"Ambry Genetics"[submitter] AND "LRRC29"[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2517000	NR_172488.1(LRRC29):n.951A>G	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2330667	NR_172488.1(LRRC29):n.894C>A	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2390892	NR_172488.1(LRRC29):n.880G>A	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign
Select item 2457782	NR_172488.1(LRRC29):n.879C>T	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2287978	NR_172488.1(LRRC29):n.879C>G	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2227127	NR_172488.1(LRRC29):n.829G>A	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3120519	NR_172488.1(LRRC29):n.814C>T	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2530433	NR_172488.1(LRRC29):n.814C>G	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2356387	NR_172488.1(LRRC29):n.763T>G	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3120518	NR_172488.1(LRRC29):n.736C>T	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2368998	NR_172488.1(LRRC29):n.721C>T	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2365884	NR_172488.1(LRRC29):n.700G>A	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2513869	NR_172488.1(LRRC29):n.527G>C	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3120517	NR_172488.1(LRRC29):n.505C>T	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign
Select item 2369590	NR_172488.1(LRRC29):n.489G>A	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2399984	NR_172488.1(LRRC29):n.471G>A	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3120516	NR_172488.1(LRRC29):n.470C>A	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign
Select item 2531482	NR_172488.1(LRRC29):n.396T>C	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2381385	NR_172488.1(LRRC29):n.382C>T	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3291548	NR_172488.1(LRRC29):n.375G>A	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign
Select item 2588396	NR_172488.1(LRRC29):n.343G>A	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3291547	NR_172488.1(LRRC29):n.337G>A	LRRC29	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance

ClinVar

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Items: 22