"PreventionGenetics, part of Exact Sciences"[submitter] AND "HDAC6"[ge - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 731665	NM_006044.4(HDAC6):c.432T>C (p.Val144=)	HDAC6	Single nucleotide variant (synonymous variant +1 more)	HDAC6-related disorder +1 more	GBenign
Select item 3036827	NM_006044.4(HDAC6):c.632+8T>G	HDAC6	Single nucleotide variant (3 prime UTR variant +2 more)	HDAC6-related disorder	GLikely benign
Select item 3054797	NM_006044.4(HDAC6):c.807-2dup	HDAC6	Duplication (splice acceptor variant)	HDAC6-related disorder	GLikely benign
Select item 3057132	NM_006044.4(HDAC6):c.999+9G>A	HDAC6	Single nucleotide variant (non-coding transcript variant +1 more)	HDAC6-related disorder	GLikely benign
Select item 736731	NM_006044.4(HDAC6):c.1833C>T (p.His611=)	HDAC6	Single nucleotide variant (synonymous variant +1 more)	HDAC6-related disorder +1 more	GBenign
Select item 3055312	NM_006044.4(HDAC6):c.2495G>A (p.Arg832His)	HDAC6 (R832H +1 more)	Single nucleotide variant (missense variant +1 more)	HDAC6-related disorder	GBenign
Select item 1161964	NM_006044.4(HDAC6):c.2596C>T (p.Arg866Trp)	HDAC6 (R866W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 718821	NM_006044.4(HDAC6):c.3074C>T (p.Ser1025Leu)	HDAC6 (S1039L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 734749	NM_006044.4(HDAC6):c.3153G>A (p.Gly1051=)	HDAC6	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 445469	NM_006044.4(HDAC6):c.3248G>A (p.Gly1083Asp)	HDAC6 (G1083D +1 more)	Single nucleotide variant (missense variant +1 more)	HDAC6-related disorder +1 more	GLikely benign
Select item 2237838	NM_006044.4(HDAC6):c.3529A>T (p.Ile1177Phe)	HDAC6 (I1191F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3045308	NM_006044.4(HDAC6):c.3531C>T (p.Ile1177=)	HDAC6	Single nucleotide variant (synonymous variant +1 more)	HDAC6-related disorder	GLikely benign