"Genome-Nilou Lab"[submitter] AND "ATL3"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 474837	NM_015459.5(ATL3):c.1599A>G (p.Arg533=)	ATL3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1237757	NM_015459.5(ATL3):c.1539+14_1539+16del	ATL3	Microsatellite (intron variant)	Neuropathy, hereditary sensory, type 1F +1 more	GBenign
Select item 474834	NM_015459.5(ATL3):c.1434A>G (p.Gly478=)	ATL3	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1166867	NM_015459.5(ATL3):c.1107+5G>A	ATL3	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 474841	NM_015459.5(ATL3):c.978+7dup	ATL3	Duplication (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 541689	NM_015459.5(ATL3):c.712-8A>G	ATL3	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1293186	NM_015459.5(ATL3):c.712-18C>G	ATL3	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1599122	NM_015459.5(ATL3):c.618+13_618+16del	ATL3	Microsatellite (intron variant)	Neuropathy, hereditary sensory, type 1F	GBenign
Select item 1263608	NM_015459.5(ATL3):c.510+63G>A	ATL3	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 474839	NM_015459.5(ATL3):c.418C>T (p.Leu140=)	ATL3	Single nucleotide variant (synonymous variant)	Neuropathy, hereditary sensory, type 1F +1 more	GBenign/Likely benign
Select item 701888	NM_015459.5(ATL3):c.31G>T (p.Ala11Ser)	ATL3 (A11S)	Single nucleotide variant (missense variant +1 more)	Neuropathy, hereditary sensory, type 1F +1 more	GBenign