Related gene-specific medical variations for Gene (Select 653604) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3103933	NM_001123375.3(H3C13):c.329T>A (p.Leu110Gln)	H3C13, LOC129931372 (L110Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103932	NM_001123375.3(H3C13):c.262T>C (p.Ser88Pro)	H3C13, LOC129931372 (S88P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103931	NM_001123375.3(H3C13):c.209G>A (p.Arg70Gln)	H3C13, LOC129931372 (R70Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588885	NM_001123375.3(H3C13):c.240G>C (p.Lys80Asn)	H3C13, LOC129931372 (K80N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556495	NM_001123375.3(H3C13):c.67A>G (p.Thr23Ala)	H3C13, LOC129931372 (T23A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791809	NM_001123375.3(H3C13):c.198G>A (p.Leu66=)	H3C13, LOC129931372	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 719341	NM_001123375.3(H3C13):c.174T>C (p.Ser58=)	H3C13, LOC129931372	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar