C4016819[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 878187	NM_001081.4(CUBN):c.*940A>G	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299323	NM_001081.4(CUBN):c.*883G>A	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 878188	NM_001081.4(CUBN):c.*872T>C	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GBenign
Select item 299324	NM_001081.4(CUBN):c.*794A>G	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299325	NM_001081.4(CUBN):c.*786T>C	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299326	NM_001081.4(CUBN):c.*782G>A	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299327	NM_001081.4(CUBN):c.*781C>T	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GBenign
Select item 878189	NM_001081.4(CUBN):c.*769G>A	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GLikely benign
Select item 299328	NM_001081.4(CUBN):c.*737T>C	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GBenign
Select item 299329	NM_001081.4(CUBN):c.*734A>G	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 879639	NM_001081.4(CUBN):c.*669C>T	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299330	NM_001081.4(CUBN):c.*601A>G	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GBenign
Select item 879640	NM_001081.4(CUBN):c.*597A>C	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299331	NM_001081.4(CUBN):c.*564G>C	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299332	NM_001081.4(CUBN):c.*560C>T	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299333	NM_001081.4(CUBN):c.*514T>G	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299334	NM_001081.4(CUBN):c.*470T>C	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 880003	NM_001081.4(CUBN):c.*460C>A	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 880004	NM_001081.4(CUBN):c.*453A>G	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 880005	NM_001081.4(CUBN):c.*446A>G	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299335	NM_001081.4(CUBN):c.*436C>A	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299336	NM_001081.4(CUBN):c.*420C>T	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GLikely benign
Select item 299337	NM_001081.4(CUBN):c.*416G>A	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 880006	NM_001081.4(CUBN):c.*380T>C	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GLikely benign
Select item 299338	NM_001081.4(CUBN):c.*373G>T	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 877207	NM_001081.4(CUBN):c.*330G>A	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GLikely benign
Select item 299339	NM_001081.4(CUBN):c.*330G>C	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GLikely benign
Select item 299341	NM_001081.4(CUBN):c.*329C>G	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299340	NM_001081.4(CUBN):c.*329C>T	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299342	NM_001081.4(CUBN):c.*305T>G	CUBN	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 877208	NM_001081.4(CUBN):c.*304G>T	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 877209	NM_001081.4(CUBN):c.*298G>A	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299343	NM_001081.4(CUBN):c.*297C>T	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299344	NM_001081.4(CUBN):c.*281A>G	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 878250	NM_001081.4(CUBN):c.*267A>T	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299345	NM_001081.4(CUBN):c.*266C>T	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GLikely benign
Select item 299346	NM_001081.4(CUBN):c.*203C>T	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299347	NM_001081.4(CUBN):c.*195T>C	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299348	NM_001081.4(CUBN):c.*177C>G	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299350	NM_001081.4(CUBN):c.*151G>A	CUBN	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign/Likely benign
Select item 299351	NM_001081.4(CUBN):c.*134G>A	CUBN	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 299352	NM_001081.4(CUBN):c.*93C>A	CUBN	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign/Likely benign
Select item 299353	NM_001081.4(CUBN):c.*81C>A	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299354	NM_001081.4(CUBN):c.*45C>T	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1 +1 more	GBenign/Likely benign
Select item 878850	NM_001081.4(CUBN):c.*15G>A	CUBN	Single nucleotide variant (3 prime UTR variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299355	NM_001081.4(CUBN):c.10846G>A (p.Ala3616Thr)	CUBN (A3616T)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome +1 more	GUncertain significance
Select item 878851	NM_001081.4(CUBN):c.10777G>A (p.Ala3593Thr)	CUBN (A3593T)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299356	NM_001081.4(CUBN):c.10759G>A (p.Gly3587Arg)	CUBN (G3587R)	Single nucleotide variant (missense variant)	CUBN-related condition +2 more	GBenign/Likely benign
Select item 299357	NM_001081.4(CUBN):c.10752A>T (p.Pro3584=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 880057	NM_001081.4(CUBN):c.10742C>T (p.Ser3581Phe)	CUBN (S3581F)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 880058	NM_001081.4(CUBN):c.10736C>T (p.Ser3579Phe)	CUBN (S3579F)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome +3 more	GUncertain significance
Select item 880059	NM_001081.4(CUBN):c.10729G>A (p.Ala3577Thr)	CUBN (A3577T)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome +1 more	GConflicting classifications of pathogenicity
Select item 880060	NM_001081.4(CUBN):c.10728C>G (p.Asn3576Lys)	CUBN (N3576K)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 695358	NM_001081.4(CUBN):c.10656C>T (p.Asn3552=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome +2 more	GBenign/Likely benign
Select item 299358	NM_001081.4(CUBN):c.10656C>A (p.Asn3552Lys)	CUBN (N3552K)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 289333	NM_001081.4(CUBN):c.10641G>A (p.Arg3547=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome +2 more	GConflicting classifications of pathogenicity
Select item 877271	NM_001081.4(CUBN):c.10576G>A (p.Gly3526Ser)	CUBN (G3526S)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1 +2 more	GUncertain significance
Select item 695982	NM_001081.4(CUBN):c.10575C>T (p.Pro3525=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome +1 more	GConflicting classifications of pathogenicity
Select item 299359	NM_001081.4(CUBN):c.10466T>G (p.Phe3489Cys)	CUBN (F3489C)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299360	NM_001081.4(CUBN):c.10383C>T (p.Ser3461=)	CUBN	Single nucleotide variant (synonymous variant)	CUBN-related condition +3 more	GBenign/Likely benign
Select item 299361	NM_001081.4(CUBN):c.10363-3A>G	CUBN	Single nucleotide variant (intron variant)	Imerslund-Grasbeck syndrome +2 more	GUncertain significance
Select item 299362	NM_001081.4(CUBN):c.10295C>G (p.Thr3432Ser)	CUBN (T3432S)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 877272	NM_001081.4(CUBN):c.10293C>T (p.His3431=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome type 1 +1 more	GConflicting classifications of pathogenicity
Select item 299363	NM_001081.4(CUBN):c.10267G>A (p.Val3423Ile)	CUBN (V3423I)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 299364	NM_001081.4(CUBN):c.10265C>T (p.Thr3422Ile)	CUBN (T3422I)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 299365	NM_001081.4(CUBN):c.10245C>T (p.Tyr3415=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome +1 more	GConflicting classifications of pathogenicity
Select item 878312	NM_001081.4(CUBN):c.10238A>G (p.Asp3413Gly)	CUBN (D3413G)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299366	NM_001081.4(CUBN):c.10181-14A>G	CUBN	Single nucleotide variant (intron variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 878313	NM_001081.4(CUBN):c.10143C>G (p.Asn3381Lys)	CUBN (N3381K)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299367	NM_001081.4(CUBN):c.10119C>A (p.Val3373=)	CUBN	Single nucleotide variant (synonymous variant)	CUBN-related condition +3 more	GConflicting classifications of pathogenicity
Select item 299368	NM_001081.4(CUBN):c.10102A>G (p.Met3368Val)	CUBN (M3368V)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1 +3 more	GUncertain significance
Select item 299369	NM_001081.4(CUBN):c.10077G>C (p.Ser3359=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome +2 more	GConflicting classifications of pathogenicity
Select item 299370	NM_001081.4(CUBN):c.10076C>T (p.Ser3359Leu)	CUBN (S3359L)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 299371	NM_001081.4(CUBN):c.10039G>A (p.Gly3347Arg)	CUBN (G3347R)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome +1 more	GBenign
Select item 299372	NM_001081.4(CUBN):c.10012C>A (p.Gln3338Lys)	CUBN (Q3338K)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 878894	NM_001081.4(CUBN):c.9990A>C (p.Gln3330His)	CUBN (Q3330H)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 532212	NM_001081.4(CUBN):c.9986C>T (p.Ser3329Leu)	CUBN (S3329L)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 299373	NM_001081.4(CUBN):c.9843A>G (p.Thr3281=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome type 1 +2 more	GBenign
Select item 299374	NM_001081.4(CUBN):c.9714T>C (p.Gly3238=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299375	NM_001081.4(CUBN):c.9664-9T>G	CUBN	Single nucleotide variant (intron variant)	CUBN-related condition +2 more	GConflicting classifications of pathogenicity
Select item 299376	NM_001081.4(CUBN):c.9618G>A (p.Leu3206=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome +1 more	GUncertain significance
Select item 299377	NM_001081.4(CUBN):c.9597C>T (p.Leu3199=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome +1 more	GConflicting classifications of pathogenicity
Select item 299378	NM_001081.4(CUBN):c.9565A>G (p.Ile3189Val)	CUBN (I3189V)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 299379	NM_001081.4(CUBN):c.9525G>A (p.Ser3175=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome type 1 +1 more	GConflicting classifications of pathogenicity
Select item 299380	NM_001081.4(CUBN):c.9491C>G (p.Ser3164Trp)	CUBN (S3164W)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 880121	NM_001081.4(CUBN):c.9442C>T (p.Arg3148Trp)	CUBN (R3148W)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299381	NM_001081.4(CUBN):c.9418G>A (p.Ala3140Thr)	CUBN (A3140T)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 877324	NM_001081.4(CUBN):c.9397A>C (p.Lys3133Gln)	CUBN (K3133Q)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 439584	NM_001081.4(CUBN):c.9340G>A (p.Gly3114Ser)	CUBN (G3114S)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1 +2 more	GBenign/Likely benign
Select item 877325	NM_001081.4(CUBN):c.9335T>C (p.Phe3112Ser)	CUBN (F3112S)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1 +1 more	GConflicting classifications of pathogenicity
Select item 299382	NM_001081.4(CUBN):c.9298G>A (p.Asp3100Asn)	CUBN (D3100N)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 299383	NM_001081.4(CUBN):c.9267C>T (p.Thr3089=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome +1 more	GConflicting classifications of pathogenicity
Select item 877326	NM_001081.4(CUBN):c.9228C>T (p.Ile3076=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 695482	NM_001081.4(CUBN):c.9125A>G (p.Asn3042Ser)	CUBN (N3042S)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome +1 more	GBenign/Likely benign
Select item 522508	NM_001081.4(CUBN):c.9079G>A (p.Gly3027Arg)	CUBN (G3027R)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome +3 more	GConflicting classifications of pathogenicity
Select item 695636	NM_001081.4(CUBN):c.9078C>T (p.Phe3026=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome +2 more	GConflicting classifications of pathogenicity
Select item 299384	NM_001081.4(CUBN):c.9061G>A (p.Glu3021Lys)	CUBN (E3021K)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GConflicting classifications of pathogenicity
Select item 878353	NM_001081.4(CUBN):c.9037G>T (p.Val3013Phe)	CUBN (V3013F)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299385	NM_001081.4(CUBN):c.9036G>A (p.Pro3012=)	CUBN	Single nucleotide variant (synonymous variant)	Imerslund-Grasbeck syndrome type 1	GUncertain significance
Select item 299386	NM_001081.4(CUBN):c.9035C>T (p.Pro3012Leu)	CUBN (P3012L)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance

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