"GeneDx"[submitter] AND "AXL"[gene] - ClinVar

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Search results

Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1181285	NC_000019.10:g.41218915G>A	AXL	Single nucleotide variant	not provided	GBenign
Select item 1271413	NC_000019.10:g.41218980G>A	AXL	Single nucleotide variant	not provided	GBenign
Select item 1248751	NM_021913.5(AXL):c.-27A>G	AXL	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1248203	NM_021913.5(AXL):c.85+28G>A	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280233	NM_021913.5(AXL):c.86-87G>A	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273080	NM_021913.5(AXL):c.409+46C>T	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225895	NM_021913.5(AXL):c.410-293C>A	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261254	NM_021913.5(AXL):c.410-156T>C	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1256702	NM_021913.5(AXL):c.667+65G>A	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245530	NM_021913.5(AXL):c.783+126G>T	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288205	NM_021913.5(AXL):c.783+141C>T	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236496	NM_021913.5(AXL):c.783+207C>T	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245024	NM_021913.5(AXL):c.783+211G>A	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250954	NM_021913.5(AXL):c.994+42G>T	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237789	NM_021913.5(AXL):c.1135-238C>T	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222049	NM_021913.5(AXL):c.1285+62C>G	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1181400	NM_021913.5(AXL):c.1286-185C>T	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228346	NM_021913.5(AXL):c.1286-159G>A	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1223277	NM_021913.5(AXL):c.1286-111_1286-87del	AXL	Deletion (intron variant)	not provided	GBenign
Select item 1227439	NM_021913.5(AXL):c.1286-59G>A	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252630	NM_021913.5(AXL):c.1312+305C>T	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236802	NM_021913.5(AXL):c.1313-35T>C	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291791	NM_021913.5(AXL):c.1445+125C>T	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264615	NM_021913.5(AXL):c.1445+128G>T	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1183580	NM_021913.5(AXL):c.1538-202G>T	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247722	NM_021913.5(AXL):c.1712-223del	AXL	Deletion (intron variant)	not provided	GBenign
Select item 1295161	NM_021913.5(AXL):c.1712-209_1712-208del	AXL	Deletion (intron variant)	not provided	GBenign
Select item 1250328	NM_021913.5(AXL):c.1927-30C>T	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265103	NM_021913.5(AXL):c.2036+24C>T	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261931	NM_021913.5(AXL):c.2196+9A>G	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1223299	NM_021913.5(AXL):c.2196+154T>C	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1255106	NM_021913.5(AXL):c.2196+184del	AXL	Deletion (intron variant)	not provided	GBenign
Select item 1235653	NM_021913.5(AXL):c.2333+97A>G	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280970	NM_021913.5(AXL):c.2334-229T>C	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1243527	NM_021913.5(AXL):c.2334-51A>C	AXL	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 781486	NM_021913.5(AXL):c.2451C>T (p.Asp817=)	AXL	Single nucleotide variant (synonymous variant)	not provided	GBenign

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Items: 36