"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZNF454"[g - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 788529	NM_000843.4(GRM6):c.2588C>T (p.Thr863Met)	GRM6, ZNF454 (T863M)	Single nucleotide variant (missense variant)	GRM6-related disorder +1 more	GLikely benign
Select item 1082514	NM_000843.4(GRM6):c.2340C>T (p.Asn780=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	GRM6-related disorder +1 more	GLikely benign
Select item 374582	NM_000843.4(GRM6):c.2257G>A (p.Gly753Ser)	ZNF454, GRM6 (G753S)	Single nucleotide variant (missense variant)	GRM6-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 729466	NM_000843.4(GRM6):c.2124+8C>T	GRM6, ZNF454	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1093748	NM_000843.4(GRM6):c.2061A>G (p.Thr687=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	GRM6-related disorder +1 more	GLikely benign
Select item 99638	NM_000843.4(GRM6):c.1953C>T (p.Ala651=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	GRM6-related disorder +2 more	GBenign/Likely benign
Select item 725523	NM_000843.4(GRM6):c.1944G>A (p.Ala648=)	ZNF454, GRM6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 93439	NM_000843.4(GRM6):c.1875C>T (p.Tyr625=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 99632	NM_000843.4(GRM6):c.1732C>T (p.Arg578Cys)	GRM6, ZNF454 (R578C)	Single nucleotide variant (missense variant)	GRM6-related disorder +2 more	GBenign/Likely benign
Select item 1095066	NM_000843.4(GRM6):c.1707G>C (p.Thr569=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	GRM6-related disorder +1 more	GLikely benign
Select item 716636	NM_000843.4(GRM6):c.1665C>T (p.Cys555=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 730258	NM_000843.4(GRM6):c.1653C>T (p.Asp551=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1583156	NM_000843.4(GRM6):c.1545G>A (p.Ser515=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 750443	NM_000843.4(GRM6):c.1532A>G (p.His511Arg)	ZNF454, GRM6 (H511R)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1135022	NM_000843.4(GRM6):c.1524C>T (p.Gly508=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	GRM6-related disorder +1 more	GLikely benign
Select item 1671023	NM_000843.4(GRM6):c.1501-10T>C	GRM6, ZNF454	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1090075	NM_000843.4(GRM6):c.1401C>T (p.Pro467=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1132130	NM_000843.4(GRM6):c.1389C>T (p.Asn463=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	GRM6-related disorder +1 more	GLikely benign
Select item 1085990	NM_000843.4(GRM6):c.1149C>T (p.Cys383=)	GRM6, ZNF454	Single nucleotide variant (synonymous variant)	GRM6-related disorder +1 more	GLikely benign