ClinVar for Gene (Select 3579) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3270417	NM_001557.4(CXCR2):c.892G>A (p.Ala298Thr)	CXCR2 (A298T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270415	NM_001557.4(CXCR2):c.745G>T (p.Ala249Ser)	CXCR2 (A249S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270414	NM_001557.4(CXCR2):c.824C>A (p.Thr275Asn)	CXCR2 (T275N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270413	NM_001557.4(CXCR2):c.898G>A (p.Glu300Lys)	CXCR2 (E300K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3148939	GRCh37/hg19 2q35-37.3(chr2:216815496-242782258)x3	AAMP, ABCB6 +218 more	Copy number gain	See cases	GPathogenic
Select item 3079202	NM_001557.4(CXCR2):c.569C>T (p.Ser190Phe)	CXCR2 (S190F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079201	NM_001557.4(CXCR2):c.458G>C (p.Arg153Pro)	CXCR2 (R153P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3029142	NM_001557.4(CXCR2):c.654T>C (p.Phe218=)	CXCR2	Single nucleotide variant (synonymous variant)	CXCR2-related disorder	GLikely benign
Select item 3010091	NM_001557.4(CXCR2):c.625A>G (p.Met209Val)	CXCR2 (M209V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3006015	NM_001557.4(CXCR2):c.870T>C (p.Asn290=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3004731	NM_001557.4(CXCR2):c.27C>T (p.Asp9=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 3004621	NM_001557.4(CXCR2):c.336G>T (p.Trp112Cys)	CXCR2 (W112C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2997916	NM_001557.4(CXCR2):c.272C>T (p.Ala91Val)	CXCR2 (A91V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2989732	NM_001557.4(CXCR2):c.190C>A (p.Leu64Met)	CXCR2 (L64M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2989693	NM_001557.4(CXCR2):c.549C>T (p.Phe183=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2974950	NM_001557.4(CXCR2):c.75C>T (p.Tyr25=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2972803	NM_001557.4(CXCR2):c.140A>G (p.Asn47Ser)	CXCR2 (N47S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2972656	NM_001557.4(CXCR2):c.930C>T (p.Asn310=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2962869	NM_001557.4(CXCR2):c.243C>T (p.Ser81=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2961853	NM_001557.4(CXCR2):c.408_409inv (p.Leu136_Leu137=)	CXCR2	Inversion (synonymous variant)	not provided	GUncertain significance
Select item 2907002	NM_001557.4(CXCR2):c.880C>T (p.Arg294Trp)	CXCR2 (R294W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2890443	NM_001557.4(CXCR2):c.642G>T (p.Leu214=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2882006	NM_001557.4(CXCR2):c.78C>T (p.Ser26=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2869654	NM_001557.4(CXCR2):c.1062G>A (p.Gly354=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2869502	NM_001557.4(CXCR2):c.694G>A (p.Gly232Arg)	CXCR2 (G232R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2868957	NM_001557.4(CXCR2):c.114A>G (p.Pro38=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2867145	NM_001557.4(CXCR2):c.512G>A (p.Gly171Asp)	CXCR2 (G171D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2860982	NM_001557.4(CXCR2):c.221T>C (p.Leu74Ser)	CXCR2 (L74S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2860307	NM_001557.4(CXCR2):c.681G>A (p.Met227Ile)	CXCR2 (M227I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2855124	NM_001557.4(CXCR2):c.910A>G (p.Ile304Val)	CXCR2 (I304V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2835873	NM_001557.4(CXCR2):c.1057T>C (p.Ser353Pro)	CXCR2 (S353P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2830239	NM_001557.4(CXCR2):c.779T>C (p.Phe260Ser)	CXCR2 (F260S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2821307	NM_001557.4(CXCR2):c.232G>A (p.Val78Ile)	CXCR2 (V78I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2812213	NM_001557.4(CXCR2):c.597C>T (p.Asp199=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2810578	NM_001557.4(CXCR2):c.644C>G (p.Pro215Arg)	CXCR2 (P215R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2807003	NM_001557.4(CXCR2):c.534G>C (p.Leu178=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2806952	NM_001557.4(CXCR2):c.243C>A (p.Ser81=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2806228	NM_001557.4(CXCR2):c.306del (p.Ile103fs)	CXCR2 (I103fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2788962	NM_001557.4(CXCR2):c.300C>T (p.Thr100=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2788188	NM_001557.4(CXCR2):c.630G>A (p.Leu210=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2780606	NM_001557.4(CXCR2):c.903T>C (p.Ile301=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2779339	NM_001557.4(CXCR2):c.619T>A (p.Trp207Arg)	CXCR2 (W207R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2772713	NM_001557.4(CXCR2):c.663C>A (p.Ile221=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2771644	NM_001557.4(CXCR2):c.294C>T (p.Ala98=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2748344	NM_001557.4(CXCR2):c.624G>A (p.Arg208=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2693810	NM_001557.4(CXCR2):c.877G>A (p.Asp293Asn)	CXCR2 (D293N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2685875	GRCh37/hg19 2q35-37.3(chr2:218376403-242783384)x3	AAMP, ABCB6 +208 more	Copy number gain	not provided	GPathogenic
Select item 2605526	NM_001557.4(CXCR2):c.1046T>G (p.Val349Gly)	CXCR2 (V349G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2580353	GRCh37/hg19 2q32.1-36.1(chr2:186698504-223918111)x3	AAMP, ABCA12 +208 more	Copy number gain	See cases	GPathogenic
Select item 2531288	NM_001557.4(CXCR2):c.1015T>A (p.Ser339Thr)	CXCR2 (S339T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529963	NM_001557.4(CXCR2):c.386A>G (p.Asn129Ser)	CXCR2 (N129S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487595	NM_001557.4(CXCR2):c.992T>C (p.Ile331Thr)	CXCR2 (I331T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2474530	NM_001557.4(CXCR2):c.228C>G (p.Ser76Arg)	CXCR2 (S76R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393318	NM_001557.4(CXCR2):c.148T>C (p.Phe50Leu)	CXCR2 (F50L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340073	NM_001557.4(CXCR2):c.281A>G (p.Asp94Gly)	CXCR2 (D94G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321722	NM_001557.4(CXCR2):c.524T>A (p.Leu175His)	CXCR2 (L175H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318622	NM_001557.4(CXCR2):c.416G>A (p.Cys139Tyr)	CXCR2 (C139Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267647	NM_001557.4(CXCR2):c.913C>G (p.Leu305Val)	CXCR2 (L305V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222333	NM_001557.4(CXCR2):c.611C>T (p.Thr204Ile)	CXCR2 (T204I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2200001	NM_001557.4(CXCR2):c.475C>T (p.Arg159Cys)	CXCR2 (R159C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2191889	NM_001557.4(CXCR2):c.591T>C (p.Tyr197=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2187989	NM_001557.4(CXCR2):c.316G>A (p.Ala106Thr)	CXCR2 (A106T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2180050	NM_001557.4(CXCR2):c.204C>G (p.Leu68=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2178469	NM_001557.4(CXCR2):c.942C>T (p.Tyr314=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2176652	NM_001557.4(CXCR2):c.315C>T (p.Ala105=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2164631	NM_001557.4(CXCR2):c.664G>A (p.Val222Met)	CXCR2 (V222M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2163343	NM_001557.4(CXCR2):c.727A>G (p.Met243Val)	CXCR2 (M243V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2160579	NM_001557.4(CXCR2):c.710C>T (p.Thr237Met)	CXCR2 (T237M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2154040	NM_001557.4(CXCR2):c.1043T>C (p.Phe348Ser)	CXCR2 (F348S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2128217	NM_001557.4(CXCR2):c.453C>T (p.Ala151=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2114565	NM_001557.4(CXCR2):c.504C>T (p.Ser168=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2097921	NM_001557.4(CXCR2):c.829A>T (p.Met277Leu)	CXCR2 (M277L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2074050	NM_001557.4(CXCR2):c.334T>C (p.Trp112Arg)	CXCR2 (W112R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2062630	NM_001557.4(CXCR2):c.1080C>A (p.Leu360=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2059374	NM_001557.4(CXCR2):c.43T>C (p.Trp15Arg)	CXCR2 (W15R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2056380	NM_001557.4(CXCR2):c.1021C>A (p.Pro341Thr)	CXCR2 (P341T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2051276	NM_001557.4(CXCR2):c.482T>G (p.Leu161Trp)	CXCR2 (L161W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2050538	NM_001557.4(CXCR2):c.32T>C (p.Phe11Ser)	CXCR2 (F11S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2043647	NM_001557.4(CXCR2):c.972A>C (p.Gly324=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2041951	NM_001557.4(CXCR2):c.1021C>T (p.Pro341Ser)	CXCR2 (P341S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2040462	NM_001557.4(CXCR2):c.856T>G (p.Cys286Gly)	CXCR2 (C286G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2029134	NM_001557.4(CXCR2):c.882G>A (p.Arg294=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2026251	NM_001557.4(CXCR2):c.1047T>G (p.Val349=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2025623	NM_001557.4(CXCR2):c.945C>T (p.Ala315=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2000526	NM_001557.4(CXCR2):c.1041del (p.Phe348fs)	CXCR2 (F348fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2000471	NM_001557.4(CXCR2):c.67T>G (p.Tyr23Asp)	CXCR2 (Y23D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1999022	NM_001557.4(CXCR2):c.189G>C (p.Leu63=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1992670	NM_001557.4(CXCR2):c.94T>G (p.Phe32Val)	CXCR2 (F32V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1981881	NM_001557.4(CXCR2):c.559G>A (p.Val187Ile)	CXCR2 (V187I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1981146	NM_001557.4(CXCR2):c.849G>A (p.Gln283=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1979261	NM_001557.4(CXCR2):c.430C>T (p.Arg144Cys)	CXCR2 (R144C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1974177	NM_001557.4(CXCR2):c.153G>C (p.Val51=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1967499	NM_001557.4(CXCR2):c.185G>A (p.Ser62Asn)	CXCR2 (S62N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1961608	NM_001557.4(CXCR2):c.223T>C (p.Tyr75His)	CXCR2 (Y75H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1961192	NM_001557.4(CXCR2):c.394A>C (p.Ser132Arg)	CXCR2 (S132R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1950651	NM_001557.4(CXCR2):c.271G>A (p.Ala91Thr)	CXCR2 (A91T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1944401	NM_001557.4(CXCR2):c.172G>A (p.Val58Ile)	CXCR2 (V58I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1942132	NM_001557.4(CXCR2):c.684G>A (p.Leu228=)	CXCR2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1935259	NM_001557.4(CXCR2):c.982A>G (p.Ile328Val)	CXCR2 (I328V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1933615	NM_001557.4(CXCR2):c.965G>A (p.Arg322His)	CXCR2 (R322H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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