NM_020754.3(ARHGAP31):c.*2110G>A rs886057813
NM_020754.3(ARHGAP31):c.*2178C>T rs770268525
NM_020754.3(ARHGAP31):c.*2471G>T rs886057814
NM_020754.3(ARHGAP31):c.*2743C>G rs78013508
NM_020754.3(ARHGAP31):c.*2764C>A rs886057815
NM_020754.3(ARHGAP31):c.*2912A>G rs886057816
NM_020754.3(ARHGAP31):c.*2935C>T rs886057817
NM_020754.3(ARHGAP31):c.*38T>G rs886057803
NM_020754.3(ARHGAP31):c.*610T>A rs779853850
NM_020754.3(ARHGAP31):c.*737A>G rs185158937
NM_020754.3(ARHGAP31):c.-105C>T rs886057797
NM_020754.3(ARHGAP31):c.-165_-159dup rs886057796
NM_020754.3(ARHGAP31):c.-199C>T rs886057795
NM_020754.3(ARHGAP31):c.-209C>T rs886057794
NM_020754.3(ARHGAP31):c.-390G>C rs886057793
NM_020754.3(ARHGAP31):c.-443C>G rs886057792
NM_020754.3(ARHGAP31):c.1044C>T (p.Asp348=) rs369521143
NM_020754.3(ARHGAP31):c.1184A>G (p.Glu395Gly) rs760929413
NM_020754.3(ARHGAP31):c.1307G>A (p.Arg436Gln) rs752035106
NM_020754.3(ARHGAP31):c.1371G>T (p.Ser457=) rs753753846
NM_020754.3(ARHGAP31):c.1538C>T (p.Pro513Leu) rs886057800
NM_020754.3(ARHGAP31):c.1823C>T (p.Pro608Leu) rs773084870
NM_020754.3(ARHGAP31):c.2359C>T (p.Pro787Ser) rs186621177
NM_020754.3(ARHGAP31):c.2412G>A (p.Pro804=) rs776194035
NM_020754.3(ARHGAP31):c.2497C>T (p.Leu833Phe) rs201970872
NM_020754.3(ARHGAP31):c.2568G>A (p.Gly856=) rs770529130
NM_020754.3(ARHGAP31):c.2777C>T (p.Ala926Val) rs771980065
NM_020754.3(ARHGAP31):c.2940A>G (p.Thr980=) rs746965144
NM_020754.3(ARHGAP31):c.3179G>A (p.Gly1060Asp) rs886057801
NM_020754.3(ARHGAP31):c.349-9_349-7del rs771235886
NM_020754.3(ARHGAP31):c.3876A>G (p.Pro1292=) rs886057802
NM_020754.3(ARHGAP31):c.4084C>G (p.Pro1362Ala) rs376066861
NM_020754.3(ARHGAP31):c.436T>C (p.Leu146=) rs758994452
NM_020754.3(ARHGAP31):c.473C>T (p.Ser158Phe) rs779651681
NM_020754.3(ARHGAP31):c.843C>T (p.Gly281=) rs886057799
NM_020754.3(ARHGAP31):c.848T>A (p.Leu283His) rs773314411

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