"Ambry Genetics"[submitter] AND "H3-5"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3103901	NM_001013699.3(H3-5):c.386G>A (p.Arg129Gln)	H3-5 (R129Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511039	NM_001013699.3(H3-5):c.283G>A (p.Ala95Thr)	H3-5 (A95T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103900	NM_001013699.3(H3-5):c.272C>T (p.Ala91Val)	H3-5 (A91V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463388	NM_001013699.3(H3-5):c.265G>A (p.Val89Ile)	H3-5 (V89I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103899	NM_001013699.3(H3-5):c.197C>A (p.Pro66His)	H3-5 (P66H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103898	NM_001013699.3(H3-5):c.182T>C (p.Leu61Pro)	H3-5 (L61P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600209	NM_001013699.3(H3-5):c.157C>G (p.Arg53Gly)	H3-5 (R53G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598110	NM_001013699.3(H3-5):c.148G>A (p.Glu50Lys)	H3-5 (E50K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103902	NM_001013699.3(H3-5):c.53G>A (p.Arg18His)	H3-5 (R18H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491449	NM_001013699.3(H3-5):c.52C>A (p.Arg18Ser)	H3-5 (R18S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance