"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "CNOT1"[ - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1974209	NM_016284.5(CNOT1):c.7089G>A (p.Gln2363=)	CNOT1, SETD6	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2191274	NM_016284.5(CNOT1):c.7068C>T (p.Val2356=)	CNOT1, SETD6	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 1973114	NM_016284.5(CNOT1):c.7047C>T (p.Ile2349=)	CNOT1, SETD6	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2758049	NM_016284.5(CNOT1):c.7020T>A (p.His2340Gln)	CNOT1, SETD6 (H2335Q +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2065312	NM_016284.5(CNOT1):c.7008G>A (p.Lys2336=)	CNOT1, SETD6	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2028858	NM_016284.5(CNOT1):c.6918-16T>G	CNOT1, SETD6	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2070562	NM_016284.5(CNOT1):c.6917+7G>A	CNOT1, SETD6	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2176286	NM_016284.5(CNOT1):c.6891G>C (p.Thr2297=)	CNOT1, SETD6	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2040651	NM_016284.5(CNOT1):c.6852C>T (p.Phe2284=)	CNOT1, SETD6	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 1569231	NM_016284.5(CNOT1):c.6849C>T (p.Tyr2283=)	CNOT1, SETD6	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 3017281	NM_016284.5(CNOT1):c.6791A>C (p.Tyr2264Ser)	CNOT1, SETD6 (Y2264S +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2104185	NM_016284.5(CNOT1):c.6785-8del	CNOT1, SETD6	Deletion (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1971099	NM_016284.5(CNOT1):c.6784+11C>T	CNOT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2001866	NM_016284.5(CNOT1):c.6781G>A (p.Glu2261Lys)	CNOT1 (E2261K +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2107828	NM_016284.5(CNOT1):c.6705C>T (p.Ser2235=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2174122	NM_016284.5(CNOT1):c.6683C>T (p.Ala2228Val)	CNOT1 (A2223V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2114188	NM_016284.5(CNOT1):c.6675G>A (p.Gln2225=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2780547	NM_016284.5(CNOT1):c.6632A>G (p.Asn2211Ser)	CNOT1 (N2206S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2041463	NM_016284.5(CNOT1):c.6611A>G (p.Asn2204Ser)	CNOT1 (N2199S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1973482	NM_016284.5(CNOT1):c.6603+18A>C	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2106020	NM_016284.5(CNOT1):c.6603+17T>A	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2722914	NM_016284.5(CNOT1):c.6576C>T (p.Phe2192=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2102086	NM_016284.5(CNOT1):c.6549T>C (p.Tyr2183=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2733853	NM_016284.5(CNOT1):c.6546C>T (p.Ser2182=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2065708	NM_016284.5(CNOT1):c.6525G>A (p.Gln2175=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1998064	NM_016284.5(CNOT1):c.6467G>A (p.Ser2156Asn)	CNOT1 (S2151N +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2695496	NM_016284.5(CNOT1):c.6454-9C>G	CNOT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1971501	NM_016284.5(CNOT1):c.6453+19A>T	CNOT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1972109	NM_016284.5(CNOT1):c.6453+12A>G	CNOT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2646572	NM_016284.5(CNOT1):c.6429C>T (p.Pro2143=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2038059	NM_016284.5(CNOT1):c.6422G>A (p.Arg2141Lys)	CNOT1 (R2136K +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2413974	NM_016284.5(CNOT1):c.6405C>T (p.Ala2135=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2695497	NM_016284.5(CNOT1):c.6381G>A (p.Gln2127=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1972303	NM_016284.5(CNOT1):c.6279+19T>C	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1975690	NM_016284.5(CNOT1):c.6279+11del	CNOT1	Deletion (intron variant)	not provided	GLikely benign
Select item 2049072	NM_016284.5(CNOT1):c.6228G>A (p.Ala2076=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2083907	NM_016284.5(CNOT1):c.6178-14TTTC[2]	CNOT1	Microsatellite (intron variant)	not provided	GLikely benign
Select item 1992687	NM_016284.5(CNOT1):c.6178-7C>T	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2108002	NM_016284.5(CNOT1):c.6178-11C>A	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1974425	NM_016284.5(CNOT1):c.6178-16C>T	CNOT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2025890	NM_016284.5(CNOT1):c.6178-17A>G	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2045542	NM_016284.5(CNOT1):c.6177+11A>G	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2008424	NM_016284.5(CNOT1):c.6177+8T>G	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2880440	NM_016284.5(CNOT1):c.6168A>G (p.Pro2056=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1906836	NM_016284.5(CNOT1):c.6165G>C (p.Thr2055=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2752089	NM_016284.5(CNOT1):c.6115C>A (p.Leu2039Ile)	CNOT1 (L2034I +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1895722	NM_016284.5(CNOT1):c.6111C>T (p.Ala2037=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1658832	NM_016284.5(CNOT1):c.6059+17C>T	CNOT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1974211	NM_016284.5(CNOT1):c.6059+8T>C	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1928202	NM_016284.5(CNOT1):c.6006T>C (p.Asn2002=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2804636	NM_016284.5(CNOT1):c.5898C>T (p.Val1966=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1217372	NM_016284.5(CNOT1):c.5896-5C>T	CNOT1	Single nucleotide variant (intron variant)	Holoprosencephaly 12 with or without pancreatic agenesis +2 more	GBenign
Select item 1976063	NM_016284.5(CNOT1):c.5896-16T>C	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2752001	NM_016284.5(CNOT1):c.5895+14del	CNOT1	Deletion (intron variant)	not provided	GLikely benign
Select item 2064548	NM_016284.5(CNOT1):c.5895+9T>C	CNOT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2014334	NM_016284.5(CNOT1):c.5895+4T>C	CNOT1	Single nucleotide variant (intron variant)	not provided +1 more	GUncertain significance
Select item 2186566	NM_016284.5(CNOT1):c.5887C>T (p.Leu1963=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2100244	NM_016284.5(CNOT1):c.5847C>T (p.His1949=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2008613	NM_016284.5(CNOT1):c.5838C>T (p.Leu1946=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 786944	NM_016284.5(CNOT1):c.5829T>C (p.Ile1943=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2898346	NM_016284.5(CNOT1):c.5727C>T (p.Ile1909=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2810102	NM_016284.5(CNOT1):c.5705G>T (p.Cys1902Phe)	CNOT1 (C1902F +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2060061	NM_016284.5(CNOT1):c.5673C>T (p.Thr1891=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2780154	NM_016284.5(CNOT1):c.5647-19T>C	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2189249	NM_016284.5(CNOT1):c.5610C>T (p.Arg1870=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2898347	NM_016284.5(CNOT1):c.5607C>T (p.Gly1869=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1976793	NM_016284.5(CNOT1):c.5574A>G (p.Glu1858=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2104525	NM_016284.5(CNOT1):c.5556A>G (p.Ala1852=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2034769	NM_016284.5(CNOT1):c.5415-8T>C	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2707705	NM_016284.5(CNOT1):c.5415-14A>G	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1999062	NM_016284.5(CNOT1):c.5368A>G (p.Thr1790Ala)	CNOT1 (T1785A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2875149	NM_016284.5(CNOT1):c.5332C>T (p.His1778Tyr)	CNOT1 (H1773Y +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1971376	NM_016284.5(CNOT1):c.5244+20G>T	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1978331	NM_016284.5(CNOT1):c.5241G>A (p.Ala1747=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2129287	NM_016284.5(CNOT1):c.5211T>G (p.Val1737=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2756633	NM_016284.5(CNOT1):c.5182G>A (p.Val1728Met)	CNOT1 (V1723M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2100051	NM_016284.5(CNOT1):c.5144T>C (p.Ile1715Thr)	CNOT1 (I1715T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2000489	NM_016284.5(CNOT1):c.5136-15T>C	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1974900	NM_016284.5(CNOT1):c.5135+16C>T	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2713743	NM_016284.5(CNOT1):c.5107T>G (p.Ser1703Ala)	CNOT1 (S1703A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2162821	NM_016284.5(CNOT1):c.5106G>A (p.Gly1702=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2096164	NM_016284.5(CNOT1):c.5058A>G (p.Glu1686=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2416548	NM_016284.5(CNOT1):c.5040T>G (p.Leu1680=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 2020784	NM_016284.5(CNOT1):c.5012A>T (p.Asp1671Val)	CNOT1 (D1671V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1976537	NM_016284.5(CNOT1):c.4993-18G>A	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1972925	NM_016284.5(CNOT1):c.4993-19C>T	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1973756	NM_016284.5(CNOT1):c.4992+16A>G	CNOT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2099867	NM_016284.5(CNOT1):c.4944A>T (p.Leu1648Phe)	CNOT1 (L1643F +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1976916	NM_016284.5(CNOT1):c.4893C>T (p.Ala1631=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2077579	NM_016284.5(CNOT1):c.4874C>G (p.Ala1625Gly)	CNOT1 (A1620G +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2060102	NM_016284.5(CNOT1):c.4857G>A (p.Leu1619=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2804996	NM_016284.5(CNOT1):c.4800+8T>G	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2973502	NM_016284.5(CNOT1):c.4788C>T (p.Ala1596=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1971325	NM_016284.5(CNOT1):c.4734T>C (p.Asn1578=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1217373	NM_016284.5(CNOT1):c.4716C>T (p.Tyr1572=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	Holoprosencephaly 12 with or without pancreatic agenesis +2 more	GBenign
Select item 2068515	NM_016284.5(CNOT1):c.4686T>C (p.Gly1562=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2719167	NM_016284.5(CNOT1):c.4680+16C>G	CNOT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2048418	NM_016284.5(CNOT1):c.4680+8T>C	CNOT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2192593	NM_016284.5(CNOT1):c.4662A>G (p.Pro1554=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2417960	NM_016284.5(CNOT1):c.4656G>A (p.Arg1552=)	CNOT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

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