"Ambry Genetics"[submitter] AND "OPRM1"[gene] - ClinVar

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Items: 39

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2406485	NM_000914.5(OPRM1):c.13G>A (p.Ala5Thr)	OPRM1 (A5T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2383422	NM_000914.5(OPRM1):c.27C>A (p.Asn9Lys)	OPRM1 (N9K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3302360	NM_000914.5(OPRM1):c.40A>G (p.Thr14Ala)	OPRM1 (T14A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3302358	NM_000914.5(OPRM1):c.112G>T (p.Asp38Tyr)	OPRM1 (D131Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3204426	NM_000914.5(OPRM1):c.160G>A (p.Gly54Arg)	OPRM1 (G147R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3204427	NM_000914.5(OPRM1):c.311C>A (p.Ala104Asp)	OPRM1 (A197D +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2469026	NM_000914.5(OPRM1):c.375C>G (p.Phe125Leu)	OPRM1 (F125L +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2219238	NM_000914.5(OPRM1):c.401C>G (p.Thr134Arg)	OPRM1 (T53R +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3302359	NM_000914.5(OPRM1):c.494T>A (p.Val165Asp)	OPRM1 (V258D +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2244156	NM_000914.5(OPRM1):c.515G>A (p.Cys172Tyr)	OPRM1 (C91Y +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2325220	NM_000914.5(OPRM1):c.519C>A (p.His173Gln)	OPRM1 (H92Q +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3204428	NM_000914.5(OPRM1):c.520C>G (p.Pro174Ala)	OPRM1 (P267A +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3204429	NM_000914.5(OPRM1):c.551G>A (p.Arg184Gln)	OPRM1 (R277Q +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2490489	NM_000914.5(OPRM1):c.557C>A (p.Ala186Asp)	OPRM1 (A86D +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2208854	NM_000914.5(OPRM1):c.764G>A (p.Gly255Glu)	OPRM1 (G255E +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2519502	NM_000914.5(OPRM1):c.778C>T (p.Arg260Cys)	OPRM1 (R160C +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2239023	NM_000914.5(OPRM1):c.823A>G (p.Arg275Gly)	OPRM1 (R275G +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2464855	NM_000914.5(OPRM1):c.824G>A (p.Arg275Lys)	OPRM1 (R175K +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3204430	NM_000914.5(OPRM1):c.979G>T (p.Gly327Cys)	OPRM1 (G327C +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2460211	NM_000914.5(OPRM1):c.993C>G (p.Ser331Arg)	OPRM1 (S331R +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2479733	NM_000914.5(OPRM1):c.997C>T (p.Leu333Phe)	OPRM1 (L252F +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2354483	NM_000914.5(OPRM1):c.1029A>C (p.Glu343Asp)	OPRM1 (E436D +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3204424	NM_000914.5(OPRM1):c.1048A>G (p.Arg350Gly)	OPRM1 (R350G +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3204425	NM_000914.5(OPRM1):c.1063C>A (p.Pro355Thr)	OPRM1 (P448T +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2459166	NM_000914.5(OPRM1):c.1115C>T (p.Thr372Ile)	OPRM1 (T372I +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2232124	NM_000914.5(OPRM1):c.1126C>T (p.Pro376Ser)	OPRM1 (P276S +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2623539	NM_000914.5(OPRM1):c.1142C>T (p.Thr381Ile)	OPRM1 (T281I +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2364195	NM_001130700.2(IPCEF1):c.1312A>G (p.Ile438Val)	IPCEF1, OPRM1 (I438V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286296	NM_001130700.2(IPCEF1):c.1080C>G (p.Ile360Met)	IPCEF1, OPRM1 (I359M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304027	NM_001130700.2(IPCEF1):c.923T>G (p.Val308Gly)	IPCEF1, OPRM1 (V308G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286295	NM_001130700.2(IPCEF1):c.783C>A (p.Asn261Lys)	IPCEF1, OPRM1 (N260K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286291	NM_001130700.2(IPCEF1):c.719C>T (p.Thr240Met)	IPCEF1, OPRM1 (T239M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286294	NM_001130700.2(IPCEF1):c.610A>G (p.Thr204Ala)	IPCEF1, OPRM1 (T203A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286289	NM_001130700.2(IPCEF1):c.517G>A (p.Ala173Thr)	IPCEF1, OPRM1 (A172T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286290	NM_001130700.2(IPCEF1):c.509C>T (p.Pro170Leu)	IPCEF1, OPRM1 (P169L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3286292	NM_001130700.2(IPCEF1):c.508C>G (p.Pro170Ala)	IPCEF1, OPRM1 (P170A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406316	NM_001130700.2(IPCEF1):c.436A>T (p.Thr146Ser)	IPCEF1, OPRM1 (T145S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397512	NM_001130700.2(IPCEF1):c.421A>C (p.Ile141Leu)	IPCEF1, OPRM1 (I141L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461541	NM_001130700.2(IPCEF1):c.413C>T (p.Ser138Leu)	IPCEF1, OPRM1 (S137L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign

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Items: 39