"PreventionGenetics, part of Exact Sciences"[submitter] AND "DLX6"[gen - ClinVar - NCBI

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

Search results

Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2915783	NM_005222.4(DLX6):c.75GCA[12] (p.Gln44_Pro45insGlnGlnGlnGln)	DLX6, DLX6-AS1	Microsatellite (inframe_insertion)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1476323	NM_005222.4(DLX6):c.75GCA[9] (p.Gln44dup)	DLX6, DLX6-AS1	Microsatellite (inframe_insertion)	DLX6-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 2041393	NM_005222.4(DLX6):c.75GCA[6] (p.Gln43_Gln44del)	DLX6, DLX6-AS1	Microsatellite (inframe_deletion)	DLX6-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 2041446	NM_005222.4(DLX6):c.93G>A (p.Gln31=)	DLX6, DLX6-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2053894	NM_005222.4(DLX6):c.102GCA[8] (p.Gln44_Pro45insGln)	DLX6, DLX6-AS1	Microsatellite (inframe_insertion)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1600917	NM_005222.4(DLX6):c.134CGC[8] (p.Pro53del)	DLX6, DLX6-AS1 (P53del)	Microsatellite (inframe_deletion)	DLX6-related disorder +1 more	GBenign/Likely benign
Select item 1595843	NM_005222.4(DLX6):c.134CGC[5] (p.Pro50_Pro53del)	DLX6, DLX6-AS1	Microsatellite (inframe_deletion)	not provided +1 more	GBenign/Likely benign
Select item 774129	NM_005222.4(DLX6):c.134CGC[6] (p.Pro51_Pro53del)	DLX6, DLX6-AS1	Microsatellite (inframe_deletion)	DLX6-related disorder +1 more	GBenign
Select item 2064954	NM_005222.4(DLX6):c.228GGC[6] (p.Ala83_Gly84insAla)	DLX6, DLX6-AS1	Microsatellite (inframe_insertion)	not provided +1 more	GLikely benign
Select item 3041468	NM_005222.4(DLX6):c.243A>G (p.Ala81=)	DLX6, DLX6-AS1	Single nucleotide variant (synonymous variant)	DLX6-related disorder	GLikely benign
Select item 3036242	NM_005222.4(DLX6):c.291C>T (p.Gly97=)	DLX6, DLX6-AS1	Single nucleotide variant (synonymous variant)	DLX6-related disorder	GLikely benign
Select item 3050908	NM_005222.4(DLX6):c.333C>G (p.Arg111=)	DLX6, DLX6-AS1 +1 more	Single nucleotide variant (synonymous variant)	DLX6-related disorder	GLikely benign
Select item 2905420	NM_005222.4(DLX6):c.720C>T (p.Gly240=)	DLX6, DLX6-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2721208	NM_005222.4(DLX6):c.841T>A (p.Ser281Thr)	DLX6, DLX6-AS1 (S281T)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign