"PreventionGenetics, part of Exact Sciences"[submitter] AND "DOCK6"[ge - ClinVar

Search results

Items: 94

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 787602	NM_020812.4(DOCK6):c.5976T>A (p.Ile1992=)	DOCK6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1376925	NM_020812.4(DOCK6):c.5912G>A (p.Arg1971Gln)	DOCK6 (R2006Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1303926	NM_020812.4(DOCK6):c.5832+5G>A	DOCK6	Single nucleotide variant (intron variant)	DOCK6-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 798660	NM_020812.4(DOCK6):c.5832+4C>T	DOCK6	Single nucleotide variant (intron variant)	DOCK6-related disorder +1 more	GBenign/Likely benign
Select item 724123	NM_020812.4(DOCK6):c.5700G>A (p.Thr1900=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GBenign/Likely benign
Select item 3033120	NM_020812.4(DOCK6):c.5688+10G>T	DOCK6	Single nucleotide variant (intron variant)	DOCK6-related disorder	GLikely benign
Select item 499271	NM_020812.4(DOCK6):c.5582G>A (p.Arg1861His)	DOCK6 (R1861H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3052569	NM_020812.4(DOCK6):c.5529C>T (p.Arg1843=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder	GLikely benign
Select item 2632233	NM_020812.4(DOCK6):c.5527C>T (p.Arg1843Cys)	DOCK6 (R1843C +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder	GUncertain significance
Select item 3061167	NM_020812.4(DOCK6):c.5466C>G (p.Ile1822Met)	DOCK6 (I1822M +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder	GUncertain significance
Select item 261358	NM_020812.4(DOCK6):c.5361+4C>T	DOCK6	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 3037399	NM_020812.4(DOCK6):c.5274C>A (p.Gly1758=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder	GLikely benign
Select item 1635910	NM_020812.4(DOCK6):c.5227G>A (p.Gly1743Ser)	DOCK6, DOCK6-AS1 (G1743S +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder +1 more	GLikely benign
Select item 597280	NM_020812.4(DOCK6):c.5088+8C>G	DOCK6, DOCK6-AS1	Single nucleotide variant (intron variant)	DOCK6-related disorder +2 more	GBenign/Likely benign
Select item 2081235	NM_020812.4(DOCK6):c.4986C>T (p.Asp1662=)	DOCK6, DOCK6-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2976666	NM_020812.4(DOCK6):c.4962G>A (p.Val1654=)	DOCK6, DOCK6-AS1	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GLikely benign
Select item 289212	NM_020812.4(DOCK6):c.4862T>C (p.Val1621Ala)	DOCK6, DOCK6-AS1 (V1621A +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 724923	NM_020812.4(DOCK6):c.4848C>T (p.Ala1616=)	DOCK6-AS1, DOCK6	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 261357	NM_020812.4(DOCK6):c.4548G>A (p.Thr1516=)	DOCK6, DOCK6-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 723457	NM_020812.4(DOCK6):c.4547C>T (p.Thr1516Met)	DOCK6, DOCK6-AS1 (T1551M +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder +2 more	GLikely benign
Select item 709958	NM_020812.4(DOCK6):c.4479C>T (p.Phe1493=)	DOCK6, DOCK6-AS1	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GBenign/Likely benign
Select item 202182	NM_020812.4(DOCK6):c.4469G>A (p.Arg1490Gln)	DOCK6, DOCK6-AS1 (R1490Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1601484	NM_020812.4(DOCK6):c.4446C>T (p.Ser1482=)	DOCK6, DOCK6-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3054531	NM_020812.4(DOCK6):c.4338+6C>T	DOCK6, DOCK6-AS1	Single nucleotide variant (intron variant)	DOCK6-related disorder	GLikely benign
Select item 740828	NM_020812.4(DOCK6):c.4218A>T (p.Ser1406=)	DOCK6, DOCK6-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 235741	NM_020812.4(DOCK6):c.4216T>G (p.Ser1406Ala)	DOCK6, DOCK6-AS1 (S1406A +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder +2 more	GUncertain significance
Select item 377033	NM_020812.4(DOCK6):c.4205C>T (p.Thr1402Met)	DOCK6, DOCK6-AS1 (T1402M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2054914	NM_020812.4(DOCK6):c.4204-3C>T	DOCK6, DOCK6-AS1	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 728625	NM_020812.4(DOCK6):c.4068C>T (p.Ser1356=)	DOCK6, DOCK6-AS1	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GLikely benign
Select item 2635901	NM_020812.4(DOCK6):c.3995G>C (p.Arg1332Pro)	DOCK6, DOCK6-AS1 (R1332P +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder	GUncertain significance
Select item 3046738	NM_020812.4(DOCK6):c.3933C>T (p.Phe1311=)	DOCK6, DOCK6-AS1	Single nucleotide variant (synonymous variant)	DOCK6-related disorder	GLikely benign
Select item 717084	NM_020812.4(DOCK6):c.3752G>A (p.Arg1251Gln)	DOCK6, DOCK6-AS1 (R1251Q +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 2629159	NM_020812.4(DOCK6):c.3719G>A (p.Arg1240His)	DOCK6, DOCK6-AS1 (R1240H +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder	GUncertain significance
Select item 499360	NM_020812.4(DOCK6):c.3562C>T (p.Gln1188Ter)	DOCK6, DOCK6-AS1 (Q1188* +1 more)	Single nucleotide variant (nonsense)	Adams-Oliver syndrome 1 +2 more	GPathogenic/Likely pathogenic
Select item 444446	NM_020812.4(DOCK6):c.3517C>T (p.Arg1173Trp)	DOCK6 (R1173W +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 722635	NM_020812.4(DOCK6):c.3486C>T (p.Ala1162=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GLikely benign
Select item 730994	NM_020812.4(DOCK6):c.3343A>G (p.Thr1115Ala)	DOCK6 (T1115A +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder +1 more	GLikely benign
Select item 734943	NM_020812.4(DOCK6):c.3264C>T (p.Ala1088=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GLikely benign
Select item 1206321	NM_020812.4(DOCK6):c.3190_3191del (p.Leu1064fs)	DOCK6 (L1064fs +1 more)	Deletion (frameshift variant)	Adams-Oliver syndrome 2 +2 more	GPathogenic
Select item 2445975	NM_020812.4(DOCK6):c.3180del (p.Cys1061fs)	DOCK6 (C1061fs +1 more)	Deletion (frameshift variant)	Adams-Oliver syndrome 2 +1 more	GPathogenic/Likely pathogenic
Select item 1489179	NM_020812.4(DOCK6):c.3163G>A (p.Val1055Met)	DOCK6 (V1055M +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 253048	NM_020812.4(DOCK6):c.3154G>A (p.Glu1052Lys)	DOCK6 (E1052K +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder	GUncertain significance
Select item 715788	NM_020812.4(DOCK6):c.3054G>A (p.Arg1018=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GLikely benign
Select item 1358682	NM_020812.4(DOCK6):c.3052C>T (p.Arg1018Trp)	DOCK6 (R1018W +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder +3 more	GUncertain significance
Select item 2987854	NM_020812.4(DOCK6):c.2991G>A (p.Leu997=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GLikely benign
Select item 3036548	NM_020812.4(DOCK6):c.2955+3G>A	DOCK6	Single nucleotide variant (intron variant)	DOCK6-related disorder	GLikely benign
Select item 732394	NM_020812.4(DOCK6):c.2883C>T (p.Pro961=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GBenign/Likely benign
Select item 723458	NM_020812.4(DOCK6):c.2795G>C (p.Trp932Ser)	DOCK6 (W932S +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder +2 more	GLikely benign
Select item 724419	NM_020812.4(DOCK6):c.2790C>T (p.His930=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GLikely benign
Select item 2630616	NM_020812.4(DOCK6):c.2780T>A (p.Ile927Asn)	DOCK6 (I927N +1 more)	Single nucleotide variant (missense variant)	DOCK6-related disorder	GUncertain significance
Select item 730995	NM_020812.4(DOCK6):c.2772C>G (p.Arg924=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GBenign/Likely benign
Select item 3034480	NM_020812.4(DOCK6):c.2691C>T (p.Asp897=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder	GLikely benign
Select item 792918	NM_020812.4(DOCK6):c.2628G>A (p.Ala876=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GLikely benign
Select item 593194	NM_020812.4(DOCK6):c.2594G>A (p.Arg865His)	DOCK6 (R865H)	Single nucleotide variant (missense variant)	DOCK6-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 764967	NM_020812.4(DOCK6):c.2514C>T (p.Tyr838=)	DOCK6	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 771512	NM_020812.4(DOCK6):c.2506G>A (p.Val836Ile)	DOCK6 (V836I)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 737455	NM_020812.4(DOCK6):c.2505C>T (p.Tyr835=)	DOCK6	Single nucleotide variant (synonymous variant)	Adams-Oliver syndrome 2 +2 more	GLikely benign
Select item 1911965	NM_020812.4(DOCK6):c.2480G>T (p.Gly827Val)	DOCK6 (G827V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 710755	NM_020812.4(DOCK6):c.2476C>T (p.Arg826Cys)	DOCK6 (R826C)	Single nucleotide variant (missense variant)	DOCK6-related disorder +1 more	GBenign
Select item 741030	NM_020812.4(DOCK6):c.2373G>C (p.Pro791=)	DOCK6	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2999172	NM_020812.4(DOCK6):c.2350G>C (p.Val784Leu)	DOCK6 (V784L)	Single nucleotide variant (missense variant)	DOCK6-related disorder +1 more	GUncertain significance
Select item 1707220	NM_020812.4(DOCK6):c.2346G>A (p.Lys782=)	DOCK6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1982733	NM_020812.4(DOCK6):c.2250G>C (p.Glu750Asp)	DOCK6 (E750D)	Single nucleotide variant (missense variant)	DOCK6-related disorder +1 more	GUncertain significance
Select item 2166284	NM_020812.4(DOCK6):c.2140G>A (p.Val714Met)	DOCK6 (V714M)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 523606	NM_020812.4(DOCK6):c.2104G>A (p.Gly702Ser)	DOCK6 (G702S)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 726430	NM_020812.4(DOCK6):c.2103C>T (p.Asp701=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GBenign/Likely benign
Select item 3044096	NM_020812.4(DOCK6):c.2096G>A (p.Trp699Ter)	DOCK6 (W699*)	Single nucleotide variant (nonsense)	DOCK6-related disorder	GLikely pathogenic
Select item 3029472	NM_020812.4(DOCK6):c.2010C>T (p.Gly670=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder	GLikely benign
Select item 719303	NM_020812.4(DOCK6):c.1993G>A (p.Gly665Arg)	DOCK6 (G665R)	Single nucleotide variant (missense variant)	DOCK6-related disorder +1 more	GBenign/Likely benign
Select item 719116	NM_020812.4(DOCK6):c.1643+5G>A	DOCK6	Single nucleotide variant (intron variant)	DOCK6-related disorder +1 more	GBenign/Likely benign
Select item 715181	NM_020812.4(DOCK6):c.1608C>T (p.Pro536=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GBenign/Likely benign
Select item 3031481	NM_020812.4(DOCK6):c.1594A>G (p.Ile532Val)	DOCK6 (I532V)	Single nucleotide variant (missense variant)	DOCK6-related disorder	GUncertain significance
Select item 1633543	NM_020812.4(DOCK6):c.1572C>T (p.Pro524=)	DOCK6	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 771212	NM_020812.4(DOCK6):c.1289G>A (p.Arg430His)	DOCK6 (R430H)	Single nucleotide variant (missense variant)	DOCK6-related disorder +2 more	GLikely benign
Select item 444447	NM_020812.4(DOCK6):c.906G>C (p.Ser302=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GBenign/Likely benign
Select item 3036973	NM_020812.4(DOCK6):c.874-3C>T	DOCK6	Single nucleotide variant (intron variant)	DOCK6-related disorder	GLikely benign
Select item 729645	NM_020812.4(DOCK6):c.810C>T (p.Phe270=)	DOCK6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 261359	NM_020812.4(DOCK6):c.749C>T (p.Pro250Leu)	DOCK6 (P250L)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 782054	NM_020812.4(DOCK6):c.744C>T (p.Ser248=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GLikely benign
Select item 757523	NM_020812.4(DOCK6):c.729C>G (p.Ala243=)	DOCK6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3036704	NM_020812.4(DOCK6):c.720+4G>A	DOCK6	Single nucleotide variant (intron variant)	DOCK6-related disorder	GLikely benign
Select item 2192612	NM_020812.4(DOCK6):c.707C>T (p.Pro236Leu)	DOCK6 (P236L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1579172	NM_020812.4(DOCK6):c.687G>A (p.Pro229=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder +1 more	GLikely benign
Select item 2055529	NM_020812.4(DOCK6):c.633C>T (p.Ala211=)	DOCK6	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2179862	NM_020812.4(DOCK6):c.520C>T (p.Arg174Cys)	DOCK6 (R174C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3033222	NM_020812.4(DOCK6):c.459C>T (p.Val153=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder	GLikely benign
Select item 376838	NM_020812.4(DOCK6):c.434G>A (p.Arg145Gln)	DOCK6 (R145Q)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3052244	NM_020812.4(DOCK6):c.397G>A (p.Ala133Thr)	DOCK6 (A133T)	Single nucleotide variant (missense variant)	DOCK6-related disorder	GUncertain significance
Select item 261356	NM_020812.4(DOCK6):c.377+12T>A	DOCK6	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 2718276	NM_020812.4(DOCK6):c.172G>T (p.Asp58Tyr)	DOCK6 (D58Y)	Single nucleotide variant (missense variant)	DOCK6-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 710944	NM_020812.4(DOCK6):c.133G>A (p.Val45Ile)	DOCK6 (V45I)	Single nucleotide variant (missense variant)	DOCK6-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 1028687	NM_020812.4(DOCK6):c.100C>G (p.His34Asp)	DOCK6 (H34D)	Single nucleotide variant (missense variant)	DOCK6-related disorder +2 more	GUncertain significance
Select item 3045506	NM_020812.4(DOCK6):c.99C>T (p.Pro33=)	DOCK6	Single nucleotide variant (synonymous variant)	DOCK6-related disorder	GLikely benign
Select item 1613639	NM_020812.4(DOCK6):c.12C>G (p.Ser4=)	DOCK6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 94