"Ambry Genetics"[submitter] AND "LOC130067175"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3088586	NM_133455.4(EMID1):c.76G>C (p.Gly26Arg)	EMID1, LOC130067175 (G26R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517959	NM_133455.4(EMID1):c.76G>A (p.Gly26Arg)	EMID1, LOC130067175 (G26R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530048	NM_133455.4(EMID1):c.82G>A (p.Ala28Thr)	EMID1, LOC130067175 (A28T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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