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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2126782	NM_000081.4(LYST):c.11403G>A (p.Gly3801=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 525177	NM_000081.4(LYST):c.11401G>C (p.Gly3801Arg)	LYST (G3801R)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 1656848	NM_000081.4(LYST):c.11400C>T (p.Ala3800=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 968096	NM_000081.4(LYST):c.11393A>G (p.Tyr3798Cys)	LYST (Y3798C)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 2137839	NM_000081.4(LYST):c.11392T>C (p.Tyr3798His)	LYST (Y3798H)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome +1 more	GUncertain significance
Select item 2984169	NM_000081.4(LYST):c.11391C>T (p.Ser3797=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 706164	NM_000081.4(LYST):c.11382C>T (p.Phe3794=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1045854	NM_000081.4(LYST):c.11375A>G (p.Tyr3792Cys)	LYST (Y3792C)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 1046121	NM_000081.4(LYST):c.11368A>G (p.Met3790Val)	LYST (M3790V)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome +1 more	GUncertain significance
Select item 2829723	NM_000081.4(LYST):c.11358G>A (p.Leu3786=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1644773	NM_000081.4(LYST):c.11355C>G (p.Arg3785=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome +1 more	GLikely benign
Select item 451194	NM_000081.4(LYST):c.11354G>A (p.Arg3785His)	LYST (R3785H)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 2706688	NM_000081.4(LYST):c.11349G>A (p.Gln3783=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2806653	NM_000081.4(LYST):c.11346C>T (p.Asp3782=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2704022	NM_000081.4(LYST):c.11346C>A (p.Asp3782Glu)	LYST (D3782E)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 2188609	NM_000081.4(LYST):c.11339G>A (p.Arg3780Gln)	LYST (R3780Q)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 2838220	NM_000081.4(LYST):c.11325G>A (p.Val3775=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 856610	NM_000081.4(LYST):c.11323G>A (p.Val3775Met)	LYST (V3775M)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 1420602	NM_000081.4(LYST):c.11322C>T (p.Thr3774=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1988461	NM_000081.4(LYST):c.11320A>T (p.Thr3774Ser)	LYST (T3774S)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 1985607	NM_000081.4(LYST):c.11312G>A (p.Ser3771Asn)	LYST (S3771N)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 1902693	NM_000081.4(LYST):c.11310C>T (p.Asn3770=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2108479	NM_000081.4(LYST):c.11308A>G (p.Asn3770Asp)	LYST (N3770D)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 1026495	NM_000081.4(LYST):c.11306C>T (p.Ala3769Val)	LYST (A3769V)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 1418793	NM_000081.4(LYST):c.11303C>T (p.Thr3768Ile)	LYST (T3768I)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 1923632	NM_000081.4(LYST):c.11301C>T (p.Tyr3767=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 836271	NM_000081.4(LYST):c.11300A>T (p.Tyr3767Phe)	LYST (Y3767F)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 2756078	NM_000081.4(LYST):c.11289C>G (p.Gly3763=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1582959	NM_000081.4(LYST):c.11289C>T (p.Gly3763=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 570750	NM_000081.4(LYST):c.11278T>C (p.Ser3760Pro)	LYST (S3760P)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 2805926	NM_000081.4(LYST):c.11274A>T (p.Thr3758=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1379183	NM_000081.4(LYST):c.11268C>G (p.Ser3756Arg)	LYST (S3756R)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 296343	NM_000081.4(LYST):c.11268-17dup	LYST	Duplication (intron variant)	Chédiak-Higashi syndrome +1 more	GConflicting classifications of pathogenicity
Select item 403065	NM_000081.4(LYST):c.11268-5del	LYST	Deletion (intron variant)	Chédiak-Higashi syndrome +3 more	GBenign/Likely benign
Select item 296344	NM_000081.4(LYST):c.11268-6_11268-5del	LYST	Deletion (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 2848809	NM_000081.4(LYST):c.11268-9T>C	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2858010	NM_000081.4(LYST):c.11268-11T>A	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2697183	NM_000081.4(LYST):c.11268-13T>C	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2730331	NM_000081.4(LYST):c.11268-15T>C	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2913537	NM_000081.4(LYST):c.11268-17T>C	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1668587	NM_000081.4(LYST):c.11268-17T>A	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 3004827	NM_000081.4(LYST):c.11268-18A>T	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2905345	NM_000081.4(LYST):c.11268-18del	LYST	Deletion (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2857734	NM_000081.4(LYST):c.11267+20T>G	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2795441	NM_000081.4(LYST):c.11267+18del	LYST	Deletion (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2895507	NM_000081.4(LYST):c.11267+17C>A	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2882385	NM_000081.4(LYST):c.11267+17C>G	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1137290	NM_000081.4(LYST):c.11267+17C>T	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2880515	NM_000081.4(LYST):c.11267+13C>T	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2760627	NM_000081.4(LYST):c.11267+12T>G	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2750641	NM_000081.4(LYST):c.11267+10T>C	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1913185	NM_000081.4(LYST):c.11267+3A>G	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 2789072	NM_000081.4(LYST):c.11265C>T (p.Ile3755=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2976910	NM_000081.4(LYST):c.11244C>T (p.Pro3748=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1619962	NM_000081.4(LYST):c.11244C>A (p.Pro3748=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 873776	NM_000081.4(LYST):c.11229A>G (p.Arg3743=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GConflicting classifications of pathogenicity
Select item 2024170	NM_000081.4(LYST):c.11220G>A (p.Lys3740=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1468805	NM_000081.4(LYST):c.11212G>A (p.Asp3738Asn)	LYST (D3738N)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 2150097	NM_000081.4(LYST):c.11196-10dup	LYST	Duplication (intron variant)	Chédiak-Higashi syndrome	GBenign
Select item 2137069	NM_000081.4(LYST):c.11196-9C>G	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2911313	NM_000081.4(LYST):c.11196-10del	LYST	Deletion (intron variant)	Chédiak-Higashi syndrome	GBenign
Select item 2909877	NM_000081.4(LYST):c.11196-10T>C	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2856952	NM_000081.4(LYST):c.11196-17del	LYST	Deletion (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2785056	NM_000081.4(LYST):c.11196-17A>G	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2184552	NM_000081.4(LYST):c.11196-18G>T	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1398626	NM_000081.4(LYST):c.11196-20A>G	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2755499	NM_000081.4(LYST):c.11195+10_11195+16del	LYST	Deletion (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2976255	NM_000081.4(LYST):c.11195+15G>T	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1552667	NM_000081.4(LYST):c.11195+14G>T	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2419017	NM_000081.4(LYST):c.11195+11T>C	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2828441	NM_000081.4(LYST):c.11190T>C (p.Ile3730=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2037027	NM_000081.4(LYST):c.11189T>C (p.Ile3730Thr)	LYST (I3730T)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome +2 more	GUncertain significance
Select item 2794815	NM_000081.4(LYST):c.11187A>C (p.Gly3729=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2196896	NM_000081.4(LYST):c.11168C>T (p.Ala3723Val)	LYST (A3723V)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 296346	NM_000081.4(LYST):c.11167G>A (p.Ala3723Thr)	LYST (A3723T)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 2729096	NM_000081.4(LYST):c.11166C>T (p.Ile3722=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1520138	NM_000081.4(LYST):c.11155A>G (p.Ile3719Val)	LYST (I3719V)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 1573143	NM_000081.4(LYST):c.11151A>G (p.Val3717=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2044626	NM_000081.4(LYST):c.11137C>G (p.Gln3713Glu)	LYST (Q3713E)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 839823	NM_000081.4(LYST):c.11135A>G (p.Asn3712Ser)	LYST (N3712S)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 296347	NM_000081.4(LYST):c.11122G>A (p.Val3708Met)	LYST (V3708M)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome +1 more	GUncertain significance
Select item 2037710	NM_000081.4(LYST):c.11121C>T (p.Ser3707=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1055050	NM_000081.4(LYST):c.11117G>A (p.Cys3706Tyr)	LYST (C3706Y)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 946076	NM_000081.4(LYST):c.11116T>A (p.Cys3706Ser)	LYST (C3706S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2725713	NM_000081.4(LYST):c.11115C>G (p.Ile3705Met)	LYST (I3705M)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 180630	NM_000081.4(LYST):c.11102G>T (p.Cys3701Phe)	LYST (C3701F)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 1304386	NM_000081.4(LYST):c.11101T>G (p.Cys3701Gly)	LYST (C3701G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2048753	NM_000081.4(LYST):c.11094T>C (p.His3698=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 2125496	NM_000081.4(LYST):c.11087T>C (p.Val3696Ala)	LYST (V3696A)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 525196	NM_000081.4(LYST):c.11086G>A (p.Val3696Ile)	LYST (V3696I)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1284627	NM_000081.4(LYST):c.11085C>T (p.Leu3695=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1906444	NM_000081.4(LYST):c.11080G>T (p.Asp3694Tyr)	LYST (D3694Y)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 1055484	NM_000081.4(LYST):c.11079G>T (p.Gly3693=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2088584	NM_000081.4(LYST):c.11077G>A (p.Gly3693Arg)	LYST (G3693R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 296348	NM_000081.4(LYST):c.11076C>T (p.Asn3692=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GConflicting classifications of pathogenicity
Select item 747582	NM_000081.4(LYST):c.11073G>A (p.Val3691=)	LYST	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 936100	NM_000081.4(LYST):c.11070G>A (p.Thr3690=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 1991706	NM_000081.4(LYST):c.11044G>A (p.Gly3682Arg)	LYST (G3682R)	Single nucleotide variant (missense variant)	Chédiak-Higashi syndrome	GUncertain significance
Select item 2747693	NM_000081.4(LYST):c.11043C>T (p.Gly3681=)	LYST	Single nucleotide variant (synonymous variant)	Chédiak-Higashi syndrome	GLikely benign
Select item 2769323	NM_000081.4(LYST):c.11039-11G>C	LYST	Single nucleotide variant (intron variant)	Chédiak-Higashi syndrome	GLikely benign

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