CARD17[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2556585	NR_172520.1(CARD17):n.286A>C	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2527708	NR_172520.1(CARD17):n.268T>C	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign
Select item 2297140	NR_172520.1(CARD17):n.250T>C	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2320062	NR_172520.1(CARD17):n.242C>T	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3263302	NR_172520.1(CARD17):n.241G>T	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3137316	NR_172520.1(CARD17):n.232C>T	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3137315	NR_172520.1(CARD17):n.220G>A	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3137314	NR_172520.1(CARD17):n.217C>T	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3263303	NR_172520.1(CARD17):n.205G>T	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2557234	NR_172520.1(CARD17):n.197T>A	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2556786	NR_172520.1(CARD17):n.197T>G	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2223828	NR_172520.1(CARD17):n.188C>T	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3137313	NR_172520.1(CARD17):n.145G>A	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3263305	NR_172520.1(CARD17):n.143G>C	CARD17	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 768481	NM_001007232.1(CARD17):c.8-1G>C	CARD17	Single nucleotide variant	not provided	GBenign