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

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Items: 46

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2334061	NM_000250.2(MPO):c.2182G>T (p.Val728Phe)	MPO (V728F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295713	NM_000250.2(MPO):c.2134G>A (p.Val712Met)	MPO (V712M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334422	NM_000250.2(MPO):c.2125A>T (p.Ile709Phe)	MPO (I709F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202604	NM_000250.2(MPO):c.2113G>A (p.Asp705Asn)	MPO (D705N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258797	NM_000250.2(MPO):c.1996G>C (p.Gly666Arg)	MPO (G666R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202599	NM_000250.2(MPO):c.1984G>A (p.Ala662Thr)	MPO (A662T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509454	NM_000250.2(MPO):c.1973G>A (p.Gly658Asp)	MPO (G658D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286183	NM_000250.2(MPO):c.1969G>T (p.Val657Leu)	MPO (V657L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295711	NM_000250.2(MPO):c.1936G>A (p.Gly646Ser)	MPO (G646S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364565	NM_000250.2(MPO):c.1918A>T (p.Ile640Phe)	MPO (I640F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345556	NM_000250.2(MPO):c.1918A>G (p.Ile640Val)	MPO (I640V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202586	NM_000250.2(MPO):c.1815C>A (p.Phe605Leu)	MPO (F605L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202580	NM_000250.2(MPO):c.1780C>T (p.His594Tyr)	LOC106694316, MPO (H594Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474160	NM_000250.2(MPO):c.1769G>A (p.Arg590His)	LOC106694316, MPO (R590H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607105	NM_000250.2(MPO):c.1738G>A (p.Gly580Arg)	LOC106694316, MPO (G580R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528487	NM_000250.2(MPO):c.1636A>G (p.Ile546Val)	LOC106694316, MPO (I546V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318830	NM_000250.2(MPO):c.1535T>C (p.Leu512Pro)	LOC106694316, MPO (L512P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483780	NM_000250.2(MPO):c.1528T>C (p.Phe510Leu)	LOC106694316, MPO (F510L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295712	NM_000250.2(MPO):c.1477G>A (p.Val493Ile)	LOC106694316, MPO (V493I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278742	NM_000250.2(MPO):c.1471G>A (p.Ala491Thr)	LOC106694316, MPO (A491T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202552	NM_000250.2(MPO):c.1367T>C (p.Ile456Thr)	LOC106694316, MPO (I456T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384553	NM_000250.2(MPO):c.1273C>T (p.Arg425Trp)	LOC106694316, MPO (R425W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202543	NM_000250.2(MPO):c.1250C>A (p.Thr417Asn)	LOC106694316, MPO (T417N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378375	NM_000250.2(MPO):c.1181C>T (p.Ala394Val)	MPO (A394V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2288490	NM_000250.2(MPO):c.1039G>A (p.Glu347Lys)	MPO (E347K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297696	NM_000250.2(MPO):c.896A>G (p.Asn299Ser)	MPO (N299S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364428	NM_000250.2(MPO):c.856G>T (p.Val286Phe)	MPO (V286F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202644	NM_000250.2(MPO):c.826G>A (p.Val276Ile)	MPO (V276I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296587	NM_000250.2(MPO):c.815G>A (p.Arg272Gln)	MPO (R272Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202641	NM_000250.2(MPO):c.814C>T (p.Arg272Trp)	MPO (R272W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319953	NM_000250.2(MPO):c.757A>G (p.Met253Val)	MPO (M253V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614383	NM_000250.2(MPO):c.731C>T (p.Pro244Leu)	MPO (P244L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202638	NM_000250.2(MPO):c.686C>G (p.Ala229Gly)	MPO (A229G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202635	NM_000250.2(MPO):c.685G>A (p.Ala229Thr)	MPO (A229T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262257	NM_000250.2(MPO):c.608A>C (p.Tyr203Ser)	MPO (Y203S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483686	NM_000250.2(MPO):c.571T>A (p.Ser191Thr)	MPO (S191T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202626	NM_000250.2(MPO):c.517T>C (p.Tyr173His)	MPO (Y173H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3295710	NM_000250.2(MPO):c.490G>A (p.Gly164Arg)	MPO (G164R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547375	NM_000250.2(MPO):c.458C>T (p.Ser153Phe)	LOC106694315, MPO (S153F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467364	NM_000250.2(MPO):c.449A>T (p.Asn150Ile)	LOC106694315, MPO (N150I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330671	NM_000250.2(MPO):c.422C>T (p.Thr141Ile)	LOC106694315, MPO (T141I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202616	NM_000250.2(MPO):c.381G>C (p.Glu127Asp)	LOC106694315, MPO (E127D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482702	NM_000250.2(MPO):c.314C>T (p.Pro105Leu)	LOC106694315, MPO (P105L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299695	NM_000250.2(MPO):c.224A>G (p.Lys75Arg)	LOC106694315, MPO (K75R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468154	NM_000250.2(MPO):c.179C>T (p.Ser60Leu)	LOC106694315, MPO (S60L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553781	NM_000250.2(MPO):c.112G>T (p.Ala38Ser)	LOC106694315, MPO (A38S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 46