"Ambry Genetics"[submitter] AND "LOC129936166"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3172646	NM_133625.6(SYN2):c.1411G>T (p.Val471Leu)	LOC129936166, SYN2 (V471L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394950	NM_133625.6(SYN2):c.1426C>T (p.Arg476Trp)	LOC129936166, SYN2 (R476W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460416	NM_133625.6(SYN2):c.1481C>T (p.Ser494Phe)	LOC129936166, SYN2 (S494F)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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ClinVar