"PreventionGenetics, part of Exact Sciences"[submitter] AND "DOCK6-AS1 - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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

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: 22