"Ambry Genetics"[submitter] AND "NXF5"[gene] - ClinVar

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Search results

Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2366999	NR_028089.1(NXF5):n.1382A>G	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3203487	NR_028089.1(NXF5):n.1370C>T	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3203495	NR_028089.1(NXF5):n.1264A>G	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2289400	NR_028089.1(NXF5):n.1082A>C	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2541424	NR_028089.1(NXF5):n.1049C>T	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3203493	NR_028089.1(NXF5):n.1013G>A	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3203492	NR_028089.1(NXF5):n.983G>A	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2320176	NR_028089.1(NXF5):n.919G>T	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3203491	NR_028089.1(NXF5):n.862A>C	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2592179	NR_028089.1(NXF5):n.811C>A	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2405430	NR_028089.1(NXF5):n.788G>A	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 1205899	NR_028089.1(NXF5):n.775A>G	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3203489	NR_028089.1(NXF5):n.719C>G	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2354309	NR_028089.1(NXF5):n.526T>C	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2713448	NR_028089.1(NXF5):n.514C>T	NXF5	Single nucleotide variant (non-coding transcript variant)	not provided +1 more	GUncertain significance
Select item 2302496	NR_028089.1(NXF5):n.507C>G	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2357503	NR_028089.1(NXF5):n.488C>T	NXF5	Single nucleotide variant (non-coding transcript variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2618865	NR_028089.1(NXF5):n.466A>C	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign
Select item 2353478	NR_028089.1(NXF5):n.462G>C	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2596598	NR_028089.1(NXF5):n.390G>A	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3203494	NR_028089.1(NXF5):n.368G>A	NXF5	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign

ClinVar

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Items: 21