"Ambry Genetics"[submitter] AND "ARL16"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3129548	NM_001040025.3(ARL16):c.500C>T (p.Ala167Val)	ARL16 (A105V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129547	NM_001040025.3(ARL16):c.457C>T (p.Arg153Cys)	ARL16 (R153C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477743	NM_001040025.3(ARL16):c.454G>A (p.Ala152Thr)	ARL16 (A90T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532233	NM_001040025.3(ARL16):c.437C>T (p.Thr146Ile)	ARL16 (T146I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129545	NM_001040025.3(ARL16):c.368T>C (p.Met123Thr)	ARL16 (M123T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491096	NM_001040025.3(ARL16):c.340T>C (p.Phe114Leu)	ARL16 (F114L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402232	NM_001040025.3(ARL16):c.298C>T (p.Leu100Phe)	ARL16 (L38F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317338	NM_001040025.3(ARL16):c.206G>A (p.Ser69Asn)	ARL16 (S7N +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2596591	NM_001040025.3(ARL16):c.201G>T (p.Trp67Cys)	ARL16 (W5C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2512281	NM_001040025.3(ARL16):c.136A>G (p.Thr46Ala)	ARL16 (T46A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2382752	NM_001040025.3(ARL16):c.134T>G (p.Leu45Arg)	ARL16 (L45R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2262287	NM_001040025.3(ARL16):c.101C>A (p.Pro34Gln)	ARL16 (P34Q)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3129544	NM_001040025.3(ARL16):c.38C>T (p.Thr13Met)	ARL16, LOC112533681 (T13M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2484957	NM_001040025.3(ARL16):c.8T>C (p.Leu3Pro)	ARL16, LOC112533681 (L3P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129549	NM_001040025.3(ARL16):c.-3G>A	ARL16, LOC112533681	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2241184	NM_001040025.3(ARL16):c.-20C>A	ARL16, LOC112533681	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance