ClinVar for Gene (Select 2147) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063941	NM_000506.5(F2):c.65_69dup	F2	Duplication (3 prime UTR variant)	not specified	GUncertain significance
Select item 3023610	NM_000506.5(F2):c.1668T>C (p.Asp556=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 3022128	NM_000506.5(F2):c.1251C>T (p.Phe417=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 3015914	NM_000506.5(F2):c.1678C>T (p.Arg560Ter)	F2 (R560*)	Single nucleotide variant (nonsense)	Congenital prothrombin deficiency	GPathogenic
Select item 3014060	NM_000506.5(F2):c.1704T>C (p.Ser568=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 3013784	NM_000506.5(F2):c.135C>T (p.Asn45=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2989623	NM_000506.5(F2):c.1726-11TTC[2]	F2	Microsatellite (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2985454	NM_000506.5(F2):c.423-4C>G	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2983678	NM_000506.5(F2):c.1473-8C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2974142	NM_000506.5(F2):c.948C>A (p.Ala316=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2971116	NM_000506.5(F2):c.240+7C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2970823	NM_000506.5(F2):c.1362C>T (p.Asn454=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2966946	NM_000506.5(F2):c.954dup (p.Glu319Ter)	F2 (E319*)	Duplication (nonsense)	Congenital prothrombin deficiency	GPathogenic
Select item 2963250	NM_000506.5(F2):c.1131-9C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2962433	NM_000506.5(F2):c.327T>C (p.Ala109=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2958931	NM_000506.5(F2):c.1224C>T (p.Leu408=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2957927	NM_000506.5(F2):c.349C>T (p.Arg117Ter)	F2 (R117*)	Single nucleotide variant (nonsense)	Congenital prothrombin deficiency	GPathogenic
Select item 2955966	NM_000506.5(F2):c.1434T>C (p.Ile478=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2955063	NM_000506.5(F2):c.369C>T (p.Thr123=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2920253	NM_000506.5(F2):c.1277T>C (p.Ile426Thr)	F2 (I426T)	Single nucleotide variant (missense variant)	Congenital prothrombin deficiency	GUncertain significance
Select item 2919768	NM_000506.5(F2):c.192G>A (p.Thr64=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2917355	NM_000506.5(F2):c.1026C>T (p.Phe342=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2916209	NM_000506.5(F2):c.1530G>A (p.Thr510=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2914787	NM_000506.5(F2):c.317-5C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2909585	NM_000506.5(F2):c.843C>A (p.Gly281=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2908902	NM_000506.5(F2):c.870T>C (p.Tyr290=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2907919	NM_000506.5(F2):c.393A>G (p.Leu131=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2907841	NM_000506.5(F2):c.192G>C (p.Thr64=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2907385	NM_000506.5(F2):c.6G>A (p.Ala2=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2906676	NM_000506.5(F2):c.1351C>A (p.Pro451Thr)	F2 (P451T)	Single nucleotide variant (missense variant)	Congenital prothrombin deficiency	GUncertain significance
Select item 2905159	NM_000506.5(F2):c.321C>T (p.Asn107=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2904773	NM_000506.5(F2):c.1225C>T (p.Leu409=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2903973	NM_000506.5(F2):c.762T>C (p.Ala254=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2903521	NM_000506.5(F2):c.1473-20C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2902367	NM_000506.5(F2):c.19T>C (p.Leu7=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2902313	NM_000506.5(F2):c.69C>T (p.His23=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2897604	NM_000506.5(F2):c.1437C>T (p.His479=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2896567	NM_000506.5(F2):c.210C>T (p.Ala70=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2895958	NM_000506.5(F2):c.79+10T>C	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2895957	NM_000506.5(F2):c.831C>T (p.Ala277=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2895136	NM_000506.5(F2):c.1597C>A (p.Arg533=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2894701	NM_000506.5(F2):c.1389T>C (p.Ile463=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2894390	NM_000506.5(F2):c.1725+9C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2894028	NM_000506.5(F2):c.560-6C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2894018	NM_000506.5(F2):c.105G>A (p.Arg35=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2893896	NM_000506.5(F2):c.265+8C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2893597	NM_000506.5(F2):c.80-9G>A	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2893444	NM_000506.5(F2):c.501C>T (p.Pro167=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2893436	NM_000506.5(F2):c.1449G>A (p.Leu483=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2892905	NM_000506.5(F2):c.342G>A (p.Thr114=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2892738	NM_000506.5(F2):c.228C>G (p.Ser76=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2892634	NM_000506.5(F2):c.801G>T (p.Gly267=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2892364	NM_000506.5(F2):c.1476G>A (p.Leu492=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2891697	NM_000506.5(F2):c.1678C>A (p.Arg560=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2891333	NM_000506.5(F2):c.265+9C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2891279	NM_000506.5(F2):c.594C>T (p.Arg198=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2891261	NM_000506.5(F2):c.549C>A (p.Ile183=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2890557	NM_000506.5(F2):c.1287C>T (p.His429=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2890535	NM_000506.5(F2):c.678G>A (p.Ala226=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2889777	NM_000506.5(F2):c.525C>T (p.Thr175=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2889538	NM_000506.5(F2):c.879G>A (p.Glu293=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2889143	NM_000506.5(F2):c.813C>G (p.Gly271=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2888253	NM_000506.5(F2):c.174A>G (p.Arg58=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2888085	NM_000506.5(F2):c.1227G>T (p.Leu409=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2887667	NM_000506.5(F2):c.1761C>T (p.Ile587=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2887590	NM_000506.5(F2):c.213C>T (p.Phe71=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2887406	NM_000506.5(F2):c.1116C>T (p.Ile372=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2887275	NM_000506.5(F2):c.597C>T (p.Ser199=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2886690	NM_000506.5(F2):c.216G>A (p.Glu72=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2886444	NM_000506.5(F2):c.265+10G>A	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2886435	NM_000506.5(F2):c.999G>A (p.Glu333=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2886358	NM_000506.5(F2):c.708C>T (p.Ala236=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2886351	NM_000506.5(F2):c.717C>T (p.Ser239=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2885530	NM_000506.5(F2):c.80-10C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2885313	NM_000506.5(F2):c.1806C>T (p.Phe602=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2885128	NM_000506.5(F2):c.1745G>A (p.Trp582Ter)	F2 (W582*)	Single nucleotide variant (nonsense)	Congenital prothrombin deficiency	GLikely pathogenic
Select item 2884938	NM_000506.5(F2):c.1302C>T (p.Tyr434=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2884837	NM_000506.5(F2):c.1413T>C (p.Pro471=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2884753	NM_000506.5(F2):c.1130+9T>C	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2884683	NM_000506.5(F2):c.108G>A (p.Ser36=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2884669	NM_000506.5(F2):c.582G>A (p.Ala194=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2884634	NM_000506.5(F2):c.648T>G (p.Asp216Glu)	F2 (D216E)	Single nucleotide variant (missense variant)	F2-related condition +1 more	GLikely benign
Select item 2884617	NM_000506.5(F2):c.627A>G (p.Pro209=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2884504	NM_000506.5(F2):c.392dup (p.Trp132fs)	F2 (W132fs)	Duplication (frameshift variant)	Congenital prothrombin deficiency	GPathogenic
Select item 2884216	NM_000506.5(F2):c.450C>T (p.Ala150=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2884152	NM_000506.5(F2):c.153G>A (p.Val51=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2884140	NM_000506.5(F2):c.279G>A (p.Ala93=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2883892	NM_000506.5(F2):c.558T>C (p.Cys186=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GUncertain significance
Select item 2883620	NM_000506.5(F2):c.933C>T (p.Ile311=)	F2	Single nucleotide variant (synonymous variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2881877	NM_000506.5(F2):c.1655-18C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2880344	NM_000506.5(F2):c.80-12A>C	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2880147	NM_000506.5(F2):c.1655-17G>A	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2880128	NM_000506.5(F2):c.1003+19G>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2879161	NM_000506.5(F2):c.1654+17C>G	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2877572	NM_000506.5(F2):c.316+15C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2876931	NM_000506.5(F2):c.1299-17T>C	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2875107	NM_000506.5(F2):c.1654+18G>A	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2875044	NM_000506.5(F2):c.240+17C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2874640	NM_000506.5(F2):c.559+12G>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign
Select item 2874332	NM_000506.5(F2):c.1654+17C>T	F2	Single nucleotide variant (intron variant)	Congenital prothrombin deficiency	GLikely benign

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