HAT1[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2227991	NM_003642.4(HAT1):c.383C>T (p.Ser128Phe)	HAT1 (S128F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2300899	NM_003642.4(HAT1):c.450T>G (p.Ser150Arg)	HAT1 (S150R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473797	NM_003642.4(HAT1):c.483A>G (p.Ile161Met)	HAT1 (I161M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267651	NM_003642.4(HAT1):c.524A>G (p.His175Arg)	HAT1 (H175R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362853	NM_003642.4(HAT1):c.841A>T (p.Ser281Cys)	HAT1 (S281C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3104312	NM_003642.4(HAT1):c.1052A>G (p.Tyr351Cys)	HAT1 (Y351C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391910	NM_003642.4(HAT1):c.1063A>G (p.Ile355Val)	HAT1 (I355V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2318207	NM_003642.4(HAT1):c.1202G>C (p.Ser401Thr)	HAT1 (S401T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3104313	NM_003642.4(HAT1):c.1231C>T (p.Arg411Cys)	HAT1 (R411C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance