"Ambry Genetics"[submitter] AND "LOC126861126"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3324068	NM_175733.4(SYT9):c.1288G>A (p.Glu430Lys)	LOC126861126, SYT9 (E430K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283457	NM_175733.4(SYT9):c.1302A>T (p.Gln434His)	LOC126861126, SYT9 (Q434H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248962	NM_175733.4(SYT9):c.1336C>T (p.Arg446Cys)	LOC126861126, SYT9 (R446C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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