Related gene-specific medical variations for Gene (Select 9921) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3314657	NM_014868.5(RNF10):c.59G>C (p.Gly20Ala)	LOC128071547, RNF10 (G20A)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3154908	NM_014868.5(RNF10):c.53A>G (p.Asn18Ser)	LOC128071547, RNF10 (N18S)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3154906	NM_014868.5(RNF10):c.31A>G (p.Thr11Ala)	LOC128071547, RNF10 (H49R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608853	NM_014868.5(RNF10):c.82T>A (p.Ser28Thr)	LOC128071547, RNF10 (S28T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534525	NM_014868.5(RNF10):c.65A>G (p.Asn22Ser)	LOC128071547, RNF10 (N22S)	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2329502	NM_014868.5(RNF10):c.57C>A (p.Ser19Arg)	LOC128071547, RNF10 (S19R)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2217483	NM_014868.5(RNF10):c.142T>G (p.Ser48Ala)	LOC128071547, RNF10 (S48A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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