H2AC4[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3103740	NM_003513.3(H2AC4):c.235A>G (p.Ile79Val)	H2AC4 (I79V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103739	NM_003513.3(H2AC4):c.222C>G (p.Asn74Lys)	H2AC4 (N74K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103738	NM_003513.3(H2AC4):c.206A>G (p.Asn69Ser)	H2AC4 (N69S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103737	NM_003513.3(H2AC4):c.205A>G (p.Asn69Asp)	H2AC4 (N69D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656293	NM_003513.3(H2AC4):c.189C>T (p.Ile63=)	H2AC4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2516802	NM_003513.3(H2AC4):c.179C>T (p.Thr60Ile)	H2AC4 (T60I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103736	NM_003513.3(H2AC4):c.158C>T (p.Ala53Val)	H2AC4 (A53V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103735	NM_003513.3(H2AC4):c.124G>C (p.Glu42Gln)	H2AC4 (E42Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103734	NM_003513.3(H2AC4):c.116A>G (p.Asn39Ser)	H2AC4 (N39S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602778	NM_003513.3(H2AC4):c.107G>A (p.Arg36His)	H2AC4 (R36H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512334	NM_003513.3(H2AC4):c.95A>C (p.His32Pro)	H2AC4 (H32P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457353	NM_003513.3(H2AC4):c.77T>A (p.Phe26Tyr)	H2AC4 (F26Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599474	NM_003513.3(H2AC4):c.65C>T (p.Ala22Val)	H2AC4 (A22V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462787	NM_003513.3(H2AC4):c.53G>A (p.Arg18Gln)	H2AC4 (R18Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103741	NM_003513.3(H2AC4):c.43G>A (p.Ala15Thr)	H2AC4 (A15T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595131	NM_003513.3(H2AC4):c.37G>A (p.Ala13Thr)	H2AC4 (A13T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467471	NM_003513.3(H2AC4):c.5C>T (p.Ser2Phe)	H2AC4 (S2F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance