Related gene-specific medical variations for Gene (Select 8351) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3283311	NM_021065.3(H2AC7):c.107G>A (p.Arg36His)	H2AC7, H3C4 +1 more (R36H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3283310	NM_021065.3(H2AC7):c.20A>G (p.Gln7Arg)	H2AC7, H3C4 +1 more (Q7R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3103751	NM_021065.3(H2AC7):c.50C>A (p.Thr17Asn)	H2AC7, H3C4 +1 more (T17N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3103750	NM_021065.3(H2AC7):c.374A>G (p.His125Arg)	H2AC7, H3C4 +1 more (H125R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3103749	NM_021065.3(H2AC7):c.374A>C (p.His125Pro)	H2AC7, H3C4 +1 more (H125P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3103748	NM_021065.3(H2AC7):c.280C>G (p.Leu94Val)	H2AC7, H3C4 +1 more (L94V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3103747	NM_021065.3(H2AC7):c.211G>C (p.Ala71Pro)	H2AC7, H3C4 +1 more (A71P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3103746	NM_021065.3(H2AC7):c.206A>C (p.Asn69Thr)	H2AC7, H3C4 +1 more (N69T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3103745	NM_021065.3(H2AC7):c.148G>T (p.Val50Leu)	H2AC7, H3C4 +1 more (V50L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3103744	NM_021065.3(H2AC7):c.10C>T (p.Arg4Cys)	H2AC7, H3C4 +1 more (R4C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2614817	NM_021065.3(H2AC7):c.67G>A (p.Gly23Arg)	H2AC7, H3C4 +1 more (G23R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2568770	NM_021065.3(H2AC7):c.80C>T (p.Pro27Leu)	H2AC7, H3C4 +1 more (P27L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524791	NM_021065.3(H2AC7):c.74A>G (p.Gln25Arg)	H2AC7, LOC126859627 +1 more (Q25R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517176	NM_021065.3(H2AC7):c.91G>A (p.Val31Ile)	H2AC7, H3C4 +1 more (V31I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance