"FMN2-related disorder"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3057805	NM_020066.5(FMN2):c.153G>A (p.Gly51=)	FMN2	Single nucleotide variant (synonymous variant)	FMN2-related disorder	GLikely benign
Select item 3030846	NM_020066.5(FMN2):c.168C>A (p.Gly56=)	FMN2	Single nucleotide variant (synonymous variant)	FMN2-related disorder	GLikely benign
Select item 435214	NM_020066.5(FMN2):c.531G>A (p.Ser177=)	FMN2	Single nucleotide variant (synonymous variant)	FMN2-related disorder +2 more	GBenign/Likely benign
Select item 709718	NM_020066.5(FMN2):c.617AGC[8] (p.Gln212dup)	FMN2	Microsatellite (inframe_insertion)	not provided +1 more	GBenign/Likely benign
Select item 435216	NM_020066.5(FMN2):c.696T>C (p.Pro232=)	FMN2	Single nucleotide variant (synonymous variant)	FMN2-related disorder +2 more	GBenign/Likely benign
Select item 3032065	NM_020066.5(FMN2):c.729C>T (p.Pro243=)	FMN2	Single nucleotide variant (synonymous variant)	FMN2-related disorder	GLikely benign
Select item 2640127	NM_020066.5(FMN2):c.903C>T (p.Val301=)	FMN2	Single nucleotide variant (synonymous variant)	FMN2-related disorder +1 more	GLikely benign
Select item 435219	NM_020066.5(FMN2):c.1259A>C (p.Lys420Thr)	FMN2 (K420T)	Single nucleotide variant (missense variant)	FMN2-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 435220	NM_020066.5(FMN2):c.1352T>A (p.Leu451Gln)	FMN2 (L451Q)	Single nucleotide variant (missense variant)	FMN2-related disorder +2 more	GBenign/Likely benign
Select item 737587	NM_020066.5(FMN2):c.1358G>A (p.Arg453Gln)	FMN2 (R453Q)	Single nucleotide variant (missense variant)	FMN2-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 2388646	NM_020066.5(FMN2):c.1372G>A (p.Ala458Thr)	FMN2 (A458T)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 780811	NM_020066.5(FMN2):c.1782+8G>A	FMN2	Single nucleotide variant (intron variant)	FMN2-related disorder +1 more	GBenign
Select item 740479	NM_020066.5(FMN2):c.1869A>G (p.Pro623=)	FMN2	Single nucleotide variant (synonymous variant)	FMN2-related disorder +1 more	GLikely benign
Select item 435226	NM_020066.5(FMN2):c.1896C>T (p.Pro632=)	FMN2	Single nucleotide variant (synonymous variant)	FMN2-related disorder +2 more	GLikely benign
Select item 3051642	NM_020066.5(FMN2):c.1987-9G>A	FMN2	Single nucleotide variant (intron variant)	FMN2-related disorder	GLikely benign
Select item 3036884	NM_020066.5(FMN2):c.2064C>T (p.Thr688=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3036699	NM_020066.5(FMN2):c.2106A>G (p.Thr702=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3029381	NM_020066.5(FMN2):c.2127A>G (p.Gln709=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3032447	NM_020066.5(FMN2):c.2229G>A (p.Ser743=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3032643	NM_020066.5(FMN2):c.2304A>G (p.Pro768=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3045005	NM_020066.5(FMN2):c.2394C>T (p.Leu798=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3035937	NM_020066.5(FMN2):c.2442A>G (p.Pro814=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3036370	NM_020066.5(FMN2):c.2487G>C (p.Pro829=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 445849	NM_020066.5(FMN2):c.2657T>G (p.Met886Arg)	FMN2 (M890R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 3044686	NM_020066.5(FMN2):c.2730CCCTCC[3] (p.Pro914_Leu915insProPro)	FMN2	Microsatellite (inframe insertion +1 more)	FMN2-related disorder	GLikely benign
Select item 3034861	NM_020066.5(FMN2):c.2736C>T (p.Pro912=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 2640136	NM_020066.5(FMN2):c.2796C>T (p.Leu932=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 3033428	NM_020066.5(FMN2):c.2801_2833del (p.Leu934_Pro944del)	FMN2	Deletion (inframe deletion +1 more)	FMN2-related disorder	GLikely benign
Select item 2640137	NM_020066.5(FMN2):c.2802G>T (p.Leu934=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 3041884	NM_020066.5(FMN2):c.2822G>C (p.Gly941Ala)	FMN2 (G941A +1 more)	Single nucleotide variant (missense variant +1 more)	FMN2-related disorder	GBenign
