"PreventionGenetics, part of Exact Sciences"[submitter] AND "H4C3"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3041804	NM_003542.4(H4C3):c.12C>T (p.Arg4=)	H4C3	Single nucleotide variant (synonymous variant)	H4C3-related disorder	GLikely benign
Select item 3055006	NM_003542.4(H4C3):c.21C>A (p.Gly7=)	H4C3	Single nucleotide variant (synonymous variant)	H4C3-related disorder	GLikely benign
Select item 3034316	NM_003542.4(H4C3):c.42T>C (p.Gly14=)	H4C3	Single nucleotide variant (synonymous variant)	H4C3-related disorder	GBenign
Select item 1243107	NM_003542.4(H4C3):c.105T>C (p.Ile35=)	H4C3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3035811	NM_003542.4(H4C3):c.156T>C (p.Tyr52=)	H4C3	Single nucleotide variant (synonymous variant)	H4C3-related disorder	GLikely benign
Select item 3043652	NM_003542.4(H4C3):c.180G>A (p.Lys60=)	H4C3	Single nucleotide variant (synonymous variant)	H4C3-related disorder	GBenign
Select item 3045887	NM_003542.4(H4C3):c.270C>T (p.Ala90=)	H4C3	Single nucleotide variant (synonymous variant)	H4C3-related disorder	GLikely benign
Select item 3030693	NM_003542.4(H4C3):c.297T>G (p.Tyr99Ter)	H4C3 (Y99*)	Single nucleotide variant (nonsense)	H4C3-related disorder	GLikely pathogenic

ClinVar