"GeneDx"[submitter] AND "ARL6IP1"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1231012	NM_015161.3(ARL6IP1):c.*163A>G	ARL6IP1	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 101079	NM_015161.3(ARL6IP1):c.577_580del (p.Lys193fs)	ARL6IP1 (K193fs +1 more)	Microsatellite (frameshift variant)	not provided	GLikely pathogenic
Select item 1221048	NM_015161.3(ARL6IP1):c.494-45G>A	ARL6IP1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1300711	NM_015161.3(ARL6IP1):c.494-62dup	ARL6IP1	Duplication (intron variant)	not provided	GLikely benign
Select item 1262023	NM_015161.3(ARL6IP1):c.494-62del	ARL6IP1	Deletion (intron variant)	not provided	GBenign
Select item 1223035	NM_015161.3(ARL6IP1):c.494-123C>T	ARL6IP1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1293268	NM_015161.3(ARL6IP1):c.493+236A>C	ARL6IP1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1293091	NM_015161.3(ARL6IP1):c.493+217T>C	ARL6IP1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 474863	NM_015161.3(ARL6IP1):c.490A>C (p.Ile164Leu)	ARL6IP1 (I164L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1240660	NM_015161.3(ARL6IP1):c.409-18T>C	ARL6IP1	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 61 +1 more	GBenign
Select item 1700951	NM_015161.3(ARL6IP1):c.409-86A>G	ARL6IP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 620202	NM_015161.3(ARL6IP1):c.346C>T (p.Arg116Ter)	ARL6IP1 (R116* +1 more)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic
Select item 1228112	NM_015161.3(ARL6IP1):c.291-229AC[8]	ARL6IP1	Microsatellite (intron variant)	not provided	GBenign
Select item 1292908	NM_015161.3(ARL6IP1):c.290+215T>C	ARL6IP1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235069	NM_015161.3(ARL6IP1):c.170+279A>T	ARL6IP1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242108	NM_015161.3(ARL6IP1):c.170+256T>A	ARL6IP1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1257597	NM_015161.3(ARL6IP1):c.170+12A>T	ARL6IP1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1300528	NM_015161.3(ARL6IP1):c.37-193dup	ARL6IP1	Duplication (intron variant)	not provided	GLikely benign
Select item 1293267	NM_015161.3(ARL6IP1):c.37-204C>G	ARL6IP1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244653	NM_015161.3(ARL6IP1):c.36+223A>C	ARL6IP1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1245898	NM_015161.3(ARL6IP1):c.36+104del	ARL6IP1	Deletion (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1182950	NM_015161.3(ARL6IP1):c.36+78C>G	ARL6IP1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1326124	NC_000016.10:g.18801586C>T	ARL6IP1	Single nucleotide variant	not provided	GLikely benign
Select item 1277495	NC_000016.10:g.18801589C>T	ARL6IP1	Single nucleotide variant	not provided	GBenign
Select item 1265789	NC_000016.10:g.18801808T>G	ARL6IP1	Single nucleotide variant	not provided	GBenign

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Items: 25