"Ambry Genetics"[submitter] AND "H3C3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3103937	NM_003531.3(H3C3):c.68C>G (p.Thr23Ser)	H3C3, LOC129996012 (T23S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103939	NM_003531.3(H3C3):c.73G>A (p.Ala25Thr)	H3C3, LOC129996012 (A25T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283362	NM_003531.3(H3C3):c.199C>T (p.Pro67Ser)	H3C3, LOC129996012 (P67S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509481	NM_003531.3(H3C3):c.204C>A (p.Phe68Leu)	H3C3, LOC129996012 (F68L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549756	NM_003531.3(H3C3):c.214G>C (p.Val72Leu)	H3C3, LOC129996012 (V72L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103935	NM_003531.3(H3C3):c.319G>C (p.Asp107His)	H3C3, LOC129996012 (D107H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103936	NM_003531.3(H3C3):c.382G>C (p.Ala128Pro)	H3C3 (A128P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616674	NM_003531.3(H3C3):c.388C>T (p.Arg130Cys)	H3C3 (R130C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar