C3280215[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 303372	NM_001378964.1(CDON):c.*4097A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303373	NM_001378964.1(CDON):c.*4080G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 878586	NM_001378964.1(CDON):c.*4063G>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303374	NM_001378964.1(CDON):c.*4052C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 878587	NM_001378964.1(CDON):c.*4007G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 878588	NM_001378964.1(CDON):c.*4000C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303375	NM_001378964.1(CDON):c.*3972C>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GLikely benign
Select item 879178	NM_001378964.1(CDON):c.*3971G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303376	NM_001378964.1(CDON):c.*3919T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GLikely benign
Select item 303377	NM_001378964.1(CDON):c.*3916G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303378	NM_001378964.1(CDON):c.*3884T>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303379	NM_001378964.1(CDON):c.*3862G>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303380	NM_001378964.1(CDON):c.*3830G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 879179	NM_001378964.1(CDON):c.*3777G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303381	NM_001378964.1(CDON):c.*3765C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 880383	NM_001378964.1(CDON):c.*3655T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303382	NM_001378964.1(CDON):c.*3628C>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303383	NM_001378964.1(CDON):c.*3610C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 880384	NM_001378964.1(CDON):c.*3514A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303385	NM_001378964.1(CDON):c.*3490T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303386	NM_001378964.1(CDON):c.*3481C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303387	NM_001378964.1(CDON):c.*3424T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303388	NM_001378964.1(CDON):c.*3409T>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 877614	NM_001378964.1(CDON):c.*3294A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 877615	NM_001378964.1(CDON):c.*3269G>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 877616	NM_001378964.1(CDON):c.*3235G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303389	NM_001378964.1(CDON):c.*3221A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GLikely benign
Select item 303390	NM_001378964.1(CDON):c.*3210A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303391	NM_001378964.1(CDON):c.*3176C>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GLikely benign
Select item 303392	NM_001378964.1(CDON):c.*3141A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11 +1 more	GBenign/Likely benign
Select item 303393	NM_001378964.1(CDON):c.*3133A>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303394	NM_001378964.1(CDON):c.*3104T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303395	NM_001378964.1(CDON):c.*3076T>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 878629	NM_001378964.1(CDON):c.*3060C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 878630	NM_001378964.1(CDON):c.*2999C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303396	NM_001378964.1(CDON):c.*2992T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 878631	NM_001378964.1(CDON):c.*2933C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 878632	NM_001378964.1(CDON):c.*2847G>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303397	NM_001378964.1(CDON):c.*2830A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303398	NM_001378964.1(CDON):c.*2769G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 879228	NM_001378964.1(CDON):c.*2760A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 879229	NM_001378964.1(CDON):c.*2755A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303399	NM_001378964.1(CDON):c.*2749C>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11 +1 more	GBenign
Select item 303400	NM_001378964.1(CDON):c.*2740T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303401	NM_001378964.1(CDON):c.*2734G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 880422	NM_001378964.1(CDON):c.*2730A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303402	NM_001378964.1(CDON):c.*2717C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303403	NM_001378964.1(CDON):c.*2705C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303404	NM_001378964.1(CDON):c.*2698T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303405	NM_001378964.1(CDON):c.*2640A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303406	NM_001378964.1(CDON):c.*2580G>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303407	NM_001378964.1(CDON):c.*2573G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303420	NM_001378964.1(CDON):c.*2379T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303437	NM_001378964.1(CDON):c.*2377T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 877663	NM_001378964.1(CDON):c.*2375C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303439	NM_001378964.1(CDON):c.*2373C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 877664	NM_001378964.1(CDON):c.*2349A>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 877665	NM_001378964.1(CDON):c.*2347T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 877666	NM_001378964.1(CDON):c.*2345T>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 877667	NM_001378964.1(CDON):c.*2339T>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303443	NM_001378964.1(CDON):c.*2291T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303445	NM_001378964.1(CDON):c.*2264C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303446	NM_001378964.1(CDON):c.*2195G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303447	NM_001378964.1(CDON):c.*2101A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303448	NM_001378964.1(CDON):c.*2097G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 878678	NM_001378964.1(CDON):c.*2057G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 878679	NM_001378964.1(CDON):c.*2024C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303449	NM_001378964.1(CDON):c.*2003C>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303450	NM_001378964.1(CDON):c.*1933A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 879284	NM_001378964.1(CDON):c.*1874G>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 879285	NM_001378964.1(CDON):c.*1834G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303451	NM_001378964.1(CDON):c.*1816C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 879286	NM_001378964.1(CDON):c.*1805A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303452	NM_001378964.1(CDON):c.*1803C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303453	NM_001378964.1(CDON):c.*1800A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303454	NM_001378964.1(CDON):c.*1745A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303455	NM_001378964.1(CDON):c.*1736C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 880465	NM_001378964.1(CDON):c.*1671G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303456	NM_001378964.1(CDON):c.*1661C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303457	NM_001378964.1(CDON):c.*1589G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303458	NM_001378964.1(CDON):c.*1572A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303459	NM_001378964.1(CDON):c.*1517G>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 880466	NM_001378964.1(CDON):c.*1457G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GLikely benign
Select item 303462	NM_001378964.1(CDON):c.*1429C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303463	NM_001378964.1(CDON):c.*1332T>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303464	NM_001378964.1(CDON):c.*1327T>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303467	NM_001378964.1(CDON):c.*1307T>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303468	NM_001378964.1(CDON):c.*1216G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303469	NM_001378964.1(CDON):c.*1211A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303470	NM_001378964.1(CDON):c.*1151C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 877701	NM_001378964.1(CDON):c.*1062C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance
Select item 303471	NM_001378964.1(CDON):c.*1061T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303472	NM_001378964.1(CDON):c.*1016C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303473	NM_001378964.1(CDON):c.*983A>G	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303474	NM_001378964.1(CDON):c.*916G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303475	NM_001378964.1(CDON):c.*911T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303476	NM_001378964.1(CDON):c.*897T>C	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303477	NM_001378964.1(CDON):c.*871C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303478	NM_001378964.1(CDON):c.*864G>A	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GBenign
Select item 303479	NM_001378964.1(CDON):c.*863C>T	CDON	Single nucleotide variant (3 prime UTR variant)	Holoprosencephaly 11	GUncertain significance

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