ClinVar Miner

List of variants in gene DOCK7 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_001367561.1(DOCK7):c.1047C>T (p.Val349=) rs139793443 0.00290
NM_001367561.1(DOCK7):c.4668G>A (p.Arg1556=) rs115353638 0.00107
NM_001367561.1(DOCK7):c.480T>C (p.Ser160=) rs142535471 0.00083
NM_001367561.1(DOCK7):c.2605G>A (p.Gly869Ser) rs201823761 0.00069
NM_001367561.1(DOCK7):c.4368G>A (p.Glu1456=) rs149367921 0.00036
NM_001367561.1(DOCK7):c.1872-6A>T rs756259590 0.00033
NM_001367561.1(DOCK7):c.1265T>C (p.Val422Ala) rs199708701 0.00029
NM_001367561.1(DOCK7):c.6018G>A (p.Glu2006=) rs143414077 0.00029
NM_001367561.1(DOCK7):c.156C>T (p.Thr52=) rs147045113 0.00025
NM_001367561.1(DOCK7):c.4653T>C (p.Ala1551=) rs150922364 0.00021
NM_001367561.1(DOCK7):c.6045C>T (p.Pro2015=) rs202231787 0.00019
NM_001367561.1(DOCK7):c.2578C>A (p.Pro860Thr) rs150032045 0.00016
NM_001367561.1(DOCK7):c.3717C>G (p.Ala1239=) rs375372678 0.00016
NM_001367561.1(DOCK7):c.4491G>A (p.Thr1497=) rs373928701 0.00016
NM_001367561.1(DOCK7):c.5208A>T (p.Val1736=) rs144604663 0.00016
NM_001367561.1(DOCK7):c.4056A>G (p.Ser1352=) rs144949335 0.00011
NM_001367561.1(DOCK7):c.5463T>A (p.Leu1821=) rs201081054 0.00006
NM_001367561.1(DOCK7):c.692G>A (p.Arg231His) rs757667036 0.00006
NM_001367561.1(DOCK7):c.2630C>G (p.Ala877Gly) rs139050582 0.00004
NM_001367561.1(DOCK7):c.2250C>T (p.His750=) rs201252647 0.00003
NM_001367561.1(DOCK7):c.3152C>T (p.Thr1051Met) rs757960377 0.00003
NM_001367561.1(DOCK7):c.3211A>G (p.Asn1071Asp) rs371894094 0.00003
NM_001367561.1(DOCK7):c.72C>T (p.Ser24=) rs369563931 0.00003
NM_001367561.1(DOCK7):c.1182T>C (p.Tyr394=) rs768933704 0.00001
NM_001367561.1(DOCK7):c.1293G>T (p.Gly431=) rs777222905 0.00001
NM_001367561.1(DOCK7):c.1884T>G (p.Phe628Leu) rs1188863501 0.00001
NM_001367561.1(DOCK7):c.258T>C (p.Asp86=) rs767000347 0.00001
NM_001367561.1(DOCK7):c.3761C>T (p.Pro1254Leu) rs1427395524 0.00001
NM_001367561.1(DOCK7):c.5359A>G (p.Met1787Val) rs775189099 0.00001
NM_001367561.1(DOCK7):c.5796C>T (p.Phe1932=) rs771762947 0.00001
NM_001367561.1(DOCK7):c.5810A>G (p.Asn1937Ser) rs764578433 0.00001
NM_001367561.1(DOCK7):c.1410A>C (p.Thr470=)
NM_001367561.1(DOCK7):c.1502G>A (p.Arg501Gln)
NM_001367561.1(DOCK7):c.171A>C (p.Pro57=)
NM_001367561.1(DOCK7):c.1801-1565T>C
NM_001367561.1(DOCK7):c.1801-1593_1801-1590del rs1571649028
NM_001367561.1(DOCK7):c.1872-6del rs1161370391
NM_001367561.1(DOCK7):c.1900G>C (p.Val634Leu) rs774732062
NM_001367561.1(DOCK7):c.1985C>T (p.Pro662Leu) rs1417203749
NM_001367561.1(DOCK7):c.3060G>A (p.Val1020=)
NM_001367561.1(DOCK7):c.3114A>G (p.Pro1038=)
NM_001367561.1(DOCK7):c.3486T>G (p.Ser1162=)
NM_001367561.1(DOCK7):c.3852_3854del (p.Met1284del) rs751833296
NM_001367561.1(DOCK7):c.5049del (p.Pro1684fs) rs1064797112
NM_001367561.1(DOCK7):c.5064G>A (p.Leu1688=) rs2149298969
NM_001367561.1(DOCK7):c.5418del (p.Ala1807fs) rs1646379664
NM_001367561.1(DOCK7):c.5634+1G>A rs1646006817
NM_001367561.1(DOCK7):c.5731A>G (p.Ile1911Val) rs1645957860
NM_001367561.1(DOCK7):c.5829C>T (p.Tyr1943=)
NM_001367561.1(DOCK7):c.6108G>A (p.Gly2036=)
NM_001367561.1(DOCK7):c.6381-6dup rs773882812

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