ClinVar Miner

List of variants in gene DCAF17 reported as benign for Woodhouse-Sakati syndrome

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP
NM_025000.4(DCAF17):c.*1005A>G rs73976168
NM_025000.4(DCAF17):c.*1034G>A
NM_025000.4(DCAF17):c.*1521A>G
NM_025000.4(DCAF17):c.*1565del rs560178345
NM_025000.4(DCAF17):c.*188T>A rs142315519
NM_025000.4(DCAF17):c.*1965A>G
NM_025000.4(DCAF17):c.*2183C>G rs73976170
NM_025000.4(DCAF17):c.*2340C>T rs888428
NM_025000.4(DCAF17):c.*2348G>A rs112519318
NM_025000.4(DCAF17):c.*2425T>A rs12151641
NM_025000.4(DCAF17):c.*2473G>A rs57999878
NM_025000.4(DCAF17):c.*2775G>T rs16859404
NM_025000.4(DCAF17):c.*2795T>C rs17221346
NM_025000.4(DCAF17):c.*3112C>G rs17221367
NM_025000.4(DCAF17):c.*350G>A rs3795996
NM_025000.4(DCAF17):c.*3703A>G rs9789572
NM_025000.4(DCAF17):c.*3712A>G rs74780004
NM_025000.4(DCAF17):c.*378T>C
NM_025000.4(DCAF17):c.*3829G>A rs59827170
NM_025000.4(DCAF17):c.*570G>A rs3795998
NM_025000.4(DCAF17):c.*676T>G rs3821084
NM_025000.4(DCAF17):c.1267-7C>T rs3731981
NM_025000.4(DCAF17):c.127-15C>A rs146556466
NM_025000.4(DCAF17):c.1320T>C (p.Ala440=) rs3731980
NM_025000.4(DCAF17):c.150C>T (p.Val50=) rs6751956
NM_025000.4(DCAF17):c.322-14C>T rs192861143
NM_025000.4(DCAF17):c.555T>A (p.His185Gln) rs3731984
NM_025000.4(DCAF17):c.732+70dup
NM_025000.4(DCAF17):c.939G>A (p.Gln313=) rs61731491
NM_025000.4(DCAF17):c.999A>G (p.Gln333=) rs3731983

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