ClinVar Miner

List of variants in gene DCAF17 studied for Woodhouse-Sakati syndrome

Included ClinVar conditions (1):
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Gene type:
ClinVar version:
Total variants: 125
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HGVS dbSNP
NC_000002.12:g.171485060G>A
NM_025000.4(DCAF17):c.*1005A>G rs73976168
NM_025000.4(DCAF17):c.*1034G>A
NM_025000.4(DCAF17):c.*105A>G rs551802113
NM_025000.4(DCAF17):c.*1120A>T
NM_025000.4(DCAF17):c.*1124G>A
NM_025000.4(DCAF17):c.*1165C>G rs886055109
NM_025000.4(DCAF17):c.*1258dup rs745661005
NM_025000.4(DCAF17):c.*126A>T rs139116642
NM_025000.4(DCAF17):c.*1370C>T
NM_025000.4(DCAF17):c.*1485_*1486AG[1] rs886055111
NM_025000.4(DCAF17):c.*1521A>G
NM_025000.4(DCAF17):c.*1531T>C rs537066061
NM_025000.4(DCAF17):c.*153C>G
NM_025000.4(DCAF17):c.*1540C>T
NM_025000.4(DCAF17):c.*1557T>A
NM_025000.4(DCAF17):c.*1565del rs560178345
NM_025000.4(DCAF17):c.*15T>C rs146258833
NM_025000.4(DCAF17):c.*1692G>C
NM_025000.4(DCAF17):c.*1747C>A rs747014569
NM_025000.4(DCAF17):c.*1841G>T rs114519296
NM_025000.4(DCAF17):c.*188T>A rs142315519
NM_025000.4(DCAF17):c.*1965A>G
NM_025000.4(DCAF17):c.*2066A>G rs886055113
NM_025000.4(DCAF17):c.*2113C>A
NM_025000.4(DCAF17):c.*211C>A
NM_025000.4(DCAF17):c.*2183C>G rs73976170
NM_025000.4(DCAF17):c.*2202A>G rs886055114
NM_025000.4(DCAF17):c.*2241T>C
NM_025000.4(DCAF17):c.*2292G>A rs373833929
NM_025000.4(DCAF17):c.*2303G>A
NM_025000.4(DCAF17):c.*2312G>A rs777311799
NM_025000.4(DCAF17):c.*2318C>T
NM_025000.4(DCAF17):c.*2340C>T rs888428
NM_025000.4(DCAF17):c.*2348G>A rs112519318
NM_025000.4(DCAF17):c.*2380A>G rs553179661
NM_025000.4(DCAF17):c.*2425T>A rs12151641
NM_025000.4(DCAF17):c.*2429A>G rs778932293
NM_025000.4(DCAF17):c.*2473G>A rs57999878
NM_025000.4(DCAF17):c.*2535C>A
NM_025000.4(DCAF17):c.*2591A>G
NM_025000.4(DCAF17):c.*2623T>G rs886055115
NM_025000.4(DCAF17):c.*2747C>T rs886055116
NM_025000.4(DCAF17):c.*2775G>T rs16859404
NM_025000.4(DCAF17):c.*2795T>C rs17221346
NM_025000.4(DCAF17):c.*2943C>T
NM_025000.4(DCAF17):c.*2947A>C
NM_025000.4(DCAF17):c.*2965_*2967TTC[3] rs886055117
NM_025000.4(DCAF17):c.*2971A>G rs576169953
NM_025000.4(DCAF17):c.*2976A>G rs78561668
NM_025000.4(DCAF17):c.*3008_*3011TTGT[1] rs374810983
NM_025000.4(DCAF17):c.*3022A>G
NM_025000.4(DCAF17):c.*3107A>G
NM_025000.4(DCAF17):c.*3112C>G rs17221367
NM_025000.4(DCAF17):c.*3170A>G
NM_025000.4(DCAF17):c.*3453A>G rs747674263
NM_025000.4(DCAF17):c.*350G>A rs3795996
NM_025000.4(DCAF17):c.*3551C>T
NM_025000.4(DCAF17):c.*3703A>G rs9789572
NM_025000.4(DCAF17):c.*3705A>G rs577520268
NM_025000.4(DCAF17):c.*3712A>G rs74780004
NM_025000.4(DCAF17):c.*378T>C
NM_025000.4(DCAF17):c.*3811A>G
NM_025000.4(DCAF17):c.*3829G>A rs59827170
NM_025000.4(DCAF17):c.*3835A>G rs886055119
NM_025000.4(DCAF17):c.*3880G>T rs754667938
NM_025000.4(DCAF17):c.*423T>C
