ClinVar Miner

List of variants in gene DOCK7 reported as benign for central nervous system disorder

Included ClinVar conditions (2490):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_001367561.1(DOCK7):c.6212+19G>A rs1168007 0.96294
NM_001367561.1(DOCK7):c.5062T>C (p.Leu1688=) rs10889335 0.34717
NM_001367561.1(DOCK7):c.4283-4A>G rs17123688 0.03743
NM_001367561.1(DOCK7):c.6255G>A (p.Pro2085=) rs35747851 0.01994
NM_001367561.1(DOCK7):c.1389A>C (p.Arg463=) rs35627175 0.01901
NM_001367561.1(DOCK7):c.3472-5A>G rs76660788 0.01882
NM_001367561.1(DOCK7):c.2471T>C (p.Ile824Thr) rs35400360 0.01182
NM_001367561.1(DOCK7):c.1460A>G (p.Lys487Arg) rs72913293 0.01118
NM_001367561.1(DOCK7):c.4696G>A (p.Gly1566Ser) rs147103646 0.00601
NM_001367561.1(DOCK7):c.6381-19C>T rs146910328 0.00591
NM_001367561.1(DOCK7):c.1392A>G (p.Pro464=) rs116172511 0.00571
NM_001367561.1(DOCK7):c.2859+12A>G rs201742189 0.00297
NM_001367561.1(DOCK7):c.1047C>T (p.Val349=) rs139793443 0.00290
NM_001367561.1(DOCK7):c.2700C>T (p.Ser900=) rs35648144 0.00154
NM_001367561.1(DOCK7):c.2859+20T>C rs567794345 0.00124
NM_001367561.1(DOCK7):c.4668G>A (p.Arg1556=) rs115353638 0.00107
NM_001367561.1(DOCK7):c.4119+18C>T rs368702983 0.00083
NM_001367561.1(DOCK7):c.480T>C (p.Ser160=) rs142535471 0.00083
NM_001367561.1(DOCK7):c.2859+17dup rs559908969 0.00064
NM_001367561.1(DOCK7):c.4713C>T (p.His1571=) rs149949352 0.00058
NM_001367561.1(DOCK7):c.519+17T>G rs745941706 0.00032
NM_001367561.1(DOCK7):c.6045C>T (p.Pro2015=) rs202231787 0.00019
NM_001367561.1(DOCK7):c.3300+15G>A rs145276116 0.00011
NM_001367561.1(DOCK7):c.5724+18A>G rs377719435 0.00004
NM_001367561.1(DOCK7):c.2985T>A (p.Val995=) rs188467262 0.00003
NM_001367561.1(DOCK7):c.281G>A (p.Arg94Gln) rs570514826 0.00001
NM_001367561.1(DOCK7):c.1283-14del rs541344421
NM_001367561.1(DOCK7):c.1283-14dup rs541344421
NM_001367561.1(DOCK7):c.1520-17dup
NM_001367561.1(DOCK7):c.1872-9del rs199915737
NM_001367561.1(DOCK7):c.1872-9dup rs199915737
NM_001367561.1(DOCK7):c.3046-4dup rs574290909
NM_001367561.1(DOCK7):c.321-4del
NM_001367561.1(DOCK7):c.3781+15_3781+56del rs533117910
NM_001367561.1(DOCK7):c.541A>G (p.Met181Val) rs61743961
NM_001367561.1(DOCK7):c.5962-7del rs2149258818
NM_001367561.1(DOCK7):c.6381-6dup rs773882812
NM_001367561.1(DOCK7):c.819-11dup

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