Select item 3033683	NM_020066.5(FMN2):c.2829_2861del (p.Ala952_Ala962del)	FMN2	Deletion (inframe deletion +1 more)	FMN2-related disorder	GLikely benign
Select item 435227	NM_020066.5(FMN2):c.2823A>C (p.Gly941=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +2 more	GLikely benign
Select item 3056682	NM_020066.5(FMN2):c.2829T>C (p.Pro943=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GBenign
Select item 218765	NM_020066.5(FMN2):c.2840C>T (p.Pro947Leu)	FMN2 (P951L +1 more)	Single nucleotide variant (missense variant +1 more)	FMN2-related disorder +2 more	GBenign/Likely benign
Select item 3042195	NM_020066.5(FMN2):c.2844A>T (p.Leu948=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GBenign
Select item 3041627	NM_020066.5(FMN2):c.2850A>G (p.Gly950=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GBenign
Select item 3042171	NM_020066.5(FMN2):c.2852_2853insA (p.Ala952fs)	FMN2 (A952fs +1 more)	Insertion (frameshift variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3039868	NM_020066.5(FMN2):c.2853G>A (p.Ala951=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3041724	NM_020066.5(FMN2):c.2857del (p.Ile953fs)	FMN2 (I953fs +1 more)	Deletion (frameshift variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3040395	NM_020066.5(FMN2):c.2862C>T (p.Pro954=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3041558	NM_020066.5(FMN2):c.2868G>T (p.Pro956=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GBenign
Select item 3040681	NM_020066.5(FMN2):c.2868G>A (p.Pro956=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3036961	NM_020066.5(FMN2):c.2871C>T (p.Pro957=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 2640140	NM_020066.5(FMN2):c.2874T>A (p.Pro958=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 3038926	NM_020066.5(FMN2):c.2877T>A (p.Leu959=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3041290	NM_020066.5(FMN2):c.2883G>A (p.Gly961=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 435228	NM_020066.5(FMN2):c.2886A>G (p.Ala962=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +2 more	GLikely benign
Select item 218766	NM_020066.5(FMN2):c.2897T>C (p.Leu966Pro)	FMN2 (L970P +1 more)	Single nucleotide variant (missense variant +1 more)	FMN2-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 2640141	NM_020066.5(FMN2):c.2901T>G (p.Pro967=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 3060923	NM_020066.5(FMN2):c.2907T>A (p.Pro969=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3056382	NM_020066.5(FMN2):c.2916A>G (p.Gly972=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GBenign
Select item 3037308	NM_020066.5(FMN2):c.2919A>G (p.Ala973=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GBenign
Select item 3032450	NM_020066.5(FMN2):c.2928T>A (p.Pro976=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 1675410	NM_020066.5(FMN2):c.2928T>C (p.Pro976=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 1675411	NM_020066.5(FMN2):c.2934A>T (p.Pro978=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2640143	NM_020066.5(FMN2):c.2937C>G (p.Pro979=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +2 more	GLikely benign
Select item 2640149	NM_020066.5(FMN2):c.2967T>A (p.Pro989=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 2570757	NM_020066.5(FMN2):c.2979C>T (p.Pro993=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 3036377	NM_020066.5(FMN2):c.2997T>A (p.Pro999=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3056508	NM_020066.5(FMN2):c.3000G>T (p.Pro1000=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GBenign
Select item 2640152	NM_020066.5(FMN2):c.3003C>G (p.Pro1001=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 2640153	NM_020066.5(FMN2):c.3015A>G (p.Gly1005=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 3036846	NM_020066.5(FMN2):c.3021C>A (p.Gly1007=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3057646	NM_020066.5(FMN2):c.3029C>T (p.Pro1010Leu)	FMN2 (P1010L +1 more)	Single nucleotide variant (missense variant +1 more)	FMN2-related disorder	GLikely benign
Select item 2640155	NM_020066.5(FMN2):c.3033T>G (p.Pro1011=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 2640156	NM_020066.5(FMN2):c.3036C>G (p.Pro1012=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 3043162	NM_020066.5(FMN2):c.3042T>A (p.Leu1014=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3036746	NM_020066.5(FMN2):c.3048A>G (p.Gly1016=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 2640157	NM_020066.5(FMN2):c.3060T>C (p.Pro1020=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 3041252	NM_020066.5(FMN2):c.3066A>T (p.Pro1022=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 2640158	NM_020066.5(FMN2):c.3066A>G (p.Pro1022=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 2640159	NM_020066.5(FMN2):c.3072T>A (p.Pro1024=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 3039785	NM_020066.5(FMN2):c.3099G>T (p.Pro1033=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3051656	NM_020066.5(FMN2):c.3111C>T (p.Pro1037=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3045185	NM_020066.5(FMN2):c.3120C>A (p.Gly1040=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 2640164	NM_020066.5(FMN2):c.3126C>T (p.Pro1042=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 2570758	NM_020066.5(FMN2):c.3132G>T (p.Pro1044=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2640167	NM_020066.5(FMN2):c.3138A>T (p.Pro1046=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 3029532	NM_020066.5(FMN2):c.3144C>T (p.Pro1048=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 2640170	NM_020066.5(FMN2):c.3165T>G (p.Pro1055=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 435229	NM_020066.5(FMN2):c.3174T>A (p.Leu1058=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +2 more	GLikely benign
Select item 871332	NM_020066.5(FMN2):c.3186C>A (p.Gly1062=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2498451	NM_020066.5(FMN2):c.3192T>C (p.Pro1064=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3031457	NM_020066.5(FMN2):c.3204T>A (p.Pro1068=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 2640173	NM_020066.5(FMN2):c.3207A>T (p.Leu1069=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 2640175	NM_020066.5(FMN2):c.3231G>T (p.Pro1077=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 3045542	NM_020066.5(FMN2):c.3234C>T (p.Pro1078=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3052114	NM_020066.5(FMN2):c.3237A>T (p.Pro1079=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3031440	NM_020066.5(FMN2):c.3240T>A (p.Leu1080=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 1879123	NM_020066.5(FMN2):c.3276C>T (p.Pro1092=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3040702	NM_020066.5(FMN2):c.3291C>G (p.Pro1097=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 3040499	NM_020066.5(FMN2):c.3291C>T (p.Pro1097=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder	GLikely benign
Select item 2640179	NM_020066.5(FMN2):c.3294T>A (p.Pro1098=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 2640180	NM_020066.5(FMN2):c.3297G>A (p.Pro1099=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	FMN2-related disorder +1 more	GLikely benign
Select item 1335023	NM_020066.5(FMN2):c.3297G>T (p.Pro1099=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2582877	NM_020066.5(FMN2):c.3306A>T (p.Leu1102=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3042118	NM_020066.5(FMN2):c.3314T>C (p.Val1105Ala)	FMN2 (V1105A +1 more)	Single nucleotide variant (missense variant +1 more)	FMN2-related disorder	GBenign
Select item 1694551	NM_020066.5(FMN2):c.3324TCC[1] (p.Pro1112del)	FMN2 (P1112del +1 more)	Microsatellite (inframe_deletion +1 more)	FMN2-related disorder +2 more	GBenign/Likely benign
Select item 1298466	NM_020066.5(FMN2):c.3324T>C (p.Pro1108=)	FMN2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2640184	NM_020066.5(FMN2):c.3339ACCCGGAGCGGGCATACCCCCTCCTCCCCCTCT[1] (p.1115GAGIPPPPPLP[2])	FMN2	Microsatellite (inframe_deletion +1 more)	FMN2-related disorder +1 more	GBenign/Likely benign

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