NM_025000.4(DCAF17):c.*432C>G
NM_025000.4(DCAF17):c.*48A>T rs753380867
NM_025000.4(DCAF17):c.*530A>G rs115676571
NM_025000.4(DCAF17):c.*570G>A rs3795998
NM_025000.4(DCAF17):c.*676T>G rs3821084
NM_025000.4(DCAF17):c.*677C>A rs115798465
NM_025000.4(DCAF17):c.*808T>A rs886055108
NM_025000.4(DCAF17):c.*864A>G
NM_025000.4(DCAF17):c.*876G>C
NM_025000.4(DCAF17):c.*926G>T
NM_025000.4(DCAF17):c.1030T>C (p.Trp344Arg) rs78488864
NM_025000.4(DCAF17):c.1083T>C (p.Asn361=) rs193214847
NM_025000.4(DCAF17):c.1091+13A>G rs886055107
NM_025000.4(DCAF17):c.1091+6T>G rs1559289651
NM_025000.4(DCAF17):c.1266+4T>C
NM_025000.4(DCAF17):c.1266+6G>A rs557741620
NM_025000.4(DCAF17):c.1267-7C>T rs3731981
NM_025000.4(DCAF17):c.127-15C>A rs146556466
NM_025000.4(DCAF17):c.127-3_127-1delinsAA rs1574303761
NM_025000.4(DCAF17):c.1320T>C (p.Ala440=) rs3731980
NM_025000.4(DCAF17):c.133A>G (p.Thr45Ala)
NM_025000.4(DCAF17):c.137A>T (p.Lys46Ile) rs375426959
NM_025000.4(DCAF17):c.1422+14G>A
NM_025000.4(DCAF17):c.1422+5G>T rs1314048356
NM_025000.4(DCAF17):c.1426T>C (p.Tyr476His) rs142735693
NM_025000.4(DCAF17):c.150C>T (p.Val50=) rs6751956
NM_025000.4(DCAF17):c.1519T>C (p.Cys507Arg) rs147685213
NM_025000.4(DCAF17):c.181T>C (p.Tyr61His)
NM_025000.4(DCAF17):c.184G>A (p.Glu62Lys) rs201346228
NM_025000.4(DCAF17):c.192A>G (p.Gly64=) rs200189652
NM_025000.4(DCAF17):c.209A>G (p.Asn70Ser) rs200380164
NM_025000.4(DCAF17):c.214C>T (p.Arg72Trp) rs886055106
NM_025000.4(DCAF17):c.230+15A>G rs778241115
NM_025000.4(DCAF17):c.270del (p.Lys90fs) rs879253799
NM_025000.4(DCAF17):c.270dup (p.Cys91fs) rs879253799
NM_025000.4(DCAF17):c.289dup (p.Ile97fs) rs863224865
NM_025000.4(DCAF17):c.322-14C>T rs192861143
NM_025000.4(DCAF17):c.341C>A (p.Ser114Ter) rs760978794
NM_025000.4(DCAF17):c.387G>A (p.Trp129Ter) rs1559264135
NM_025000.4(DCAF17):c.436del (p.Ala147fs) rs797045038
NM_025000.4(DCAF17):c.532C>T (p.Arg178Trp) rs377364475
NM_025000.4(DCAF17):c.533G>A (p.Arg178Gln) rs202231211
NM_025000.4(DCAF17):c.555T>A (p.His185Gln) rs3731984
NM_025000.4(DCAF17):c.579C>A (p.Phe193Leu) rs150095386
NM_025000.4(DCAF17):c.580C>T (p.Arg194Ter) rs1470826074
NM_025000.4(DCAF17):c.581G>A (p.Arg194Gln) rs371230892
NM_025000.4(DCAF17):c.605G>A (p.Gly202Glu)
NM_025000.4(DCAF17):c.724G>A (p.Ala242Thr) rs149650431
NM_025000.4(DCAF17):c.732+70dup rs58636477
NM_025000.4(DCAF17):c.735C>G (p.Phe245Leu) rs773360559
NM_025000.4(DCAF17):c.792T>C (p.Thr264=) rs199742600
NM_025000.4(DCAF17):c.906G>A (p.Trp302Ter) rs761229686
NM_025000.4(DCAF17):c.913A>G (p.Ile305Val) rs114419034
NM_025000.4(DCAF17):c.939G>A (p.Gln313=) rs61731491
NM_025000.4(DCAF17):c.959G>T (p.Cys320Phe)
NM_025000.4(DCAF17):c.982-2A>C rs780493577
NM_025000.4(DCAF17):c.986A>C (p.Lys329Thr)
NM_025000.4(DCAF17):c.999A>G (p.Gln333=) rs3731983

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