"Ambry Genetics"[submitter] AND "SNX16"[gene] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2618310	NM_152836.3(SNX16):c.968G>A (p.Ser323Asn)	SNX16 (S323N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2311619	NM_152836.3(SNX16):c.967A>G (p.Ser323Gly)	SNX16 (S323G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167170	NM_152836.3(SNX16):c.952C>A (p.Pro318Thr)	SNX16 (P318T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489244	NM_152836.3(SNX16):c.948T>A (p.Asn316Lys)	SNX16 (N287K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252929	NM_152836.3(SNX16):c.941C>G (p.Ala314Gly)	SNX16 (A285G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325117	NM_152836.3(SNX16):c.940G>C (p.Ala314Pro)	SNX16 (A285P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546095	NM_152836.3(SNX16):c.901C>G (p.Leu301Val)	SNX16 (L272V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2523294	NM_152836.3(SNX16):c.805G>C (p.Glu269Gln)	SNX16 (E240Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167169	NM_152836.3(SNX16):c.734T>C (p.Leu245Pro)	SNX16 (L245P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2523362	NM_152836.3(SNX16):c.701A>G (p.Glu234Gly)	SNX16 (E205G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463491	NM_152836.3(SNX16):c.653G>A (p.Gly218Asp)	SNX16 (G189D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228877	NM_152836.3(SNX16):c.631C>G (p.Leu211Val)	SNX16 (L182V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335308	NM_152836.3(SNX16):c.598G>A (p.Asp200Asn)	SNX16 (D200N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167168	NM_152836.3(SNX16):c.544G>A (p.Glu182Lys)	SNX16 (E153K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252453	NM_152836.3(SNX16):c.527A>G (p.Tyr176Cys)	SNX16 (Y147C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524851	NM_152836.3(SNX16):c.338T>C (p.Leu113Pro)	SNX16 (L113P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556195	NM_152836.3(SNX16):c.304A>G (p.Asn102Asp)	SNX16 (N73D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2523131	NM_152836.3(SNX16):c.286C>A (p.Gln96Lys)	SNX16 (Q67K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167167	NM_152836.3(SNX16):c.199G>A (p.Val67Ile)	SNX16 (V67I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3167166	NM_152836.3(SNX16):c.194C>T (p.Ser65Leu)	SNX16 (S65L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3167165	NM_152836.3(SNX16):c.185A>C (p.Asp62Ala)	SNX16 (D62A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 21