ARL15[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3129542	NM_019087.3(ARL15):c.499G>A (p.Gly167Arg)	ARL15 (G167R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465790	NM_019087.3(ARL15):c.484G>C (p.Glu162Gln)	ARL15 (E162Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129541	NM_019087.3(ARL15):c.425A>G (p.Asn142Ser)	ARL15 (N142S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129540	NM_019087.3(ARL15):c.347T>C (p.Leu116Ser)	ARL15 (L116S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2630875	NM_019087.3(ARL15):c.253+3A>T	ARL15	Single nucleotide variant (intron variant)	ARL15-related disorder	GUncertain significance
Select item 2541515	NM_019087.3(ARL15):c.124G>A (p.Gly42Ser)	ARL15 (G42S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129543	NM_019087.3(ARL15):c.95A>T (p.Glu32Val)	ARL15 (E32V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556441	NM_019087.3(ARL15):c.89G>A (p.Arg30Gln)	ARL15 (R30Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3060130	NM_019087.3(ARL15):c.15A>G (p.Arg5=)	ARL15	Single nucleotide variant (synonymous variant)	ARL15-related disorder	GBenign
Select item 689313	GRCh37/hg19 5q11.2(chr5:53287547-53721555)x3	ARL15	Copy number gain	not provided	GUncertain significance
Select item 563064	GRCh37/hg19 5q11.2(chr5:53300747-53662628)x3	ARL15	Copy number gain	not provided	GUncertain significance
Select item 446347	GRCh37/hg19 5q11.2(chr5:53326381-53739530)x3	ARL15	Copy number gain	See cases	GUncertain significance
Select item 442375	GRCh37/hg19 5q11.2(chr5:53141338-53730978)x3	ARL15	Copy number gain	See cases	GUncertain significance